Guide for reporting to the National Pollutant Release Inventory 2025-2027
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Should any inconsistencies be found between this guide and the official Canada Gazette, Part I Notice with respect to substances in the National Pollutant Release Inventory for 2025, 2026 and 2027, published on March 8, 2025, the Notice will prevail.
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1. Introduction
The National Pollutant Release Inventory (NPRI) is Canada’s legislated, publicly accessible inventory of pollutant releases, disposals and recycling. Sections 46–53 of the Canadian Environmental Protection Act, 1999 (CEPA) contain information-gathering provisions that allow the Minister of Environment and Climate Change Canada to require reporting of information on substances. The provisions also require the Minister to establish and publish a national inventory of releases and transfers of pollutants. These provisions under CEPA form the primary legislative basis for the NPRI.
NPRI information is a major starting point for identifying and monitoring sources of pollution in Canada, and in developing indicators for the quality of our air, land and water. The NPRI helps determine if regulatory or other action is necessary to ensure reductions, and if so, the form that action should take. The NPRI provides Canadians with annual information on releases and transfers from industrial, institutional, commercial and other types of facilities in their communities.
The NPRI reporting requirements for the 2025-2027 reporting years were published in the Notice with respect to substances in the National Pollutant Release Inventory for 2025, 2026 and 2027 in the Canada Gazette, Part I, on March 8, 2025. This guide is designed to assist facility owners and operators in understanding the NPRI reporting requirements, and in determining if they are required to report to the NPRI. It provides a general overview of the reporting requirements for all NPRI substances, and provides information on additional guidance materials that address specific sectors, activities and substances.
The requirements described in this guide apply to the 2025, 2026 and 2027 calendar years. Note that facility owners or operators must consider each year individually when determining if thresholds are met and if reporting is required. Quantities of substances that are released, disposed of, and recycled should be reported by the specified deadline for each year.
2. Reporting deadlines and changes to reporting requirements
2.1 Reporting deadlines
Reporting is mandatory for facilities that meet the requirements of the NPRI Notice published in the Canada Gazette, Part I.
The deadline for reporting to the NPRI for the 2025 calendar year is June 1, 2026.
The deadline for reporting to the NPRI for the 2026 calendar year is June 1, 2027.
The deadline for reporting to the NPRI for the 2027 calendar year is June 1, 2028.
2.2 Changes to reporting requirements for 2025-2027
2.2.1 New requirements for reporting triarylmethane dyes
The following substances were added to Part 1, Group B, with a 100 kg manufactured, processed, or otherwise used (MPO) threshold and 1% concentration threshold for each substance:
- Basic Violet 3, Chemical abstract service registry number (CAS RN) 548-62-9
- Basic Violet 4, CAS RN 2390-59-2
- Basic Blue 7, CAS RN 2390-60-5
- MAPBAP Acetate, CAS RN 72102-55-7
C.I. Basic Green 4 (CAS RN 569-64-2) was deleted from Part 1, Group A, and added to Part 1, Group B, with an MPO threshold of 100 kg and 1% concentration threshold. C.I. Basic Green 4 was renamed Malachite Green.
2.2.2 New requirements for reporting benzothiazoles that can form 2-mercaptobenzothiazole
2-Mercaptobenzothiazole (CAS RN 149-30-4) was deleted from Part 1, Group A, of the substance list. A group of 20 benzothiazoles that can form 2-mercaptobenzothiazole (MBT) (see Appendix F for the full list of substance names and CAS RNs), including MBT, was added to Part 1, Group B, of the substance list with a 100 kg MPO threshold and a 0.1% concentration by weight threshold. The thresholds apply to the total of the 20 substances.
2.2.3 New requirements for reporting long-chain aliphatic amines
Ninety-two long-chain aliphatic amines (see Appendix F for full list of names and CAS RNs) were added to Part 1, Group B, of the substance list with an MPO threshold of 5,000 kg and a concentration threshold of 0.1% by weight. The thresholds apply to the total of the 92 substances.
2.2.4 New requirements for reporting hydrogen cyanide, free cyanide, cyanide salts and cyanide complexes
Free cyanide, cyanide salts and cyanide complexes were added to Part 1, Group B, of the NPRI substance list with a 1,000 kg MPO threshold and a 0.1% concentration by weight threshold. The thresholds apply to the total of the group of substances. Hydrogen cyanide (CAS RN 74-90-8) was deleted from Part 1, Group A, and added to Part 1, Group B, of the substance list with an MPO threshold of 1,000 kg and 0.1% concentration. See Appendix F for the full list of names and CAS RNs included in this substance grouping.
Please note that hydrogen cyanide (HCN) may be incidentally produced in significant quantities during high-temperature industrial processes, such as carbon black production, petroleum refining, and coke processing. These incidental by-products are required to be included in the ‘manufacture, process or otherwise use’ (MPO) threshold calculation and must be reported to NPRI if the 1,000 kg threshold is met. Concentration thresholds do not apply to by-products.
2.2.5 New requirements for reporting per- and polyfluoroalkyl substances
One hundred sixty-three per- and polyfluoroalkyl substances (PFAS) were added to a new Part 1, Group C, of the substance list. Facilities that meet the employee threshold and that MPO 1 kg or more of a listed PFAS at a concentration of 0.1% by weight or more will be required to report quantities of that PFAS that are released, disposed of and recycled. The mass and concentration thresholds apply to each listed PFAS individually. More information for reporting these substances can be found in section 5.4 of this Guide.
2.2.6 New requirements for reporting ethylene oxide
Ethylene oxide (CAS RN 75-21-8) was deleted from Part 1A and added to Part 1B of the NPRI substance list, with an MPO threshold of 1 kg and a 0.1% concentration. In addition, the reporting requirements for ethylene oxide now apply to activities related to the education and training of students.
2.2.7 Clarification of the definition for Naphthenic Acid Fraction Compounds (and their salts)
Changes were made to clarify the definition for naphthenic acid fraction compounds (and their salts). No changes were made to the reporting requirements for this substance. The definition found in the Canada Gazette is as follows:
Carboxylic acids that include chain compounds and compounds with one or more alicyclic ring structures with the general formula CnH2n+ZOxNαSβ, where “n” indicates the carbon number; “Z” is referred to as the “hydrogen deficiency” (the number of hydrogen atoms that are lost as the structures become more compact) and is zero or a negative, even integer (from -2 to -12); “x” refers to the oxygen number; “α” refers to the nitrogen number; and “β” refers to the sulphur number. Includes diverse polar organic compounds present in bitumen and oil sands process-affected water. This includes several compound classes, including aromatic, adamantine, or diamondoid structures, sulphur- and nitrogen-containing compounds, and oxygenated acids.
3. General information and overview of reporting requirements
3.1 Introduction
This section summarizes the process for reporting to the NPRI, describes the legal basis for the NPRI, provides an overview of the NPRI reporting requirements, provides definitions of terms that are used throughout the guide, and describes the information to be reported that applies to more than one group of substances. This section also provides information on additional resources that are available to assist in determining if a report is required for a facility, and on the methods for estimating quantities of releases, disposals and transfers for recycling. Details on reporting requirements and information to be reported that are specific to substances from Parts 1 through 5 are presented in sections 4 through 9.
3.2 Process for reporting to the NPRI
An NPRI report can be created and submitted to Environment and Climate Change Canada using the online reporting system. Step-by-step instructions for creating and submitting a report are available in the online reporting system and on the NPRI website.
The owner/operator of a facility must review the specific reporting requirements applicable to their facility to determine if they are required to report to the NPRI. If the requirements are met, then the total quantities of NPRI substances released, disposed of, and transferred for recycling must be reported to the NPRI using the online reporting system, even if the total quantity is zero.
A facility that submitted a report in the previous year but no longer meets NPRI reporting criteria for the current year, is required to submit a “Does Not Meet Criteria (DNMC)” report using the online system by the reporting deadline.
The NPRI reporting process is outlined below:
- Option one: the facility meets reporting requirements for the reporting year:
- estimate the quantities of all applicable pollutant categories for the facility for the reporting yea
- submit an NPRI Report in the Single Window Information Manager (SWIM)
- submit a Sales/Closure/Purchase Report in SWIM, if applicable
- keep a record of all information and backup calculation files
- Option two: the reporting requirements are not met but the facility was sold/closed/purchased during the reporting year:
- submit a Sales/Closure/Purchase Report in SWIM
- keep a record of all information and backup any files
- Option three: the reporting requirements are not met, and the facility was not sold/closed/purchased during that reporting year:
- if an NPRI report was submitted the previous year, submit a Does Not Meet Criteria Report and keep a record of all information
- if no report was submitted the previous year, no reporting is required
3.3 The Canada Gazette Notice – The legal basis for the NPRI
The legal basis for the NPRI is the Notice with respect to substances in the National Pollutant Release Inventory for 2025, 2026 and 2027 published in the Canada Gazette, Part I (hereafter referred to as “the Notice”). The Notice is published under the authority of subsection 46(1) CEPA. It specifies that any person who owned or operated a facility during the 2025, 2026 or 2027 calendar years, under the conditions prescribed in the Notice, must provide certain information to the Minister of the Environment and Climate Change by the reporting deadline for that calendar year.
Reporting to the NPRI is mandatory. Companies that meet reporting requirements but fail to report, fail to report on time, or knowingly submit false or misleading information, face penalties as listed under section 272 of CEPA. Facilities that did not meet the reporting criteria or were exempt from reporting in previous years should review their status to determine whether they are required to report each year.
The owner or operator of the facility as of December 31st of the given year is required to report to the NPRI, whether or not the ownership of the facility changes during the calendar year. If operations at a facility are terminated, the last owner or operator of the facility is required to report. An NPRI report may need to be submitted for a facility that is under decommissioning or in care or maintenance mode if the employee and/or substance-specific reporting criteria are met. Once reporting criteria are met for a substance, an NPRI report must be submitted for that substance regardless of the quantities released, disposed of, or transferred (even if the quantity is zero).
The Notice encompasses a wide range of substances and groups of substances (available on the NPRI website in HTML and MS ExcelTM formats), reporting criteria and requirements. It is divided into four schedules with several parts in each:
- list of substances:
- Part 1 lists 373 substances and groups of substances and is divided into groups A, B, and C, based on thresholds and information to be reported (referred to as Part 1A, Part 1B, and Part 1C substances)
- Part 2 lists 31 individual polycyclic aromatic hydrocarbons (PAHs)
- Part 3 lists 7 dioxins, 10 furans and hexachlorobenzene (HCB)
- Part 4 lists 7 criteria air contaminants (CACs)
- Part 5 lists 62 selected volatile organic compounds (VOCs) and groups of VOCs with additional reporting requirements (speciated VOCs)
- definitions:
- provides definitions of the terms used in the Notice
- reporting criteria:
- general reporting criteria, including the reporting deadline, the employee threshold, and exclusions and exemptions
- Parts 1-5 provides criteria for substances listed in the corresponding Schedule 1 Part
- information to be reported:
- general information required to be reported and manner of reporting
- information to be reported on the facility, including name, identification codes, contacts and pollution prevention activities
- Parts 1-5 provide information to be reported for substances listed in the corresponding Schedule 1 Part
3.4 Key concepts for understanding NPRI reporting requirements
This section is designed to help facility owners and operators understand the NPRI reporting requirements and determine if they are required to report to the NPRI. The following sections give a brief overview of the NPRI reporting requirements, the substance list, the employee threshold, and other key definitions. Additional definitions for terms used in this guide can be found in the Glossary.
3.4.1 Facilities to which the NPRI reporting requirements apply
In general, an NPRI report is required for any facility:
- where employees work a total of ≥ 20,000 hours (the employee threshold) (see section 3.4.3)
- where specified activities to which the employee threshold does not apply take place (see section 3.4.3)
- where the reporting criteria for CACs are met, whether or not the employee threshold is met
- that is a pipeline installation (defined in section 3.4.2)
- that is subject to the Chromium Electroplating, Chromium Anodizing and Reverse Etching Regulations
In addition, the facility must meet any of the other reporting criteria (e.g., mass, concentration or activity thresholds) for substances on the NPRI substance list.
3.4.2 Definition of facility
The term “facility” refers to a contiguous facility, a portable facility, a pipeline installation or an offshore installation, as defined below. The different types of facilities have to consider different subsets of the NPRI substance list: contiguous facilities and offshore installations need to consider the substances in all Parts of the substance list; portable facilities need to consider substances in Parts 2-5; and pipeline facilities need to consider only Part 4 and 5 substances. See section 3.4.4 for more information on the Parts of the NPRI Substance list.
- Contiguous facility
- A contiguous facility is defined as all buildings, equipment, structures and stationary items that are located on a single site, or on contiguous sites or adjacent sites, that are owned or operated by the same person and that function as a single integrated site, including wastewater collection systems that release treated or untreated wastewater into surface waters.
- Portable facility
- A portable facility is defined as portable polychlorinated biphenyl (PCB) destruction equipment, portable asphalt plants and portable concrete batching plants. The definition applies where the facility can be entirely relocated for operation. The owner or operator of a portable facility must submit a report for the location where the facility operated for the longest period of time in the calendar year, using the total quantity of releases, disposals, or transfers from all operating locations. For all other locations where the portable facility operated during the year, the dates, addresses and geographic coordinates are to be submitted in the facility comments section in the online reporting system.
- Pipeline installation
- A pipeline installation is defined as a collection of equipment, situated at a single site, used in the operation of a natural gas transmission or distribution pipeline. This definition includes pipeline compressor and storage stations along pipelines used to transport raw or processed natural gas.
- Offshore installation
- An offshore installation is defined as an offshore drilling unit, production platform or ship, or subsea installation that is related to the exploitation of oil or natural gas and that is attached or anchored to the continental shelf of Canada or within Canada’s exclusive economic zone.
3.4.3 The employee threshold
Facilities where the employees work a total of 20,000 hours or more during the calendar year (the employee threshold) are required to report to the NPRI, if the thresholds for at least one substance are met, or if an activity-based threshold is met. The employee threshold depends on the number of hours worked by all employees at the facility during the calendar year. This includes:
- all hours worked by individuals employed at the facility, regardless of function or location, including students, part-time and term employees
- all hours worked by the owner(s) who performed work on-site at the facility
- all hours worked by a person, such as a contractor, who performed work at the facility that is related to the operations of the facility
- all paid overtime, vacation and sick leave
The employee threshold must be met by most facilities before they need to consider reporting for Parts 1 through 3 substances, unless activities to which the employee threshold does not apply take place at the facility.
Activities to which the employee threshold does not apply
If one or more of the following activities take place at the facility and other reporting criteria such as mass and concentration thresholds are met, the owner/operator of the facility must report to the NPRI regardless of the number of hours worked by employees:
- non-hazardous solid waste incineration of ≥ 26 tonnes of waste, including, but not limited to, conical burners and beehive burners
- biomedical or hospital waste incineration of ≥ 26 tonnes of waste
- hazardous waste incineration
- sewage sludge incineration
- wood preservation (using heat or pressure treatment, or both)
- terminal operations
- discharge of treated or untreated wastewater from a wastewater collection system discharging an average of ≥ 10,000 m3/day into surface waters
- production of ≥ 500,000 tonnes at pits or quarries
The employee threshold does not apply to facilities where these activities occur because these activities release significant quantities of NPRI substances to the environment, while not necessarily employing enough people to meet the threshold. Detailed descriptions of these activities are provided in the Glossary.
Facilities that are subject to the Chromium Electroplating, Chromium Anodizing and Reverse Etching Regulations are required to report releases, disposals, and transfers for recycling of hexavalent chromium (and its compounds), regardless of the number of employees and regardless of the 50 kg NPRI threshold.
3.4.4 The NPRI substance list: Parts 1-5
The NPRI substance list is divided into five parts, based on specific reporting criteria for each part. The reporting thresholds may be based on mass, concentration, or specific activities and are explained in detail in sections 5 through 9 of this guide. Table 1 provides an overview of the reporting requirements for each Part of the substance list.
Definitions for the manufacture, process, or otherwise use of a substance are found in the Glossary and are further explained in section 5 of this guide.
| Part | Substances | Mass threshold | Reporting thresholds |
|---|---|---|---|
| 1A | 177 substances and groups of substances | 10 tonnes | Total of the quantities of a substance:
|
| 1B | 33 substances and groups of substances | 1 to 1,000 kg, depending on the substance | Total of the quantities of a substance:
|
| 1C | 163 per- and polyfluoroalkyl substances (PFAS) | 1 kg | Total of the quantities of a substance:
|
| 2 | 31 polycyclic aromatic hydrocarbons (PAHs) | 50 kg | Total of the quantities of PAHs at any concentration:
|
| 2 | 31 polycyclic aromatic hydrocarbons (PAHs) | Any quantity | Where wood preservation using creosote takes place, all releases, disposals and transfers for recycling must be reported, regardless of quantities or concentrations |
| 3 | 7 dioxins, 10 furans, and hexachlorobenzene | Any quantity | Where specified activities take place, reporting is mandatory regardless of quantities or concentrations |
| 4 | carbon monoxide, nitrogen oxides, sulphur dioxide, and total particulate matter | 20 tonnes | Quantity released to air (no concentration threshold applies) |
| 4 | volatile organic compounds (VOCs) | 10 tonnes | Quantity released to air (no concentration threshold applies) |
| 4 | particulate matter ≤ 10 micrometres (PM10) | 0.5 tonnes | Quantity released to air (no concentration threshold applies) |
| 4 | particulate matter ≤ 2.5 micrometres (PM10) | 0.3 tonnes | Quantity released to air (no concentration threshold applies) |
| 5 | 62 speciated VOCs (individual VOCs, isomer groups and other groups and mixtures) | 1 tonnes | Quantity released to air (no concentration threshold applies) |
3.4.5 Releases, disposals and transfers
Once it has been determined that a facility meets the specific thresholds for an NPRI substance, the total quantities released, disposed of, or transferred must be reported.
The NPRI has four main categories reportable to the NPRI. Detailed definitions for each of the reportable categories can be found in the Glossary.
- On-site releases
-
- air:
- stack or point releases
- storage tank and related handling releases
- fugitive releases
- spills or other accidental releases
- unpaved road dust
- other non-point releases
- surface waters:
- direct discharges
- spills
- leaks
- land:
- spills
- leaks
- other releases to land that are not disposals
- On-site disposals
-
- landfill
- land application
- underground injection
- tailings and waste rock
- Off-site transfers for treatment and disposal
-
- treatment prior to final disposal:
- physical
- chemical
- biological
- incineration or thermal where energy is not recovered
- in a municipal wastewater treatment plant
- off-site disposals:
- landfill
- land application
- underground injection
- storage off-site prior to final disposal
- tailings and waste rock
- Off-site transfers for recycling and energy recovery
-
- energy recovery
- recovery of solvents
- recovery of organic substances (not solvents)
- recovery of metals and metal compounds
- recovery of inorganic materials (not metals)
- recovery of acids or bases
- recovery of catalysts
- recovery of pollution abatement residues
- refining or reuse of used oil
- other recovery, reuse or recycling activities
3.5 Exemptions from and exclusions to NPRI reporting requirements
3.5.1 Facilities exempt from all reporting requirements
NPRI reporting requirements do not apply if the only activities that take place at a facility are:
- exploration for oil or gas, or the drilling of oil or gas wells
- discharge of treated or untreated wastewater from a wastewater collection system with an average discharge of < 10,000 m3 per day into surface waters
- production of < 500,000 tonnes at pits or quarries
- open-pit mines are not included in the definition of a pit or quarry (see the Glossary) and are subject to NPRI reporting requirements
3.5.2 Exclusions for all substances
The quantity of a substance contained in any of the following items should not be included when calculating if the reporting threshold was met and when calculating and reporting releases, disposals or transfers for recycling:
- Articles that are processed or otherwise used
- an article is defined as a manufactured item that does not release an NPRI substance when it undergoes processing or other use (see the Glossary for examples)
- materials used as structural components of the facility (buildings and other fixed structures), but not process equipment
- materials used in janitorial or facility grounds maintenance
- this includes:
- NPRI substances contained in fertilizers and pesticides used for grounds maintenance
- cleaning agents used for maintaining facility cleanliness
- paint used for building maintenance.
- the maintenance of process equipment (e.g., painting or cleaning manufacturing equipment with a solvent) is not excluded
- this includes:
- materials used for personal use by employees or other persons
- intake water or intake air such as:
- water used for process cooling
- air used either as compressed air or for combustion
The quantity of a substance that is manufactured, processed or otherwise used in the exploration for oil or gas or in the drilling of oil or gas wells should not be included when calculating if the reporting threshold was met and when calculating and reporting releases, disposals or transfers for recycling. This exclusion applies to all activities from initial exploration until the well is put into production.
In addition, vehicle emissions (not including unpaved road dust) should not be considered when calculating if the thresholds were met and when reporting releases, disposals or transfers for recycling. A vehicle is any mobile equipment that is capable of self-propulsion, including fleet vehicles and earth moving equipment (e.g., loaders, dump trucks, forklifts, excavators and bulldozers).
3.5.3 Activities exempt from reporting for Parts 1-3 substances
The threshold calculation for a substance must exclude the quantity of a substance that is manufactured, processed or otherwise used in the following activities:
- education or training of students (for example, universities, colleges and schools), except when considering whether the threshold is met for reporting releases of ethylene oxide (CAS RN 75-21-8)
- research or development
- maintenance and repair of vehicles (automobiles, trucks, locomotives, rail cars, ships or aircraft), except painting and stripping of vehicles or their components, or the rebuilding or remanufacturing of vehicle components
- substances used for routine, scheduled and preventative maintenance of vehicles are exempt (e.g., repair, cleaning, replacement of lubricants/fluids)
- substances used in the painting or stripping of vehicles or vehicle components are subject to reporting
- there is no exemption for activities that involve the removal, breakdown and total reconstruction of vehicle components (e.g., engines, landing gear, traction motors) using recovered or new parts, such that the rebuilt component is reinstalled or sold as an as-new replacement
- distribution, storage or retail sale of fuels, except as part of terminal operations (defined in the Glossary)
- the exemption for distribution, storage or sale of fuels does not include terminal operations
- wholesale or retail sale of the substance or articles or products that contain the substance.
- materials or substances sent back to a manufacturer, supplier or recycler for reprocessing, repackaging, resale or for credit or payment are considered to be recycled, and the exemption for wholesale or retail sale does not apply
- growing, harvesting or management of renewable natural resources
- the practice of dentistry
A facility is exempt from reporting Parts 1 through 3 substances if the only source or use of that substance is from one or more of the activities listed above. Note, however, that these facilities are not exempt from reporting releases of Parts 4 and 5 substances from stationary combustion equipment.
In cases where a facility met the reporting criteria for a substance based on sources other than those listed above, the quantity of that specific substance from any exempt activities should also be excluded when reporting releases, disposals or transfers for recycling to the NPRI. As of the 2025 reporting year, the exemption for the quantity of a substance that is manufactured, processed, or otherwise used in the education or training of students no longer applies when reporting releases of ethylene oxide (CAS RN 75-21-8).
3.5.4 Exclusions for tailings and waste rock
The following sections describe the exclusions for unconsolidated overburden, inert waste rock and stable/inert constituents of tailings. Refer to the Glossary for definitions of tailings and waste rock. These exclusions apply only to substances contained in tailings and waste rock. If a substance is released to air or water from tailings or waste rock (e.g., in airborne dust or as effluent), the quantity of the substance released must be included in threshold calculations.
Unconsolidated overburden
Substances contained in unconsolidated overburden should be excluded from threshold calculations and reporting. Unconsolidated overburden is unconsolidated materials overlying the ore or bitumen deposit, including, but not limited to, soil, glacial deposits, sand and sediment.
Inert waste rock
Substances contained in inert or clean waste rock should be excluded from threshold calculations and reporting. Inert waste rock is defined as waste rock either:
- is inert or clean according to a federal or provincial operating permit
- has a sulphur concentration of ≤ 0.2%
- has a sulphur concentration of > 0.2%, and the ratio of neutralizing potential to acid generating potential is ≥ 3:1
There is one exception to the exclusion for inert or clean waste rock: even if waste rock is inert or clean as defined above, the quantity of arsenic in waste rock cannot be excluded if the concentration of arsenic is > 12 milligrams per kilogram of waste rock.
Stable/inert constituents of tailings
Substances contained in certain materials in tailings should be excluded from threshold calculations and reporting (e.g., sand grains from bitumen mines or in-situ production of bitumen). In order to be excluded, these materials must:
- be inert
- be inorganic
- not have been crushed or otherwise physically or chemically altered
The exclusion applies only to the components of tailings that meet the above three criteria (i.e., if part of the tailings stream met the criteria, only that portion of the tailings would be excluded, and the remainder of the tailings would be included).
3.6 Methods for estimating quantities of NPRI substances
3.6.1 Reasonable access to information
Information on releases, disposals and transfers for recycling needs to be reported if the owner/operator possesses the information or may reasonably be expected to have access to the information. The Notice specifies that if emissions are already monitored or measured under provincial or federal legislation or a municipal bylaw, those measurements must be used to report to the NPRI. However, all releases, disposals or transfers off site for recycling must be included in threshold calculations and reported, unless otherwise specified, not just those that are measured or monitored.
An NPRI report is mandatory for any substances that meet the reporting thresholds, regardless of whether the substance is being measured or monitored for other jurisdictions. If emissions are not monitored or measured under provincial or federal legislation or a municipal bylaw, reasonable efforts must still be undertaken to gather information on releases, disposals and transfers of a substance. What is “reasonable” depends on individual circumstances, but may include additional measures (e.g., additional monitoring, contacting suppliers, conducting source testing) for NPRI substances.
Other measures that may assist a facility in reporting to the NPRI include:
- requesting detailed composition data from suppliers
- while some manufacturers may cite proprietary restrictions, others may be able to provide the information when regulatory obligations are cited
- using publicly available data sources such as peer-reviewed literature, information from the United States Environmental Protection Agency, or industry-specific studies to make estimates
- applying surrogate or comparable data where appropriate
- reasonable estimates based on similar facilities, analogous processes, or comparable substances may be used when specific data is not accessible
- applying expert judgement in the absence of specific data, drawing on knowledge of the chemical and physical processes, the design and operation of the equipment or system, and relevant physical and chemical principles
In deciding whether additional efforts should be undertaken to generate new information for the purposes of NPRI reporting, the following factors, among others, should be considered:
- the health and environmental risks posed by a substance, including whether the substance has been declared toxic under CEPA
- the relative contribution of the industrial sector or the facility to releases, disposals and transfers for recycling of a substance in Canada
- the cost of additional monitoring
3.6.2 Bases of estimate that can be used to report to NPRI
Estimates of the quantity of a substance that is manufactured, processed or otherwise used, and of the quantity that is released, disposed of or transferred for recycling, may be based on one of the following methods:
- continuous emission monitoring systems (reporting system code M1)
- predictive emission monitoring (M2)
- source testing (M3)
- remote quantification (RQ)
- mass balance (C)
- site-specific emission factor (E1)
- published emission factor (E2)
- speciation profile (SP)
- engineering estimates (O)
The reporting system only allows one basis of estimate for each individual type of release, disposal and transfer. If more than one basis of estimate is used to arrive at a single quantity to be reported, select the basis of estimate that was used to calculate the majority of the value. Further explanation on the basis of estimate used can be provided in the comment fields found on the main pages for reporting releases, disposals and recycling in the online reporting system.
A description of these methods is provided in the following sections. Examples using these estimation methods can be found in Appendix B.
Note that facilities can choose the most appropriate basis of estimate to report to the NPRI based on their particular circumstances. However, if the facility is required by federal or provincial legislation or a municipal by-law to measure or monitor releases, disposals or transfers for recycling, the facility must use those data to report to the NPRI.
- Continuous emission monitoring systems
- Continuous emission monitoring systems (CEMS) record emissions over an extended and uninterrupted period. Once the concentration of a substance and the total flow rate of the stream being measured have been determined, emission rates can be calculated by multiplying the concentration by the discharge flow rate or volumetric stack gas flow rate. Annual emissions of the substance can then be estimated by multiplying the concentration by the annual flow rate of the discharged effluent or the gases in the stack or duct.
- Predictive emission monitoring
- Predictive emission monitoring (PEM) is based on developing a correlation between substance emission rates and process parameters (e.g., fuel usage, steam production, furnace temperature). PEM may be considered a hybrid of continuous monitoring, emission factors and stack tests. A correlation test must first be performed to determine the relationship between emission rates and process parameters. Emissions can then be calculated or predicted using process parameters to predict emission rates based on the results of the initial source test.
- Source testing
-
Source testing involves collecting a sample of the emission or effluent, then determining the concentration of one or more substances in the sample. The concentration of the substance(s) of interest is then multiplied by the volumetric flow rate to determine the quantity of the substance(s) emitted over time.
Source testing of air emissions generally involves inserting a sampling probe into the stack or duct to collect a volume of exhaust effluent isokinetically. The substances collected in or on various media are subsequently analyzed. For liquid effluents, grab samples or composite samples are extracted from the effluent stream.
- Remote quantification
-
Remote quantification, or optical remote sensing (ORS) methods, are measurement methods that are conducted away from the point or area where a pollutant is emitted. ORS methods measure the concentration of air pollutants based on their interaction with electromagnetic radiation (i.e., ultraviolet, visible or infrared light). Examples include:
- differential absorption lidar (DIAL)
- differential optical absorption spectroscopy (DOAS)
- Fourier-transform infrared spectroscopy (FTIR)
- solar occultation flux (SOF)
- tunable diode laser (TDL)
- Mass balance
-
Mass balance involves applying the law of conservation of mass to a facility, process or piece of equipment. If there is no accumulation, all the materials that go into the system must come out. Releases are determined from the differences in input, output, accumulation and depletion of a substance. The general equation for a mass balance is:
Where:
- Min = Mass of compound in the raw material feed
- Mout = Mass of compound in the finished product and released to air, land and water (Mout = Mproduct + Memitted)
- Maccumulated/depleted = Mass of compound accumulated or depleted in the system
The reliability of release estimates based on mass balances is dependent on the source type considered. Mass balance methods may be preferred for some releases, such as solvent use and loss. This method may not be suitable for many other sources, such as cases where chemical transformation of input streams occurs.
- Site-specific and published emission factors
-
Generally, emission factors relate the quantity of substances emitted from a source to a common activity associated with those emissions. Emission factors may be published or developed by facilities using emission testing data and source-activity information. For a particular piece of equipment, specific emission factors may be available from the manufacturer or sales centre. The basic equations for determining emissions from emission factors are as follows:
Where:
- Ex = Emission of substance × (kg or other unit of mass)
- A = Activity rate
- EF= Emission factor
Care should be taken when using published emission factors, as some emission factors may be out of date or underestimate releases. Before using emission factors, facilities should find the most appropriate emission factors for their operations; ensure that they are as up-to-date as possible; and verify that they reflect actual emissions, particularly in cases where emission factors have been known to underestimate releases.
- Speciation profile
- Speciation profiles provide estimates of the chemical composition of emissions, and are used to disaggregate substance quantities (e.g., total VOCs and PM) into more detailed species (e.g., individual VOCs and PM fractions). Speciation profiles may be published (e.g., the US Environmental Protection Agency’s SPECIATE 5.4 database), or developed for site-specific use.
- Engineering estimates
-
In many cases, sound engineering assessment is the most appropriate approach to determining process factors and base quantity values. Releases can be estimated from engineering principles and judgement by using knowledge of the chemical and physical processes involved, the design features of the source, and an understanding of the applicable physical and chemical laws. The reliability of these estimates depends on the complexity of the process and the level of understanding of its physical and chemical properties.
To apply an engineering assessment method, follow these four basic principles:
- review all data pertaining to the specific source and to the industrial sector in general
- use this data to provide gross approximations
- refine the approximations using sound engineering principles as data become available, in order to provide more accurate estimations
- whenever possible, use alternate methods of calculation to cross-check each level of approximation
- employ good record keeping
3.6.3 Method detection limit and use of non-detect values
In NPRI reporting, the issue of measurements below the method detection limit (MDL) arises in several situations. The MDL is the smallest concentration of the substance under analysis (i.e., the analyte) that produces an instrumental response different from background levels, for a given test method and that meets all analyte detection and identification criteria of the specified test method. An indication that a reportable substance is below the MDL is not equivalent to stating that the substance is not present. If there is reason to believe that the substance is present based on input materials and processes, a value of half the MDL should be used to estimate the release.
In a year where multiple measurements of the concentration of a substance in a given process stream are all below the MDL, and there is no other reason to believe that the substance is present, it can be assumed that the concentration of the substance in that process stream is zero.
In a year where multiple measurements are taken, and some measurements indicate that the concentration is above the MDL and some indicate that it is below the MDL, there is reason to assume that the substance is present. Therefore, the mean value of all detectable and non-detectable measurements is recommended to be used.
3.6.4 Other guidance documents and tools
Environment and Climate Change Canada, the U.S. Environmental Protection Agency (US EPA), and industry associations provide resources to complete threshold calculations and to estimate releases, disposals and transfers for recycling of NPRI substances. These resources can be accessed through the NPRI Toolbox. Useful information can also be found in Safety Data Sheets, and in permits and certificates of approval.
The NPRI Toolbox includes a number of tools:
- general guidance
- emission calculation references
- information on fuel combustion and fugitive emission sources
- sector-specific resources
- substance-specific guidance
- additional guidance and resources
4. Information to be reported
4.1 Facility information
4.1.1 General facility information
Below summarizes the general information that must be provided for all facilities that report to the NPRI. Other facility information may also be required, depending on the type of facility and the substances reported.
Facility name and location
- name of the facility
- address of the physical location of the facility such as:
- a civic address
- a legal land description
- a description if no other type of physical address is applicable [e.g., for an offshore installation])
- latitude and longitude coordinates of the facility if the facility is reporting for the first time or if the facility is portable
Employees
Number of full-time employee equivalents, obtained by dividing by 2,000 hours the sum of:
- the total hours worked by individuals employed at the facility and the total hours of paid vacation and of sick leave taken by individuals employed at the facility
- the hours worked on-site at the facility by the owner of the facility, if not employed by the facility
- the hours worked on-site at the facility by a person, such as a contractor, who, at the facility, performs work related to the operations of the facility
Organization (company)
- legal and trade name of the facility’s company
- mailing address
- Dun & Bradstreet (D-U-N-S) numberFootnote 1
- federal business numberFootnote 2
Parent Companies (if any)
The parent company is the highest level company or group of companies that owns or directly controls the reporting facility. The parent companies of interest to NPRI are those Canadian companies that have greater than 10% ownership in the company.
- legal names of any Canadian parent companies and their percentage of ownership
- civic addresses of the parent companies
- D-U-N-S numbers of the parent companiesFootnote 1
- federal business numbers of the parent companiesFootnote 2
North American Industry Classification System (NAICS) Canada 2022 code
NAICS is an industry classification system developed by the statistical agencies of Canada, Mexico and the United States. Report the primary six-digit NAICS Canada code of the facility and the secondary and tertiary codes, if applicable.
4.1.2 Identification numbers
Environment and Climate Change Canada identification numbers
The NPRI identification number is a unique identifier provided by Environment and Climate Change Canada that must be used when reporting to the NPRI.
Where applicable, the Greenhouse Gas Reporting Program identification number must also be reported.
Provincial identification numbers for oil and gas facilities
Facilities classified as NAICS 211110 [Oil and gas extraction (except oil sands)] must report all provincial license or identification numbers (e.g., Petrinex numbers) associated with their NPRI identification number.
Petrinex is a joint strategic organization supporting Canada’s upstream, midstream and downstream petroleum industry and is currently represented by the Alberta Department of Energy (DOE), the Alberta Energy Regulator (AER) and the Saskatchewan Ministry of the Economy (ECON), and industry [represented by the Canadian Association of Petroleum Producers (CAPP) and The Explorers and Producers Association of Canada (EPAC)]. The Petrinex identification number is four letters followed by seven numbers.
If a facility in NAICS 211110 does not have a Petrinex ID number, a provincial facility licence number or other provincial or territorial identification number must be reported.
Other provincial or territorial identification numbers
Facilities are required to indicate any relevant provincial or territorial facility identification numbers (or “identifiers”), such as permit numbers. The requirement is limited to identifiers that are issued by the province or territory, with the exception of facilities in Metro Vancouver, where British Columbia has delegated responsibility for issuing operating permits to the Metro Vancouver Regional District. Required identifiers are those that apply at the facility level, as opposed to identifiers for specific equipment.
There are two broad categories of unique facility identifiers that may need to be reported:
- identifiers that relate to operating conditions/restrictions on environmental releases from the facility
- typically the “operating permit” of the facility, which can also be referred to as the approval, authorization, license or certificate
- these can also be unique identifiers that relate to operating conditions/restrictions outside of the “operating permits,” such as identifiers issued under specific Regulations, Codes of Practice or other non “operating permit” restrictions
- identifiers that relate to the reporting of environmental data
- for example, identifiers issued by provincial air emissions inventories of criteria air contaminants or greenhouse gases
Facilities can opt to report additional identifiers that do not fall within the first two categories, if those identifiers can provide added context to reported releases, disposals and recycling.
Applicable identification numbers will vary depending on the province or territory. Identifiers are generally 4 to 12 alphanumeric characters and may contain special characters (e.g., “-” or “/”). Identifiers can change over time for a wide range of reasons, e.g., renewal, amendment or change of ownership. Updated numbers should be reported.
Specific provincial/territorial programs/initiatives could have more than one facility identifier for each unique NPRI facility or there may be more than one NPRI facility associated with one unique facility identifier under a specific provincial/territorial program/initiative. All unique facilities identifiers must be reported, even if the NPRI-defined facility is only part of a facility as defined by the permitting agency.
The list below provides some information on provincial programs which may apply to the facility and on which identification numbers should be reported to the NPRI. It does not list all possible programs that could apply; it only presents the most common. Facilities should also consider other identification numbers that may need to be reported.
The information provided below is based on responses by the provinces to a survey conducted in late 2020. For the most up-to-date information, please refer to provincial/territorial web pages or contact your provincial/territorial government departments.
British Columbia
- Environmental Management Act waste discharge or air discharge permit, approval, operational certificate, regulation or code of practice
- Identifiers are numeric
- Metro Vancouver Regional District (MVRD) permit or approval
- MVRD identifiers are a mix of numbers and letters
- a permit identifier is “GVA” followed by unique four-digit number (e.g., GVA0001)
- an approval identifier is “GVU” followed by unique four-digit number (e.g., GVU0001)
Alberta
- Environmental Protection and Enhancement Act (EPEA) approval and EPEA Code of Practice
- EPEA approval and Code of Practice registration numbers are whole numeric values (with values ranging from 1 to approximately 424245)
- these ID numbers can range from one to six digits, but could potentially be more than six digits in the future
- this applies to facilities that report air releases of Part 4 substances or hydrogen sulphide to the NPRI
- Alberta Energy Regulator (AER)
- AER facility identifiers are alphanumeric (e.g., ABOS00555555) and only apply to facilities in NAICS 21, 22, and 32
- this may also be known as the Petrinex facility identifier.
Saskatchewan
- The Environmental Management and Protection Act and the Environmental Management and Protection (General) Regulations
- Identifiers are alphanumeric (e.g., Approval to Operate Pollutant Control Facilities PO20-132 would be the 132nd approval issued in the year 2020; Permit to Construct Industrial Waste Works PC19-034 would be the 34th permit to construct issued in 2019)
- The Mineral Industry Environmental Protection Regulations
- for sites that are subject to the Industrial Source Air Quality (ISAQ) chapter of the Saskatchewan Environmental Code, an Environmental Protection Permit (EPP) is issued with a 9-digit number identifying the submission of the application (e.g., 10022731)
- Hazardous Materials and Impacted Sites (HMIS)
- HMIS approval/permit identifiers are the year, followed by the district, followed by the next in sequence (e.g., 20-15-00001 would be 20 for the year 2020, 15 for the 15th district, and 0001 for the 1st in the sequence)
Manitoba
- Environment Act
- an Environment Act Licence has a 4-digit number that is issued under the Environment Act (e.g., 1234)
- when a licence is revised, it gets a suffix of letter “R” (e.g., 1234 R)
- the letter “R” is added every time a licence is revised (e.g., “RR”, “RRR”, etc.)
- with many changes it is shortened as “6R” or “7R”
- In the event a licence is altered due to an appeal, then the suffix will be a letter “E” (e.g., 1234 E)
- Dangerous Goods Handling and Transportation Act
- Dangerous Goods Handling and Transportation Act licence issued under The Dangerous Goods Handling and Transportation Act is a 3-digit number followed by “HW” (e.g., 123 HW)
- If a licence is revised it follows the same procedure as in the Environment Act licence
- Hazardous Waste Regulation
- Hazardous waste generator registration issued as per the Hazardous Waste Regulation
- this has two registration numbers - one for generators and the other for receivers
- It has five digit numbers prefixed with three letters and written as follows:
- Consignor (Generator) Registration No.: MBG12345
- Consignee (Receiver) Registration No.: MBR12345
- Water and Wastewater Facility Operators Regulation
- Water and Wastewater Facility Operators Regulation certification numbers are numeric (e.g., 2006-123)
Ontario
- Environmental Protection Act environmental compliance approval
- environmental compliance identifiers are four numeric characters followed by 6 alphanumeric digits (e.g., 9473-953Q2Q)
- older identifiers can be a string of numbers separated by dashes, or a series of numbers following a letter (e.g., 1-234-56-789, A123456 or W123456)
- Environmental Activity and Sector Registry (EASR)
- EASR numbers are one letter followed by 14 digits and contain dashes (e.g., R-001-0000000001)
Quebec
- Loi sur la qualité de l’environnement autorisation environnementale
- 9-digit number
- Québec Air Emissions Inventory (IQEA) under the Regulation Respecting the Mandatory Declaration of Certain Emissions of Contaminants into the Atmosphere (RDOCECA)
- IQEA facility identification numbers can be 8 numbers or an “X” or “Y” followed by 7 digits
New Brunswick
- New Brunswick Air Quality Regulation approval and New Brunswick Water Quality Regulation approval
- identifiers are alphanumeric (e.g., I-12345, S-1234)
Nova Scotia
- Nova Scotia Environment Act industrial, municipal, on-site sewage disposal or water approval
- approval identifiers are 10 to 11 digits, with the first four digits being the year in which the permit was issued with another 6 to 7 following the year (e.g., 2015-092352)
- some identifiers may have an additional 3 alphanumeric characters at the end, preceded by a “-“ (e.g., 2006-052877-T01, 2004-039856-R01)
Prince Edward Island
- Air Quality Regulations approval
- approval numbers can be numeric or alphanumeric (e.g., INC20455)
- Sewage Disposal Systems Regulations approval
- approval numbers can be numeric or alphanumeric (e.g., INC20455)
- Boiler and Pressure Vessels Act Regulations licence number
- license numbers are up to 6 alphanumeric characters (e.g., PL-C-195 or PL-089)
- Power Engineering Act Regulations license number
- license numbers are up to 6 alphanumeric characters (e.g., PL-C-195 or PL-089)
Newfoundland and Labrador
- Newfoundland and Labrador Environmental Protection Act Certificates of Approval for the Construction and/or Operation of industrial approvals
- the identifier is in the form “AAYY-MMXXXXO” where:
- “AA” is AA
- “YY” is the 2 digit year
- “MM” is the 2-digit month
- “XXXX” is the 4 digit sequential counter
- “O” is the optional for revisions
- e.g. AA18-085652A is the permit dated August 2018, it is sequentially number 5652, and is the first revision (A)
- the identifier is in the form “AAYY-MMXXXXO” where:
Yukon
- Air emissions permit
- 9-digit number with 2 hyphens (e.g., 4201-60-010, 4201-60-0023, 4201-60-030)
Northwest Territories
- Northwest Territories land use permit
- 11 alphanumeric characters with no special characters. (e.g., MV2012C0025, MV2019X0008, MV2019X0027)
Nunavut
- Nunavut land use permit
- 10 alphanumeric characters with no special characters (e.g., N2005X0013, N2012C0026, N2018X0011)
4.1.3 Geographic Information
When reporting geographic information for a facility, it is important to provide the address and geographical coordinates for the physical facility, and not that of the head office of the company. If access to geographic coordinates is not immediately available, searching for a facility through free mapping services available online can provide a reporter with the specific coordinate information.
4.2 Contact information
For each of the following, the name, position, telephone number and email address must be provided:
- technical contact:
- the person who prepared the report and who will be able to answer any questions pertaining to its contents
- a technical contact must be identified
- all correspondence from Environment and Climate Change Canada regarding the NPRI will be sent to the technical contact if no coordinator (see below) is identified
- public contact:
- the person responsible for answering any questions from the public concerning the report
- this name will appear on the NPRI website as the contact for the facility
- a public contact must be identified
- coordinator (if any):
- the person who is responsible for preparing and submitting NPRI reports for more than one facility for the same company
- the coordinator is responsible for answering any questions concerning all of the NPRI reports they filed
- all NPRI correspondence from Environment and Climate Change Canada will be sent to the coordinator, if one is identified
- certifying official:
- the person who is legally responsible for the contents of the NPRI report
- the certifying official is usually the owner or operator, or a company official authorized to act on their behalf
- a certifying official must be identified
- independent contractor (if any):
- if an independent contractor prepared the report, contact information must be provided, including the name of the contracting company
It is important that contact and ownership information be kept up-to-date using the online reporting system or by contacting Environment and Climate Change Canada, if:
- there is a change in the name, telephone number or email address of the contacts identified for the facility
- there is a change in the owner or operator of a facility
4.3 Substance-specific information
Quantities of NPRI substances that are released, disposed of or transferred for recycling that must be reported are described in sections 5-9 of this Guide. The following sections summarize additional information that must be reported.
4.3.1 Information to be reported for Parts 1-3 substances
Nature of the manufacturing, processing or other use of the substance
Facilities are required to indicate whether a substance was manufactured, processed, or otherwise used, by selecting the nature of such activities from a pick-list in the reporting system:
- manufacture:
- for on-site use/processing
- for sale/distribution
- as a by-product
- as an impurity
- process:
- as a reactant
- as a formulation component
- as an article component
- repackaging only
- as a by-product
- otherwise use:
- as a physical or chemical processing aid
- as a manufacturing aid
- ancillary/other use
- as a by-product
- any other releases or disposals of the substance
Reasons why the substance is disposed of or recycled
Facilities are required to indicate why a substance is disposed of or transferred off-site for recycling by selecting from a pick-list in the reporting system:
- production residues
- off-specification products
- expiration date passed
- contaminated materials
- unusable parts or discards
- pollution abatement residues
- machine or finishing residues
- site remediation
- other
Name and location of receiving water bodies
Facilities are required to provide the name and province or territory of any surface water bodies into which NPRI substances are released by direct discharge, spills or leaks. Reporting facilities can select the name of the water body from a list in the online reporting system.
Name and location of receiving off-site facilities
Where NPRI substances are transferred off-site for disposal, treatment prior to final disposal or recycling, facilities are required to provide the name and location of the receiving off-site facilities. Reporting facilities can select the name of the receiving off-site facility from a list in the online reporting system or create a new entry in the system, if the off-site isn’t listed.
Substance concentration data
The average concentration and method detection limit (MDL) in parts per million (ppm) related to the following must be reported:
- a direct discharge to surface waters, based on source testing or direct monitoring
- the disposal or removal of a substance to tailings management areas
- the disposal or removal of a substance in waste rock
The average annual concentration and method detection limit (MDL) in parts per million (ppm) must be reported. Depending on how the concentration measurement was taken, the units can be converted from a percentage (%), mg/kg (for solids) or mg/L (for liquids) into ppm as follows:
0.0001% = 1 ppm
1.0% = 10,000 ppm
1 mg/kg = 1 ppm
1 mg/L = 1 ppm
The MDL of the method used to determine the average annual concentration and the situation upon which the average concentration is based must also be reported. A number of scenarios are possible with multiple measurements of the concentration of a substance in a given process stream:
- all samples are above the detection limit:
- the average concentration is based on the measured concentrations of the substance
- half or more than half of samples above detection limit:
- the average concentration is based on the measured values and half of the MDL for each measurement that is below the MDL
- less than half of samples above detection limit:
- the average concentration is based on the measured values and half of the MDL for each measurement that is below the MDL
- no samples above detection limit:
- if there is no reason to believe that the substance is present, the concentration of the substance in that process can be assumed to be zero
- no sampling:
- other information is used to estimate (this applies to tailings and waste rock reporting)
- no information available on concentration
An indication of whether the reported quantity (release to water or disposal of tailings or waste rock) was estimated using half the MDL is also required. In addition, if more than one MDL applies, this must also be indicated. In the case of multiple MDLs, additional information can be provided in the comment field.
4.3.2 Information to be reported for all substances
Reasons for changes in reported quantities compared to the previous year
Facilities are required to compare their reported quantities in the current year to the previous year and provide the reason(s) for changes in reported quantities from a pick-list in the reporting system:
- increase in production levels
- decrease in production levels
- changes in estimation methods, including changes in emission factors
- specify in comment field the previous estimation method, the current estimation method, and the reason for changing the method
- pollution prevention activities (provide details in the Pollution prevention section of this report)
- changes in quantity and/or composition of combusted materials or fuels
- changes in process and/or raw/produced/processed materials
- changes in composition of materials released/disposed of/transferred
- nature of activities results in annual variation in releases/disposals/transfers
- describe the activity and how it impacts the reported quantity in the comments field
- Activities/events of a non-annual nature
- e.g. a spill, tailings pond breach, or fire
- describe the activity/events in the comments field
- other (specify in comment field)
- no significant change (i.e. <10% or no change)
- not applicable (first year reporting this substance)
Monthly and quarterly breakdown of releases
For Parts 1-3 substances, facilities are required to report a percentage breakdown by quarter. For Parts 4-5 substances, facilities are required to report a percentage breakdown by month. In both cases, percentages must add up to 100%.
4.4 Additional information for electricity generating units
Facilities in all North American Industry Classification System (NAICS) codes that report releases of mercury or criteria air contaminants to air must assign those releases to each electricity generating unit that meets the following criteria:
- the unit has a nameplate capacity of 25 MW or more
- the unit distributes or sells to the grid 33% or more of its potential electrical output
An electricity generation unit means physically connected equipment that operates together to produce electricity for sale or distribution to the grid by means of thermal energy produced by the combustion of fossil fuels and is stationary when used, and is not in or on a machine that is self-propelled.
Potential electrical output means the quantity of electricity that would be generated by a unit in a calendar year if the unit were to operate at capacity at all times during that calendar year.
The 33% threshold must be assessed on an annual basis. If a unit meets the 33% threshold in a calendar year, but does not meet it in the subsequent year, reporting at the unit level for that unit is still required. This requirement applies for three years. For example, if a unit met the 33% threshold only in 2024, emissions from the unit must be reported separately for 2024, 2025 and 2026 reports, but not from 2027 onwards (unless it were to meet the threshold again in a future year).
Facilities that meet the threshold requirements for unit-level reporting must also provide details about the unit, including:
- unit gross generating capacity
- commissioning year
- technology or fuel type
- whether the unit includes emissions from duct firing or other secondary combustion sources
- air pollutant controls installed and operating on the unit
4.5 Pollution prevention activities
Facilities are required to report:
- whether and why a pollution prevention (P2) plan was prepared in that reporting year
- the name of the P2 notice, jurisdiction, or program for which the P2 plan is required
- information on P2 activities undertaken during the year
- the substances for which the P2 activities were undertaken
Environment and Climate Change Canada analyzes P2 information and publishes a summary of the P2 information submitted by facilities in Pollution Prevention in Practice. The published information is updated on an annual basis.
4.6 Comments
Comment fields are provided on many screens in the online reporting system. Comments can be used to provide additional information, such as details about a facility’s operations, how a substance is used, details of pollution prevention activities, reasons for changes in quantities reported from the previous year, or the methods used to calculate reported quantities.
The information provided in comment fields can help users understand the context around the reported information. Clear and concise comments contribute to the understandability and completeness of the NPRI data set. Explanations of changes or anomalies in submitted data help to prevent unnecessary contact with facilities during the quality control process.
4.7 Other requirements
4.7.1 Electronic statement of certification
A statement of certification must be electronically signed and submitted with the NPRI report using the online reporting system. The certifying official should verify that the information submitted is true, complete and accurate, and acknowledge that the data will be made public. The certifying official is legally responsible for the contents of the NPRI report.
4.7.2 Record keeping
Pursuant to subsection 46(8) of CEPA, the owner/operator of a facility is required to retain copies of all information on which their report is based, including any calculations, measurements and other related data, for three years from the applicable reporting deadline. This information must be kept at the facility or at the principal place of business in Canada of the owner/operator of the facility to which the information relates, for three years.
4.7.3 Other reports
There are several other types of NPRI reports that can be filed using the online reporting system:
- Does Not Meet Criteria (DNMC) report:
- a facility that submitted a report for the previous year, but no longer meets NPRI reporting criteria for the current year, is required to submit a “Does Not Meet Criteria” report by the reporting deadline
- Sale/Close/Purchase report:
- submit a “sale/close/purchase” report when transfers of ownership occur, or if a facility closes during the calendar year
- Update:
- an update to current and previous reports can also be submitted using the online reporting system
4.8 Voluntary reporting
The NPRI also accepts voluntary reporting for NPRI substances when a facility does not meet the reporting requirements. Voluntary reports assist the NPRI in providing a more comprehensive description of releases and transfers of pollutants in Canada. A voluntary report for a release, disposal or transfer of a substance should be specified as such by selecting the appropriate option within the online reporting system.
5.1 Requirements for Part 1 substances
Part 1 of the NPRI substance list contains 373 substances or substance groupings that are divided into three categories: Part 1A, Part 1B and Part 1C. Part 1A and Part 1B reporting requirements share many similarities, with the main difference being that substances listed in Part 1B have lower mass and concentration thresholds compared to those in Part 1A. Part 1C contains PFAS that are listed at a lower mass and concentration threshold than substances listed in Part 1A. The following terms apply to Part 1A, Part 1B, and Part 1C substances.
5.1.1 Manufacture, process, or otherwise use
When reporting for substances listed on Part 1, a facility must first consider the quantity of the substance manufactured, processed or otherwise used at the facility. Below is an overview of activities to consider when calculating the quantity of Part 1 substances manufactured, processed, or otherwise used:
- manufacture:
- for on-site use/processing
- for sale/distribution
- incidentally as a by-product
- as an impurity
- process:
- as a reactant
- as a formulation component
- as an article component
- during repackaging
- as a by-product
- otherwise use:
- as a physical or chemical processing aid
- as a manufacturing aid
- for ancillary/other use
- as a by-product
- any other releases or disposals of the substance
- Manufacture
- To produce, prepare or compound an NPRI substance. It also includes the incidental production of an NPRI substance as a by-product. The production of chlorine dioxide by a chemical plant is an example of manufacturing. The production of hydrochloric acid during the manufacture of chlorofluorocarbons is an example of the incidental manufacture of hydrochloric acid.
- Process
- The preparation of an NPRI substance, after its manufacture, for distribution in commerce. Processing includes the preparation of a substance with or without changes in physical state or chemical form. The term also applies to the processing of a mixture or formulation that contains an NPRI substance as one component, the processing of articles (see Glossary for definition), and the processing of a substance as a by-product. The use of chlorine to manufacture hypochloric acid (not an NPRI substance) is an example of processing of chlorine. The use of toluene and xylene to blend paint solvent mixtures is an example of processing without changes in chemical form.
- Otherwise use (or other use)
-
Any use, disposal or release of an NPRI substance that does not fall under the definitions of manufacture or process. This includes the use of the substance as a chemical processing aid, manufacturing aid or some other ancillary use, and the other use of by-products. For example, the use of trichloroethylene in the maintenance of manufacturing and process equipment is an example of an “other use” of that substance. Certain specified uses of substances are excluded and are listed in Section 3.5.2.
The quantity of a substance that is manufactured, processed, or otherwise used is not reported to the NPRI. Instead, if the manufacture, process, or otherwise use threshold is met, the quantity of the substance released, disposed of, or transferred off-site for recycling is required to be reported, even if the quantity is zero.
5.1.2 By-products
The term “by-product” refers to the quantity of an NPRI Part 1 substance that is incidentally manufactured, processed or otherwise used at the facility at any concentration, and released to the environment or disposed of. The quantity of a substance that is recycled or that remains in the final product is not considered to be a by-product for the purpose of the NPRI threshold calculation.
In general, if a quantity of a substance is intentionally manufactured, processed or otherwise used at a facility, then that quantity of the substance is not a by-product, even if it is unintentionally manufactured, processed or otherwise used at another step in the process.
Overall quantities of by-products can be significant, even though their concentration may be low. Therefore, the quantity of a substance that is a by-product must be included in the calculation of the reporting threshold, regardless of concentration. The by-product requirements only apply to Part 1 substances and are only used for the purpose of determining whether or not the mass threshold for a substance has been met.
Some examples of by-products are:
- hydrogen fluoride is incidentally manufactured and released during aluminum smelting
- therefore, the hydrogen fluoride is a by-product and must be included in the calculation of the reporting threshold, regardless of concentration
- manganese and nickel are incidentally present in coal
- during combustion, a portion of these metals is concentrated in the ash, which is disposed of, and a portion of the metals is released in stack emissions
- the weight of the metal by-products, must be included in the calculation of the reporting threshold, regardless of concentration
An example of when substances are not considered by-products:
- metal cuttings, sent for disposal, contain alloyed chromium and nickel at a concentration of less than 1%
- the chromium and nickel are essential components of the alloy; therefore, they are not incidentally processed and are not considered to be by-products
- the chromium and nickel in the metal cuttings do not need to be included in the calculation of the reporting threshold, because the substances are present at a concentration less than the concentration threshold of 1%
5.2 Reporting for Part 1A substances - Core substances
Part 1A lists 177 substances and groups of substances of concern, most of which have been listed on the NPRI since its inception. These substances are commonly referred to as the “core substances,” and comprise the majority of the NPRI substance list.
In general, any person who owns or operates a contiguous facility or offshore installation must submit an NPRI report for a Part 1A substance if both of the following criteria are met:
- employees work a total of ≥ 20,000 hours, or activities to which the employee threshold does not apply (see section 3.4.3) take place at the facility
- the total quantity of the Part 1A substance present in the following scenarios is ≥ 10 tonnes:
- manufactured, processed or otherwise used at a concentration (by weight) of 1% or more
- incidentally manufactured, processed or otherwise used as a by-product at any concentration
- contained in tailings disposed of during the calendar year at any concentration
- contained in waste rock disposed of during the calendar year that is not clean or inert (see section 3.5.4) at a concentration (by weight) of 1% or more
Flow for reporting Part 1A substances
Step 1: Confirm if any of these statements apply:
- the facility is a pipeline installation or portable facility
- the owner/operator is exempt from reporting Part 1A substances (see section 3.5.3)
- employees did not work a total of ≥ 20,000 hours during the calendar year or did activities to which the employee threshold does not apply take place at the facility (see section 3.4.3)
Yes: You are not required to report Part 1A.
No: Continue to Step 2.
Step 2: Add up the following quantities of each Part 1A substance and confirm if you have met the reporting threshold (10 tonnes MPO):
- quantities manufactured, processed, or otherwise used at a concentration ≥ 1%
- quantities incidentally manufactured, processed, or otherwise used as a by-product at any concentration
- quantities contained in tailings at any concentration
- quantities contained in waste rock that is not clean or inert at a concentration ≥ 1%
No (<10 tonnes): The owner/operator is not required to report this substance to Part 1A.
Yes (≥ 10 tonnes): Continue to Step 3.
Step 3: Calculate and report releases, disposals, and transfers for recycling of the Part 1A substance in tonnes. Do not report the threshold amount.
5.2.1 Part 1A substance qualifiers
Some Part 1A substances and groups of substances have additional qualifiers that specify the physical or chemical form, state or particle size of the substance that is to be included. The qualifiers, described below, help to determine whether a report will be required for a given substance.
- "all isomers"
-
Include the total of all isomers reported as an aggregate of the individual isomers.
This qualifier applies to substances:
- cresol (CAS RN 1319-77-3)
- HCFC-122 (41834-16-6)
- HCFC-123 (34077-87-7)
- HCFC-124 (63938-10-3)
- xylene (1330-20-7)
- "and its compounds"
-
Pure chromium and chromium contained in any compound, alloy or mixture must be reported as the equivalent weight of chromium, excluding hexavalent chromium and its compounds.
Pure vanadium and vanadium in any compound or mixture must be reported as the equivalent weight of vanadium. Do not include vanadium contained in an alloy.
For the following substances, the pure metal and the equivalent weight of the metal in any compound, alloy or mixture must be reported as the equivalent weight of the metal itself:
- antimony
- copper
- manganese
- nickel
- zinc
- "and its (their) salts"
-
Weak acids and bases are listed with this qualifier. Although the CAS RN that appears on the NPRI list is specific to the acid or base, all salts of these substances must be reported as an equivalent weight of the acid or base:
- acrylic acid (79-10-7)
- aniline (62-53-3)
- chloroacetic acid (79-11-8)
- cresol (1319-77-3)
- 2,4-diaminotoluene (95-80-7)
- 2,4-dichlorophenol (120-83-2)
- diethanolamine (111-42-2)
- N,N-dimethylaniline (121-69-7)
- 4,6-dinitro-o-cresol (534-52-1)
- hydroquinone (123-31-9)
- Michler’s ketone (90-94-8)
- naphthenic acid fraction compounds (no specific CAS RN applies)
- nitrilotriacetic acid (139-13-9)
- peracetic acid (79-21-0)
- phenol (108-95-2)
- p-phenylenediamine (106-50-3)
- pyridine (110-86-1)
- "expressed as hydrogen sulphide"
-
This qualifier applies for total reduced sulphur (TRS).
Include the total of the following substances expressed as hydrogen sulphide:
- hydrogen sulphide (7783-06-4)
- carbon disulphide (75-15-0)
- carbonyl sulphide (463-58-1)
- dimethyl sulphide (75-18-3)
- methyl mercaptan (74-93-1)
- dimethyl disulphide (624-92-0)
Only releases to air of total reduced sulphur are required to be reported. Quantities of total reduced sulphur released to water, released to land, disposed of and transferred off-site for recycling do not have to be reported.
- "fibrous forms only"
-
This qualifier applies for aluminum oxide (1344-28-1).
Fibrous refers to a synthetic form of aluminum oxide that is processed to produce strands or filaments. This includes the form of aluminum oxide found in brake linings, but excludes the more common granular, powdered or fumed forms of alumina.
- "friable form only"
-
This qualifier applies for asbestos (1332-21-4).
Only asbestos that is brittle and readily crumbled (i.e., friable) should be reported.
- "fume or dust only"
-
This qualifier applies for aluminum (7429-90-5).
Include dry forms of aluminum only, with particle diameters of 0.001-1 micrometre for fumes and 1-100 micrometres for dust. Dust refers to solid particles generated by any mechanical processing of materials including:
- crushing
- grinding
- rapid impact
- handling
- detonation
- decrepitation of organic and inorganic materials such as:
- rock
- ore
- metal
Dusts do not tend to flocculate except under electrostatic forces. A fume is an airborne dispersion consisting of small solid particles created by condensation from the gaseous state, in distinction to a gas or vapor. Fumes arise from the heating of solids. The condensation is often accompanied by a chemical reaction, such as oxidation. Fumes flocculate and sometimes coalesce.
- "in a solution at a pH of 6.0 or more"
-
This qualifier applies for nitrate ion.
This distinguishes nitrate ion in neutral or basic solution from nitric acid (pH of less than 6.0). If nitric acid is neutralized to a pH of 6.0 or greater, report for both nitric acid (7697-37-2) and nitrate ion in solution.
- "ionic"
-
This qualifier applies for cyanides
Includes the salts of hydrogen cyanide, but excludes organocyanides, nitriles and organometallic cyanide compounds.
- "total"
-
This qualifier applies for ammonia and phosphorus.
Include the total of ammonia (NH3) (7664-41-7) and the ammonium ion (NH4+) (14798-03-9) in solution, expressed as ammonia.
Include the total of all phosphorus, not including yellow or white phosphorus (7723-14-0).
- "yellow or white only"
-
This qualifier applies for phosphorus.
Include the total of the yellow and white allotropes of elemental phosphorus only.
5.2.2 Calculating the manufacture, process or otherwise use quantity for Part 1A substances
To calculate the amount to compare to the 10-tonne reporting threshold, add up the following quantities of a Part 1A substance:
- quantities that are manufactured, processed or otherwise used at a concentration equal to or greater than 1% by weight
- quantities that are incidentally manufactured, processed or otherwise used (a by-product), at any concentration, and released on-site to the environment or disposed of on- or off-site
- quantities that are contained in tailings disposed of during the calendar year, at any concentration
- quantities that are contained in waste rock that is not inert and that is disposed of during the calendar year at a concentration equal to or greater than 1% by weight
Any release or disposal of an NPRI substance must be included in the otherwise used category. For example, the quantity of the NPRI substance contained in dust released to air from materials stored on site would be included, whether or not the material is used for a specific purpose at the facility. Another example is a spill of an NPRI substance to water or land during storage or handling.
Since a substance may undergo many processes in a facility, care should be taken not to double-count process streams when calculating the reporting threshold. Do not include quantities of substances more than once in manufacture, process or otherwise use calculations. For example, if a substance is processed and released, the release quantity does not need to be added to the process quantity.
Do not include quantities of a Part 1A substance contained in any of the sources that are excluded, as listed in section 3.5.2, or from the activities listed in section 3.5.3.
A quantity of a substance that is transferred off-site for recycling and returned to the facility should be treated as the equivalent of newly purchased material. A quantity of a substance that is recycled on-site and re-introduced to a process stream (e.g., substances in ore processing water that are recycled back into the process from tailings) should be included in the threshold calculation only once.
The total quantity of a Part 1A substance manufactured, processed or otherwise used at concentrations greater than or equal to 1%, at any time or in any part of the facility, must be included when calculating the 10 tonnes reporting threshold. For example, the quantity of a substance received by a facility at 30% concentration and then diluted to less than 1% for use is included in the threshold calculation. A substance received at the facility at less than 1% and subsequently concentrated to 5% would also be included in the threshold calculation. Activities to consider in the manufacture, process or otherwise use of a substance are listed in section 5.1.
Facilities that repackage or transfer Part 1A substances between containers must consider the entire quantity of the substance contained in the original container or in bulk for threshold calculations.
If only a range of concentrations is available for a substance present in a mixture, contact the supplier of the substance for more detailed information. If no additional information is available, use the average of the range for threshold determinations.
5.2.3 Calculating releases, disposals and transfers for recycling of Part 1A substances
If the reporting threshold for a Part 1A substance is met, a subsequent calculation is required to determine the quantities of that substance that are released, disposed of and transferred for recycling. If the reporting threshold is met, all releases, disposals and transfers for recycling of that substance must be reported, regardless of their concentration or quantity and regardless of whether or not the quantity is used in the threshold calculation. The only exceptions to this are quantities of the substance:
- contained in the materials listed in section 3.5.2
- that are manufactured processed or otherwise used in the activities listed in section 3.5.3
- contained in waste rock where the substance is at a concentration of less than 1% (see section 3.5.4)
5.2.4 Reporting releases, disposals and transfers for recycling of Part 1A substances
All releases, disposals and transfers for recycling of Part 1A substances must be reported in tonnes. Note that the quantity manufactured, processed or otherwise used is not reported.
Note that even if on-site releases, disposals or off-site transfers for recycling are zero or below the mass or concentration thresholds, a report must be submitted for a Part 1A substance, once the 10 tonnes reporting threshold has been met.
When total releases of a Part 1A substance are less than one tonne, a facility may choose to report the release as a total without specifying the environmental media (air, water, or land). Facilities are encouraged to report the breakdown by media, if the information is available.
5.3 Reporting for Part 1B substances – Alternate threshold substances
Part 1B substances may have significant environmental and human health impacts at relatively low levels. Because minimal releases of Part 1B substances may result in significant adverse effects, the reporting thresholds for Part 1B substances are lower than those for Part 1A substances. As such, these substances are commonly referred to as the “alternate threshold substances.”
In general, any person who owns or operates a contiguous facility or an offshore installation must submit a report for a Part 1B substance if both of the following criteria are met:
- employees work a total of ≥ 20,000 hours, or activities to which the employee threshold does not apply (see section 3.4.3) take place at the facility
- the total quantity of the Part 1B substance present in one or more of the following scenarios is greater than or equal to the mass threshold specified in Table 2:
- manufactured, processed or otherwise used at or above the concentration specified in Table 2
- incidentally manufactured, processed or otherwise used as a by-product at any concentration
- contained in tailings at any concentration
- contained in waste rock that is not inert and that is disposed of, at any concentration (see section 3.5.4)
In addition, a facility that is subject to the Chromium Electroplating, Chromium Anodizing and Reverse Etching Regulations must report for hexavalent chromium (and its compounds), regardless of the number of employees and regardless of the mass and concentration thresholds listed in Table 2. If the facility does not meet any other NPRI requirements, only a report for releases, disposals, or transfers of hexavalent chromium (and its compounds) is required.
Flow for reporting Part 1B substances
Step 1: Confirm if the owner/operator subject to the Chromium Electroplating, Chromium Anodizing and Reverse Etching Regulations.
Yes: The owner/operator is required to submit a report for hexavalent chromium compounds. The owner/operator should continue to determine if other Part 1B substances are required to be reported.
No: Continue to Step 2.
Step 2: Confirm if any of these statements apply:
- the facility is a pipeline installation or portable facility
- the owner/operator is exempt from reporting Part 1B substances (see section 3.5.3)
- employees did not work a total of ≥ 20,000 hours during the calendar year or did activities to which the employee threshold does not apply take place at the facility (see section 3.4.3)
Yes: You are not required to report Part 1B.
No: Continue to Step 3.
Step 3: Add up the following quantities of each Part 1B substance and confirm if you have met the reporting threshold (See Table 2):
- quantities manufactured, processed, or otherwise used at a concentration greater than or equal to the concentration threshold (see Table 2)
- quantities incidentally manufactured, processed, or otherwise used as a by-product at any concentration
- quantities contained in tailings at any concentration
- quantities contained in waste rock that is not clean or inert at any concentration
No: The owner/operator is not required to report this substance to Part 1B.
Yes: Continue to Step 4.
Step 4: Calculate and report releases, disposals, and transfers for recycling of the Part 1B substance in kilograms. Do not report the threshold amount.
For Mercury releases, If the facility contained one or more electricity generation units with:
- a capacity of ≥ 25 MW that distributes electricity to the grid
- is ≥ 33% of its electrical output
The owner/operator is required to report mercury releases to air for individual electricity generation units.
| Substance name | Mass reporting threshold (kg) | Concentration by weight |
|---|---|---|
| Acrylonitrile | 1,000 | 0.10% |
| Arsenic (and its compounds) | 50 | 0.10% |
| Azo disperse dyes | 10 | 0.10% |
| Basic Blue 7 | 100 | 1% |
| Basic Violet 3 | 100 | 1% |
| Basic Violet 4 | 100 | 1% |
| 1,4-Benzenediamine, N,N′-mixed phenyl and tolyl derivatives | 50 | 1% |
| Benzothiazoles that can form 2-mercaptobenzothiazole | 100 | 0.10% |
| Bisphenol A | 100 | 1% |
| Cadmium (and its compounds) | 5 | 0.10% |
| Chlorhexidine (and its salts) | 100 | 1% |
| Chlorinated alkanes, medium-chain, CnHxCl(2n+2–x), 14 ≤ n ≤ 17 | 1,000 | 1% |
| Chlorinated alkanes, long-chain, CnHxCl(2n+2–x), 18 ≤ n ≤ 20 | 1,000 | 1% |
| Cobalt (and its compounds) | 50 | 0.10% |
| Ethylene oxide | 1 | 0.10% |
| Free cyanide, cyanide salts, and cyanide complexes | 1,000 | 0.10% |
| Hexavalent chromium (and its compounds)Footnote 3 | 50 | 0.10% |
| Hydrazine (and its salts) | 1,000 | 1% |
| Hydrogen cyanide | 1,000 | 0.10% |
| Isoprene | 100 | 1% |
| Lead (and its compounds) | 50 | 0.10% |
| Long-chain aliphatic amines | 5,000 | 0.10% |
| Malachite Green | 100 | 1% |
| MAPBAP Acetate | 100 | 1% |
| Mercury (and its compounds) | 5 | N/A |
| Nonylphenol and its ethoxylates | 1,000 | 1% |
| 2-Propanone, reaction products with diphenylamine | 50 | 1% |
| Selenium (and its compounds) | 100 | 0.000005% |
| Tetraethyl lead | 50 | 0.10% |
| Thallium (and its compounds) | 100 | 1% |
| Toluene-2,4-diisocyanate | 100 | 0.10% |
| Toluene-2,6-diisocyanate | 100 | 0.10% |
| Toluenediisocyanate (mixed isomers) | 100 | 0.10% |
5.3.1 Part 1B substance qualifiers
Mercury, cadmium, arsenic, hexavalent chromium, lead, cobalt, selenium and thallium are listed with the qualifier “and its compounds.” The pure element and any compound, alloy or mixture of any Part 1B substance must be reported as the equivalent weight of the metal itself. For example, if potassium dichromate (K2Cr2O7, molecular weight = 294 grams per mole [g/mol]) is used, only the mass contribution of hexavalent chromium (2×52 g/mol) in K2Cr2O7 should be included in the threshold calculation for hexavalent chromium.
Note that lead has an additional qualifier: the lead contribution from tetraethyl lead, stainless steel, brass and bronze alloys should be excluded from threshold calculations for lead. Tetraethyl lead should be treated as a separate substance. If the criteria are met, separate reports should be submitted for lead (and its compounds) and tetraethyl lead, with the reporting criteria applied to each substance separately.
Hydrazine and chlorhexidine are listed with the qualifier “and its salts.” Weak acids and bases are listed with this qualifier. Although the CAS RN that appears on the NPRI list is specific to the acid or base, all salts of these substances must be reported as an equivalent weight of the acid or base.
Toluenediisocyanate is listed with the qualifier “mixed isomers.” The total of all isomers occurring in mixtures must be reported.
Any substance whose molecular formula meets the category definition for medium-chain (C14-17) or long- chain (C18-20) chlorinated alkanes must be included when calculating the manufacture, process or otherwise use threshold quantity, and reported if the threshold is exceeded. In addition, chemical mixtures that contain substances that meet the medium-chain (C14-17) or long-chain (C18-20) chlorinated alkane category definition must also be considered. However, for mixtures, NPRI reporting facilities would only include the chlorinated alkane component of the chemical mixture that meets the respective category definition in threshold calculations and reported quantities.
5.3.2 Calculating the manufacture, process or otherwise use quantity for Part 1B substances
To calculate the amount to compare to the reporting threshold, add up the following quantities of a Part 1B substance:
- quantities that are manufactured, processed or otherwise used at a concentration equal to or greater than the concentration threshold (if any) specified in Table 2
- quantities that are incidentally manufactured, processed or otherwise used (a by-product), at any concentration, and released on-site to the environment or disposed of on- or off-site
- quantities that are contained in tailings disposed of during the calendar year, at any concentration
- quantities that are contained in waste rock that is not inert and that is disposed of during the calendar year, at any concentration
Any release or disposal of an NPRI substance must be included in the quantity otherwise used. For example, the quantity of the NPRI substance contained in dust released to air from materials stored on site would be included, whether or not the material is used for a specific purpose at the facility. Another example is a spill of an NPRI substance to water or land during storage or handling.
Since a substance may undergo many processes in a facility, care should be taken not to double-count process streams when calculating the reporting threshold. Do not include quantities of substances more than once in manufacture, process or otherwise use calculations. For example, if a substance is processed and released, the release quantity does not need to be added to the process quantity.
Do not include quantities of a Part 1B substance contained in any of the sources that are excluded, as listed in section 3.5.2, or from the activities listed in section 3.5.3.
As noted previously, quantities of substances disposed of in inert or clean waste rock do not need to be included in threshold calculations. However, the quantity of arsenic contained in inert or clean waste rock can be excluded only if the concentration of arsenic is < 12 mg/kg of waste rock.
5.3.3 Calculating releases, disposals and transfers for recycling of Part 1B substances
If the reporting threshold for a Part 1B substance is met (as discussed in section 5.3.2), a subsequent calculation is required to determine the quantities of that substance that are released, disposed of and transferred for recycling.
If the reporting threshold for a Part 1B substance is met, a subsequent calculation is required to determine the quantities of that substance that are released, disposed of and transferred for recycling. If the reporting threshold is met, all releases, disposals and transfers for recycling of that substance must be reported, regardless of their concentration or quantity and regardless of whether or not the quantity is used in the threshold calculation. The only exceptions to this are quantities of the substance:
- contained in the materials listed in section 3.5.2
- that are manufactured processed or otherwise used in the activities listed in section 3.5.3
5.3.4 Reporting releases, disposals and transfers for recycling of Part 1B substances
All releases, disposals and transfers for recycling of Part 1B substances must be reported in kilograms (kg). Note that the quantity manufactured, processed or otherwise used is not reported.
Any facility that is subject to the Chromium Electroplating, Chromium Anodizing and Reverse Etching Regulations must report releases, disposals, and transfers for recycling of hexavalent chromium (and its compounds), regardless of the number of employees and regardless of the 50 kg mass threshold and 0.1% concentration threshold. If the facility does not meet any other NPRI requirements, only a report for releases, disposals, or transfers of hexavalent chromium (and its compounds) is required.
Note that even if on-site releases, disposals or off-site transfers for recycling are zero or below the mass or concentration thresholds, a report must be submitted for a Part 1B substance once the mass reporting threshold has been met.
5.4 Reporting for Part 1C substances – Per- and polyfluoroalkyl substances (PFAS)
Per- and polyfluoroalkyl substances (PFAS) are a class of thousands of human-made substances. Some typical uses of PFAS include surfactants, lubricants, and repellents (for dirt, water, and grease). PFAS can be found in certain firefighting foams, food packaging, drugs, cosmetics, sunscreens, pesticides, textiles (e.g., carpets, furniture, and clothing), non-stick cookware, vehicles, and electronics. Of the thousands of PFAS, 163 individual PFAS substances are listed on the NPRI (see Table 3), and the reporting thresholds apply to each substance individually.
In general, any person who owns or operates a contiguous facility or an offshore installation must submit a report for a Part 1C substance if both of the following criteria are met:
- employees work a total of ≥ 20,000 hours, or activities to which the employee threshold does not apply (see section 3.4.3) take place at the facility
- the total quantity of the Part 1C substance present in one or more of the following scenarios is greater than or equal to 1 kg:
- manufactured, processed or otherwise used at or above 0.1% concentration;
- incidentally manufactured, processed or otherwise used as a by-product at any concentration;
- contained in tailings at any concentration; and
- contained in waste rock that is not inert and that is disposed of, at any concentration (see section 3.5.4)
Detailed guidance for reporting Part 1C substances can be found in the PFAS Guidance for Reporting to the National Pollutant Release Inventory prepared by Environment and Climate Change Canada.
Flow for reporting Part 1C substances
Step 1: Confirm if any of these statements apply:
- the facility is a pipeline installation or portable facility
- the owner/operator is exempt from reporting Part 1C substances (see section 3.5.3)
- employees did not work a total of ≥ 20,000 hours during the calendar year or did activities to which the employee threshold does not apply take place at the facility (see section 3.4.3)
Yes: You are not required to report Part 1C.
No: Continue to Step 2.
Step 2: Add up the following quantities of each Part 1C substance and confirm if you have met the reporting threshold (1kg):
- quantities manufactured, processed, or otherwise used at a concentration ≥ 0.1%
- quantities incidentally manufactured, processed, or otherwise used as a by-product at any concentration
- quantities contained in tailings at any concentration
- quantities contained in waste rock that is not clean or inert and that is disposed of during the calendar year at any concentration
No: The owner/operator is not required to report this substance to Part 1C.
Yes: Continue to Step 3.
Step 3: Calculate and report releases, disposals, and transfers for recycling of the Part 1C substance in kilograms. Do not report the threshold amount.
| CAS RN | Substance name |
|---|---|
| 1078715-61-3 | 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-[2-[(γ-ω-perfluoro-C4-20-alkyl)thio]acetyl] derivs., inner salts |
| 108427-53-8 | Perfluorohexanesulfonate |
| 113507-82-7 | Perfluoro-2-ethoxyethanesulfonic acid |
| 1169706-83-5 | 3:3 Fluorotelomer carboxylate, ion(1-) |
| 122499-17-6 | Perfluoro-2-propoxypropanoate |
| 126105-34-8 | Perfluorodecanesulfonate |
| 13252-13-6 | Perfluoro-2-propoxypropanoic acid |
| 142636-88-2 | 2-Propenoic acid, 2-methyl-, octadecyl ester, polymer with 3,3,4,4,5,5,6,6,7,7, 8,8,9,9,10,10,11,11,12,12,12heneicosafluorododecyl 2-propenoate, 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10heptadecafluorodecyl 2-propenoate and 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11, 12,12,13,13,14,14,14pentacosafluorotetradecyl 2-propenoate |
| 1432017-36-1 | Perfluoro-4-methoxybutanoate |
| 143372-54-7 | Siloxanes and Silicones, (3,3,4,4,5,5, 6,6,7,7,8,8,9,9,10,10,10heptadecafluorodecyl)oxy Me, hydroxy Me, Me octyl, ethers with polyethylene glycol mono-Me ether |
| 146689-46-5 | Perfluoroheptanesulfonate |
| 149724-40-3 | 8:2 Fluorotelomer sulfonate, ammonium salt |
| 151772-58-6 | Perfluoro-3,6-dioxaheptanoic acid |
| 1621485-21-9 | Perfluoro(2-((6-chlorohexyl)oxy)ethanesulfonate) |
| 16517-11-6 | Octadecanoic acid, pentatriacontafluoro- |
| 1652-63-7 | 1-Propanaminium, 3-[[(heptadecafluorooctyl)sulfonyl]amino]-N,N,N-trimethyl-, iodide |
| 165457-57-8 | Methyl perfluorohexadecanoate |
| 1691-99-2 | 1-Octanesulfonamide, N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-N-(2-hydroxyethyl) |
| 171978-95-3 | Perfluorododecanoate |
| 175905-36-9 | Perfluoropentanesulfonate |
| 1763-23-1 | Perfluorooctane sulfonic acid |
| 17741-60-5 | 2-Propenoic acid, 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12, 12-heneicosafluorododecyl ester |
| 1799325-94-2 | 2H,2H,3H,3H-Perfluorooctanoate |
| 1799325-95-3 | 7:3 Perfluorodecanoate |
| 19430-93-4 | 1-Hexene, 3,3,4,4,5,5,6,6,6-nonafluoro |
| 196859-54-8 | Perfluoroundecanoate |
| 20109-59-5 | Sodium perfluoroheptanoate |
| 2043-53-0 | Decane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8 -heptadecafluoro-10-iodo- |
| 2058-94-8 | Perfluoroundecanoic acid |
| 21049-36-5 | Heptanoic acid, tridecafluoro-, potassium salt |
| 2127366-90-7 | 2,2,3-Trifluoro-3-[1,1,2,2,3,3hexafluoro-3-(trifluoromethoxy) propoxy]propanoate |
| 21615-47-4 | Hexanoic acid, undecafluoro-, ammonium salt |
| 21652-58-4 | Perfluorooctyl ethylene |
| 21934-50-9 | Perfluoroheptanesulfonic acid, sodium salt |
| 2196242-82-5 | 2-[(8-Chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7, 8,8-hexadecafluorooctyl)oxy]-1,1,2,2-tetrafluoroethanesulfonate |
| 220689-13-4 | Perfluoro-2-ethoxyethanesulfonate |
| 2218-54-4 | Butanoic acid, 2,2,3,3,4,4,4-heptafluoro-, sodium salt (1:1) |
| 2250081-67-3 | Sodium 4,8-dioxa-3Hperfluorononanoate |
| 2263-09-4 | 1-Octanesulfonamide, N-butyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-N-(2-hydroxyethyl)- |
| 2355-31-9 | 2-(N-Methylperfluorooctanesulfonamido)acetic acid |
| 24448-09-7 | 1-Octanesulfonamide, 1,1,2,2,3,3,4,4,5,5, 6,6,7,7,8,8,8-heptadecafluoro-N-(2-hydroxyethyl)-N-methyl- |
| 25268-77-3 | 2-[[(Heptadecafluorooctyl)sulfonyl]methylamino]ethyl acrylate |
| 2706-90-3 | Perfluoropentanoic acid |
| 2706-91-4 | Perfluoropentanesulfonic acid |
| 27619-96-1 | 8:2 Fluorotelomer sulfonate, sodium salt |
| 27619-97-2 | 1-Octanesulfonic acid, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro |
| 27854-31-5 | 2-(Perfluorooctyl)ethanoic acid |
| 27905-45-9 | 2-Propenoic acid, 3,3,4,4,5,5,6,6,7,7,8,8, 9,9,10,10,10-heptadecafluorodecyl ester |
| 2795-39-3 | Perfluorooctane sulfonic acid, potassium salt |
| 2806-15-7 | Sodium perfluorodecanesulfonate |
| 29081-56-9 | Perfluorooctane sulfonic acid, ammonium salt |
| 29117-08-6 | Poly(oxy-1,2-ethanediyl), α-[2-[ethyl[(heptadecafluorooctyl)sulfonyl]amino]ethyl]-ω-hydroxy- |
| 2923-16-2 | Trifluoroacetate salt of potassium |
| 2923-18-4 | Trifluoroacetic acid, sodium salt |
| 2966-50-9 | Trifluoroacetic acid, silver salt |
| 2991-50-6 | 2-(N-Ethylperfluorooctanesulfonamido)acetic acid |
| 30334-69-1 | Perfluorobutanesulfonamide |
| 307-24-4 | Perfluorohexanoic acid |
| 307-35-7 | Perfluorooctylsulfonyl fluoride |
| 307-55-1 | Perfluorododecanoic acid |
| 307-67-5 | Perfluorododecanoic acid, sodium salt |
| 31506-32-8 | 1-Octanesulfonamide, 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8heptadecafluoro-N-methyl- |
| 3336-58-1 | Trifluoroacetic acid, ammonium salt |
| 335-66-0 | Octanoyl fluoride, pentadecafluoro- |
| 335-67-1 | Perfluorooctanoic acid |
| 335-76-2 | Perfluorodecanoic acid |
| 335-77-3 | Perfluorodecanesulfonic acid |
| 335-95-5 | Perfluorooctanoic acid, sodium salt |
| 34362-49-7 | 1,1,2,2-Tetrahydroperfluorohexadecyl acrylate |
| 343629-43-6 | Perfluorododecanesulfonate |
| 34395-24-9 | 2-Propenoic acid, 3,3,4,4,5,5,6,6,7,7,8,8, 9,9,10,10,11,11,12,12,13,13,14,14, 14-pentacosafluorotetradecyl ester |
| 355-46-4 | Perfluorohexanesulfonic acid |
| 356-02-5 | 3:3 Fluorotelomer carboxylic acid |
| 365971-87-5 | Perfluorotetradecanoate |
| 37338-48-0 | Poly[oxy(methyl-1,2-ethanediyl)], α-[2-[ethyl[(heptadecafluorooctyl)sulfonyl]amino]ethyl]-ω-hydroxy- |
| 375-22-4 | Perfluorobutanoic acid |
| 375-73-5 | Perfluorobutanesulfonic acid |
| 375-85-9 | Perfluoroheptanoic acid |
| 375-92-8 | Perfluoroheptanesulfonic acid |
| 375-95-1 | Perfluorononanoic acid |
| 376-06-7 | Perfluorotetradecanoic acid |
| 376-27-2 | Methyl perfluorooctanoate |
| 377-73-1 | Perfluoro-3-methoxypropanoic acid |
| 382-21-8 | Perfluoroisobutene |
| 3830-45-3 | Perfluorodecanoic acid, sodium salt |
| 38436-16-7 | Dichloromethyl(3,3,4,4,5,5,6,6,6nonafluorohexyl)silane |
| 3871-99-6 | Perfluorohexanesulfonic acid, potassium salt |
| 39108-34-4 | 8:2 Fluorotelomer sulfonic acid |
| 39187-41-2 | Methyl perfluoro-3,6-dioxaheptanoate |
| 414911-30-1 | 4:2 Fluorotelomer sulfonate |
| 4151-50-2 | 1-Octanesulfonamide, N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro |
| 425670-75-3 | 3,3,4,4,5,5,6,6,7,7,8,8,8Tridecafluorooctane-1-sulfonate |
| 45048-62-2 | Perfluorobutanoate |
| 45167-47-3 | Perfluoropentanoate |
| 45187-15-3 | Perfluorobutanesulfonate |
| 45285-51-6 | Perfluorooctanoate |
| 45298-90-6 | Perfluorooctanesulfonate |
| 474511-07-4 | Perfluorononanesulfonate |
| 481071-78-7 | 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10Heptadecafluorodecane-1-sulfonate |
| 507-63-1 | Perfluorooctyl iodide |
| 53826-12-3 | 2-(Perfluorohexyl)ethanoic acid |
| 56773-42-3 | Ethanaminium, N,N,N-triethyl-, salt with 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8heptadecafluoro-1-octanesulfonic acid (1:1) |
| 59587-39-2 | 1-Octanesulfonic acid, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-, ammonium salt |
| 60871-96-7 | Sodium perfluoro-n-undecanoate |
| 6130-43-4 | Heptanoic acid, tridecafluoro-, ammonium salt |
| 62037-80-3 | Hexafluoropropylene oxide dimer acid, ammonium salt |
| 647-42-7 | 1-Octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro- |
| 65104-45-2 | 2-Propenoic acid, 2-methyl-, 3,3,4,4,5,5, 6,6,7,7,8,8,9,9,10,10,11,11,12,12,12heneicosafluorododecyl ester, polymer with 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10, 10-heptadecafluorodecyl 2-methyl2-propenoate, methyl 2-methyl2-propenoate, and 3,3,4,4,5,5,6,6,7,7,8,8tridecafluorooctyl 2-methyl-2-propenoate |
| 65530-61-2 | Poly(difluoromethylene), α-fluoro-ω-[2-(phosphonooxy)ethyl]- |
| 65530-62-3 | Poly(difluoromethylene), α,α′-[phosphinicobis(oxy-2,1-ethanediyl)]bis[ω-fluoro |
| 65530-63-4 | Ethanol, 2,2′-iminobis-, compd. with α-fluoro-ω-[2-(phosphonooxy)ethyl] poly(difluoromethylene) (2:1) |
| 65530-64-5 | Ethanol, 2,2′-iminobis-, compd. with α,α′-[phosphinicobis(oxy-2,1-ethanediyl)] bis[ω-fluoropoly(difluoromethylene)] (1:1) |
| 65530-69-0 | Poly(difluoromethylene), α-[2-[(2-carboxyethyl)thio]ethyl]-ω-fluoro-, lithium salt (1:1) |
| 65530-70-3 | Poly(difluoromethylene), α,α′-[phosphinicobis(oxy-2,1-ethanediyl)]bis[ω-fluoro-, ammonium salt (1:1) |
| 65530-72-5 | Poly(difluoromethylene), α-fluoro-ω-[2-(phosphonooxy)ethyl]-, ammonium salt (1:2) |
| 65530-83-8 | Poly(difluoromethylene), α-[2-[(2-carboxyethyl)thio]ethyl]-ω-fluoro |
| 65545-80-4 | Poly(oxy-1,2-ethanediyl), α-hydro-ω-hydroxy-, ether with α-fluoro-ω-(2-hydroxyethyl)poly(difluoromethylene) (1:1) |
| 65605-58-5 | 2-Propenoic acid, 2-methyl-, dodecyl ester, polymer with α-fluoro-ω-[2-[(2-methyl-1-oxo-2-propenyl)oxy]ethyl]poly(difluoromethylene) |
| 65605-73-4 | Poly(difluoromethylene), α-fluoro-ω-[2-[(1-oxo-2-propenyl)oxy]ethyl]-, homopolymer |
| 65636-35-3 | Ethanaminium, N,N-diethyl-N-methyl-2[(2-methyl-1-oxo-2-propenyl)oxy]-, methyl sulfate, polymer with 2-ethylhexyl 2-methyl-2-propenoate, α-fluoro-ω-[2-[(2-methyl-1-oxo-2propenyl)oxy]ethyl]poly (difluoromethylene), 2-hydroxyethyl 2-methyl-2-propenoate and N-(hydroxymethyl)-2-propenamide |
| 67584-58-1 | 1-Propanaminium, N,N,N-trimethyl-3-[[(pentadecafluoroheptyl)sulfonyl]amino]-, iodide |
| 678-39-7 | 1-Decanol, 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10, 10,10-heptadecafluoro- |
| 67905-19-5 | Perfluorohexadecanoic acid |
| 68140-18-1 | Thiols, C4-10, γ-ω-perfluoro |
| 68140-20-5 | Thiols, C6-12, γ-ω-perfluoro |
| 68140-21-6 | Thiols, C10-20, γ-ω-perfluoro |
| 68187-47-3 | 1-Propanesulfonic acid, 2-methyl-, 2-[[1-oxo-3-[(γ-ω-perfluoro-C4-16-alkyl)thio]propyl]amino] derivs., sodium salts |
| 68227-96-3 | 2-Propenoic acid, butyl ester, telomer with 2-[[(heptadecafluorooctyl)sulfonyl] methylamino]ethyl 2-propenoate, 2-[methyl[(nonafluorobutyl) sulfonyl]amino]ethyl 2-propenoate, α-(2-methyl-1-oxo-2-propenyl)-ωhydroxypoly(oxy-1,4-butanediyl), α-(2-methyl-1-oxo-2-propen-1-yl)-ω[(2-methyl-1-oxo-2-propen-1-yl)oxy]poly (oxy-1,4-butanediyl), 2-[methyl[ (1,1,2,2,3,3,4,4,5,5,6,6,7,7,7pentadecafluoroheptyl)sulfonyl] amino]ethyl 2-propenoate, 2-[methyl[ (1,1,2,2,3,3,4,4,5,5,6,6,6tridecafluorohexyl)sulfonyl]amino] ethyl 2-propenoate, 2-[methyl[ (1,1,2,2,3,3,4,4,5,5,5-undecafluoropentyl) sulfonyl]amino]ethyl 2-propenoate and 1-octanethiol |
| 68259-10-9 | 1-Butanesulfonic acid, 1,1,2,2,3,3,4,4,4-nonafluoro-, ammonium salt |
| 68259-11-0 | Pentanoic acid, nonafluoro-, ammonium salt |
| 68259-12-1 | Perfluorononanesulfonic acid |
| 68391-08-2 | Alcohols, C8-14, γ-ω-perfluoro |
| 68391-09-3 | Sulfonic acids, C6-12-alkane, perfluoro potassium salts |
| 68412-68-0 | Phosphonic acid, perfluoro-C6-12-alkyl derivs. |
| 68412-69-1 | Phosphinic acid, bis(perfluoro-C6-12-alkyl) derivs. |
| 68957-57-3 | 1-Propanaminium, N,N,N-trimethyl-3-[[(undecafluoropentyl)sulfonyl]amino]-, iodide |
| 68957-58-4 | 1-Propanaminium, N,N,N-trimethyl-3-[[(tridecafluorohexyl)sulfonyl]amino]-, iodide |
| 68958-60-1 | Poly(oxy-1,2-ethanediyl), α-[2-[ethyl[(pentadecafluoroheptyl)sulfonyl]amino]ethyl]-ω-methoxy- |
| 70887-84-2 | 2H-Perfluoro-2-decenoic acid |
| 70887-88-6 | 2H-Perfluoro-2-octenoic acid (6:2) |
| 70969-47-0 | Thiols, C8-20, γ-ω-perfluoro, telomers with acrylamide |
| 70983-60-7 | 1-Propanaminium, 2-hydroxy-N,N,N-trimethyl-, 3-[(γ-ω-perfluoro-C6-20-alkyl)thio] derivs., chlorides |
| 72007-68-2 | Perfluorononanoate |
| 72629-94-8 | Perfluorotridecanoic acid |
| 72654-51-4 | Acetic acid, trifluoro-, rhodium(2+) salt |
| 73829-36-4 | Perfluorodecanoate |
| 754-91-6 | Perfluorooctanesulfonamide |
| 756426-58-1 | Perfluoro(2-((6-chlorohexyl)oxy)ethanesulfonic acid) |
| 757124-72-4 | 2-(Perfluorobutyl)-1-ethanesulfonic acid |
| 76-05-1 | Acetic acid, trifluoro- |
| 763051-92-9 | 11-Chloroperfluoro-3-oxaundecanesulfonic acid |
| 79780-39-5 | Perfluorododecanesulfonic acid |
| 798556-82-8 | Perfluorooctadecanoate anion |
| 812-70-4 | 3-(Perfluoroheptyl)propanoic acid |
| 83329-89-9 | 11-Chloroperfluoro-3-oxaundecanesulfonate, potassium salt |
| 862374-87-6 | Perfluorotridecanoate |
| 863090-89-5 | Perfluoro-4-methoxybutanoic acid |
| 865-86-1 | 1-Dodecanol, 3,3,4,4,5,5,6,6,7,7,8,8,9,9, 10,10,11,11,12,12,12-heneicosafluoro |
| 914637-49-3 | 2H,2H,3H,3H-Perfluorooctanoic acid |
| 919005-14-4 | 4,8-Dioxa-3H-perfluorononanoic acid |
| 92612-52-7 | Perfluorohexanoate |
| 93572-72-6 | Sulfonic acids, C6-12-alkane, perfluoro |
| 98789-57-2 | Perfluorononanesulfonic acid, sodium salt |
5.4.1 Calculating the manufacture, process or otherwise use quantity for Part 1C substances
Facilities need to determine which products they MPO contain any of the 163 PFAS listed in the NPRI. Sources of information to identify the presence of individual PFAS can involve reviewing the Safety Data Sheet and/or Technical Data Sheet for the products that the facility MPOs that have the potential of containing PFAS. Contacting the manufacturer or supplier of these products could also be a source to obtain relevant information.
To calculate the amount to compare to the reporting threshold, add up the following quantities of each Part 1C substance:
- quantities that are manufactured, processed or otherwise used at a concentration equal to or greater than 0.1%
- quantities that are incidentally manufactured, processed or otherwise used (a by-product), at any concentration, and released on-site to the environment or disposed of on- or off-site
- quantities that are contained in tailings disposed of during the calendar year, at any concentration
- quantities that are contained in waste rock that is not inert and that is disposed of during the calendar year, at any concentration
Any release or disposal of an NPRI substance must be included in the quantity otherwise used. For example, the quantity of the NPRI substance contained in dust released to air from materials stored on site would be included, whether or not the material is used for a specific purpose at the facility. Another example is a spill of an NPRI substance to water or land during storage or handling.
Since a substance may undergo many processes in a facility, care should be taken not to double-count process streams when calculating the reporting threshold. Do not include quantities of substances more than once in manufacture, process or otherwise use calculations. For example, if a substance is processed and released, the release quantity does not need to be added to the process quantity.
Do not include quantities of a Part 1C substance contained in any of the sources that are excluded, as listed in section 3.5.2, or from the activities listed in section 3.5.3.
5.4.2 Calculating releases, disposals and transfers for recycling of Part 1C substances
If the reporting threshold for a Part 1C substance is met (as discussed in section 5.4), a subsequent calculation is required to determine the quantities of that substance that are released, disposed of and transferred for recycling. If the reporting threshold is met, all releases, disposals and transfers for recycling of that substance must be reported, regardless of their concentration or quantity and regardless of whether or not the quantity is used in the threshold calculation. The only exceptions to this are quantities of the substance:
- contained in the materials listed in section 3.5.2
- that are manufactured processed or otherwise used in the activities listed in section 3.5.3
5.4.3 Reporting releases, disposals and transfers for recycling of Part 1C substances
All releases, disposals and transfers for recycling of Part 1C substances must be reported in kilograms (kg). Note that the quantity manufactured, processed or otherwise used is not reported.
Note that even if on-site releases, disposals or off-site transfers for recycling are zero or below the mass or concentration thresholds, a report must be submitted for a Part 1C substance once the mass reporting threshold has been met.
6. Reporting for Part 2 substances – Polycyclic aromatic hydrocarbons
Polycyclic aromatic hydrocarbons (PAHs) may be used as commercial chemicals, incidentally manufactured in certain industrial processes and during combustion, or contained in tailings. There are 31 PAHs listed in Part 2 of the NPRI substance list.
6.1 Reporting criteria for Part 2 substances
With the exception of facilities where wood preservation using creosote takes place (see below), reporting for PAHs is based on the quantities of PAHs that are released, disposed of or transferred for recycling as a result of incidental manufacture or from the generation of tailings. A person who owns or operates a contiguous facility, a portable facility, or an offshore installation must submit reports for PAHs if both of the following criteria are met:
- employees work a total of ≥ 20,000 hours, or activities to which the employee threshold does not apply (listed in section 3.4.3) take place at the facility
- the sum of all PAHs released, disposed of or transferred off-site for recycling as a result of incidental manufacture and/or as a result of the generation of tailings is ≥ 50 kg
Wood preservation facilities using creosote must report for Part 2 substances, regardless of quantities and regardless of the number of hours worked by employees. See the Guidance for wood preservation facilities reporting to the NPRI for more information.
Flow for reporting Part 2 substances
Step 1: Confirm if any of these statements apply:
- the facility is a pipeline installation or portable facility
- the owner/operator is exempt from reporting Part 2 substances (see section 3.5.3)
Yes: You are not required to report Part 2.
No: Continue to Step 2.
Step 2: Confirm if Part 2 substances were released, disposed of or transferred for recycling from a wood preservation process using creosote.
Yes: The owner/operator is required to submit a report for Part 2 substances. Skip to Step 5.
No: Continue to Step 3.
Step 3: Confirm if the employee threshold applies:
- employees did not work a total of ≥ 20,000 hours during the calendar year or did activities to which the employee threshold does not apply take place at the facility (see section 3.4.3)
Yes: You are not required to report Part 2.
No: Continue to Step 4.
Step 4: For all Part 2 substances, add up the quantities released, disposed of, or transferred for recycling:
- as a result of incidental manufacture as a by-product at any concentration
- as a result of the generation of tailings
Confirm if the combined total for all substances is ≥ 50kg.
No: you are not required to report Part 2.
Yes: Continue to Step 5
Step 5: Submit a report for Part 2 substances.
There are three ways to report Part 2 substances, based on available information:
- if information on releases, disposals and transfers for recycling for individual PAHs is available:
- PAHs in quantities ≥ 5 kg must be reported individually
- If only a combination of information on individual and total PAHs is available:
- PAHs in quantities ≥ 5kg and quantities of “total unspeciated PAHs” should both be reported
- If the only available information is for total PAHs:
- “total unspeciated PAHs” should be reported
6.2 Reporting releases, disposals and transfers for recycling of Part 2 substances
All releases, disposals and transfers for recycling of Part 2 substances must be reported in kilograms.
If the 50 kg threshold is met, or if wood preservation using creosote takes place at the facility, a report must be submitted for PAHs. Releases, disposals and transfers for recycling must be reported for the individual PAHs, even though the 50 kg threshold applies to the aggregate total of all 31 PAHs.
Depending on the information that is available, there are three ways to report PAHs:
- if information on releases, disposals and transfers for recycling for quantities of individual PAHs is available:
- add quantities of individual PAHs
- if the total is ≥ 50kg:
- report quantities of individual PAHs that are released, disposed of or transferred for recycling in quantities ≥ 5 kg
- quantities of individual PAHs that are < 5 kg are not required to be reported
- if only a combination of information on the quantities of individual and the quantity total PAHs is available:
- add quantities of total PAHs and any individual PAHs that are not already included in the total unspeciated PAHs
- if the total is ≥ 50kg:
- report quantities of individual PAHs that are ≥ 5 kg, and
- report “total unspeciated PAHs” (not including quantities of individually reported PAHs)
- quantities of individual PAHs that are < 5 kg are not required to be reported
- if the only available information is for the quantity of total PAHs:
- if total PAHs are ≥ 50kg report “total unspeciated PAHs”
Note that “total unspeciated PAHs” is not intended to include the quantity of PAHs that are reported individually. In order to avoid double counting when reporting both individual PAHs and “total unspeciated PAHs”, the quantities of individual PAHs that are reported separately should not be included in the quantity reported for “total unspeciated PAHs”.
In addition, do not include release, disposal and transfer for recycling quantities of PAHs from activities listed in section 3.5.3 when reporting PAHs. Do not include release, disposal and transfer for recycling quantities of naphthalene (PAH listed in Part 1A) when reporting for total PAHs.
Facilities using creosote for wood preservation must report for PAHs regardless of the quantity of PAHs released, disposed of or transferred for recycling or the number of hours worked by employees.
7. Reporting for Part 3 substances – Dioxins, furans and hexachlorobenzene
Polychlorinated dibenzo-p-dioxins (dioxins), polychlorinated dibenzofurans (furans) and hexachlorobenzene are released primarily as by-products of industrial and combustion processes; they are also found as contaminants in certain pesticides or chlorinated solvents. Hexachlorobenzene may also be found as a contaminant in the wood preservative pentachlorophenol (PCP).
Hexachlorobenzene and 17 dioxin and furan congeners are listed in Part 3. For a list of these congeners, see Table 4.
7.1 Reporting criteria for Part 3 substances
Reporting for dioxins, furans and hexachlorobenzene is mandatory for a contiguous facility, a portable facility or an offshore installation where the activities specified below take place, regardless of quantity or concentration. The employee threshold applies to some of these activities, but does not apply to others, as indicated below. For those activities to which the employee threshold applies, both criteria must be met (i.e., the activity must take place, and the employee threshold must be met). For activities to which the employee threshold does not apply, reporting for dioxins, furans and hexachlorobenzene is mandatory, regardless of the number of hours worked by employees.
The employee threshold does not apply to wood preservation activities in general. However, only wood preservation using PCP triggers mandatory reporting of Part 3 substances. PCP, by its chemical structure, is a close surrogate to hexachlorobenzene. PCP is derived from hexachlorobenzene by substituting one of HCB’s six chloro-substituents with a hydroxyl group. Given its chemical similarity to HCB and that its manufacturing ingredients contain the precursors for dioxin and furan production (i.e., chlorinated aromatics), the manufacture of PCP often results in the incidental manufacture of HCB, dioxins and furans.
Activities for which reports on dioxins, furans and hexachlorobenzene are required:
- activities where the employee threshold does not apply:
- non-hazardous solid waste incineration of ≥ 26 tonnes of waste
- including conical burners and beehive burners
- biomedical or hospital waste incineration of ≥ 26 tonnes of waste
- hazardous waste incineration
- sewage sludge incineration
- wood preservation using pentachlorophenol
- non-hazardous solid waste incineration of ≥ 26 tonnes of waste
- activities where the employee threshold applies:
- base metals smelting (copper, lead, nickel or zinc only)
- smelting of secondary aluminum
- smelting of secondary lead
- production of iron ore pellets using an induration furnace or manufacturing of sinter using the iron sintering process
- operation of electric arc furnaces in steel foundries
- operation of electric arc furnaces in steel manufacturing
- production of magnesium
- manufacturing of Portland cement
- production of chlorinated organic solvents or chlorinated monomers
- combustion of fossil fuel in a boiler unit, with a nameplate capacity of ≥ 25 megawatts of electricity, for the purpose of producing steam for the production of electricity
- combustion of hog fuel originating from logs that were transported or stored in salt water in the pulp and paper sector
- combustion of fuel in kraft liquor boilers used in the pulp and paper sector
- titanium dioxide pigment production using the chloride process
Flow for reporting Part 3 substances
Step 1: Confirm if any of the following activities take place at the facility:
- non-hazardous solid waste incineration of ≥ 26 tonnes of waste, including with conical burners and beehive burners
- biomedical or hospital waste incineration of ≥ 26 tonnes of waste
- hazardous waste incineration
- sewage sludge incineration
- wood preservation using pentachlorophenol
Yes: The owner/operator is required to submit a report for Part 3 substances. Skip to Step 4.
No: Continue to Step 2.
Step 2: Confirm if employees work a total of ≥ 20,000 hours during the calendar year.
No: The owner/operator is not required to submit a report for Part 3 substances.
Yes: Continue to Step 3.
Step 3: Confirm if any of the following activities take place at the facility:
- base metals smelting (copper, lead, nickel or zinc only)
- smelting of secondary aluminum
- smelting of secondary lead
- production of iron ore pellets using an induration furnace or manufacturing of sinter using the iron sintering process
- operation of electric arc furnaces in steel foundries
- operation of electric arc furnaces in steel manufacturing
- production of magnesium
- manufacturing of Portland cement
- production of chlorinated organic solvents or chlorinated monomers
- combustion of fossil fuel in a boiler unit, with a nameplate capacity of ≥ 25 megawatts of electricity, for the purpose of producing steam for the production of electricity
- combustion of hog fuel originating from logs that were transported or stored in salt water in the pulp and paper sector
- combustion of fuel in kraft liquor boilers used in the pulp and paper sector
- titanium dioxide pigment production using the chloride process
No: The owner/operator is not required to submit a report for Part 3 substances.
Yes: The owner/operator is required to submit a report for Part 3 substances (from the specified activities only). Continue to Step 4.
Step 4: Report dioxins and furans.
There are two ways to report based on available information:
if information on individual congeners is available, submit reports for the individual congeners in grams
if only total dioxins and furans is available, report the total in grams of toxic equivalents (TEQ)
7.2 Reporting releases, disposals and transfers for recycling of Part 3 substances
Only those quantities of dioxins, furans and hexachlorobenzene that result from the activities listed in section 7.1 need to be reported. Quantities of Part 3 substances that result from other activities do not need to be reported.
The information that needs to be reported for Part 3 substances depends on the method used to determine the quantities released, disposed of and transferred for recycling. There are three possible scenarios:
- quantities are determined using CEMS, PEM or source testing
- quantities are estimated using other methods
- no information is available
To determine what is required to be reported, the quantities determined using CEMS, PEM or source testing must be compared to the level of quantification (LoQ). LoQ is defined in CEPA as “the lowest concentration that can be accurately measured using sensitive but routine sampling and analytical methods.” The estimated LoQs for dioxins, furans and HCB, determined by Environment and Climate Change Canada for gases, liquids and solids are listed below:
- dioxins and furansFootnote 4 :
- gasesFootnote 5 - 32 picograms (pg) toxicity equivalents (TEQ)/m3
- solidFootnote 6 - 9 pg TEQ/g
- liquidFootnote 7 - 20 pg TEQ/L
- hexachlorobenzene:
- gasesFootnote 5 - 6 nanograms (ng)/m3
- solidFootnote 6 - 2 ng/g
- liquidFootnote 7 - 70 ng/L
Measured concentrations must be compared to the LoQ for each type of release, disposal and transfer for recycling. If measured quantities are greater than or equal to the LoQ, the quantities must be reported. If measured quantities are less than the LoQ, reporting the quantities is optional.
If quantities of dioxins, furans and HCB are estimated using remote quantification, mass balance, emission factors, a speciation profile or engineering estimates, the quantities that are released, disposed of or transferred for recycling do not need to be compared to an LoQ, and must be reported.
The online reporting system allows up to six decimal places to be reported. If a quantity is being reported, it must be 0.000001 g or more. Below summarizes the information that should be reported for Part 3 substances depending on the method of estimation:
- CEMS, PEM, or source testing:
- If at or above LoQ report the quantity, and report that the quantity is at or above the LoQ (detail code “AL” in the reporting system)
- If below LoQ report that the quantity is below the LoQ (detail code “BL”)
- the quantity can also be reported, but this is optional when it is below the LoQ (detail code “BQ”)
- remote quantification, mass balance, a site-specific / published emission factor, speciation profile, or an engineering estimate:
- report the quantity
- no quantity was able to be determined, or no information is available:
- report that no information is available under “Basis of Estimate” in the reporting system (detail code “NI”)
7.2.1 Reporting dioxins and furans as individual congeners or toxic equivalents
Depending on the information that is available, there are two ways to report dioxins and furans:
- Information on individual congeners of dioxins and furans must be reported if it is available, in grams
- If the only information available is for total dioxins and furans, the total must be reported in grams of toxic equivalents (TEQ)
Dioxins and furans are often found in complex mixtures, typically at extremely low concentrations, making it difficult to determine the cumulative toxicity of the mixture. Accordingly, toxic equivalency factors (TEFs) have been assigned to each dioxin and furan congener as weighting factors. These TEFs are assigned relative to the toxicity of 2,3,7,8-TCDD, the most toxic congener.
The TEFs listed in Table 4 should be used. To calculate TEQ: multiply the concentration (or quantity) of an individual congener by its respective TEF. For example, 1,2,3,4,7,8-HxCDF has a TEF of 0.1, and a sample concentration of 30 ng/kg 1,2,3,4,7,8-HxCDF is therefore equal to 3 ng TEQ/kg.
| Congener | Abbreviation | CAS RN | Toxicity equivalent factor |
|---|---|---|---|
| 2,3,7,8-Tetrachlorodibenzo-p-dioxin | 2,3,7,8-TCDD | 1746-01-6 | 1 |
| 1,2,3,7,8-Pentachlorodibenzo-p-dioxin | 1,2,3,7,8-PeCDD | 40321-76-4 | 1 |
| 1,2,3,4,7,8-Hexachlorodibenzo-p-dioxin | 1,2,3,4,7,8-HxCDD | 39227-28-6 | 0.1 |
| 1,2,3,6,7,8-Hexachlorodibenzo-p-dioxin | 1,2,3,6,7,8-HxCDD | 57653-85-7 | 0.1 |
| 1,2,3,7,8,9-Hexachlorodibenzo-p-dioxin | 1,2,3,7,8,9-HxCDD | 19408-74-3 | 0.1 |
| 1,2,3,4,6,7,8-Heptachlorodibenzo-p-dioxin | 1,2,3,4,6,7,8-HpCDD | 35822-46-9 | 0.01 |
| Octachlorodibenzo-p-dioxin | OCDD | 3268-87-9 | 0.0003 |
| 2,3,7,8-Tetrachlorodibenzofuran | 2,3,7,8-TCDF | 51207-31-9 | 0.1 |
| 2,3,4,7,8-Pentachlorodibenzofuran | 2,3,4,7,8-PeCDF | 57117-31-4 | 0.3 |
| 1,2,3,7,8-Pentachlorodibenzofuran | 1,2,3,7,8-PeCDF | 57117-41-6 | 0.03 |
| 1,2,3,4,7,8-Hexachlorodibenzofuran | 1,2,3,4,7,8-HxCDF | 70648-26-9 | 0.1 |
| 1,2,3,7,8,9-Hexachlorodibenzofuran | 1,2,3,7,8,9-HxCDF | 72918-21-9 | 0.1 |
| 1,2,3,6,7,8-Hexachlorodibenzofuran | 1,2,3,6,7,8-HxCDF | 57117-44-9 | 0.1 |
| 2,3,4,6,7,8-Hexachlorodibenzofuran | 2,3,4,6,7,8-HxCDF | 60851-34-5 | 0.1 |
| 1,2,3,4,6,7,8-Heptachlorodibenzofuran | 1,2,3,4,6,7,8-HpCDF | 67562-39-4 | 0.01 |
| 1,2,3,4,7,8,9-Heptachlorodibenzofuran | 1,2,3,4,7,8,9-HpCDF | 55673-89-7 | 0.01 |
| Octachlorodibenzofuran | OCDF | 39001-02-0 | 0.0003 |
Source: Van den Berg, Et al. (2006). The 2005 World Health Organization reevaluation of human and Mammalian toxic equivalency factors for dioxins and dioxin-like compounds. Toxicological Sciences, Volume 93, Issue 2, pp. 223-241. https://doi.org/10.1093/toxsci/kfl055.
8. Reporting for Part 4 substances – Criteria air contaminants
Air issues, such as smog and acid rain, result from the presence of, and interactions between, a group of pollutants known as criteria air contaminants (CACs) and related pollutants. There are seven CACs listed in Part 4 (see section 8.5). The following sections provide information on what should be included and excluded when reporting releases of CACs.
8.1 Nitrogen oxides
Nitrogen oxides (NOx) include nitric oxide (NO) and nitrogen dioxide (NO2). Since NOx is a mixture, both NO and NO2 must be expressed on an NO2-equivalent basis before the individual quantities are combined for the total NOx release. Do not include nitrous oxide (N2O) when calculating NOx releases.
8.2 Sulphur dioxide
Sulphur dioxide (SO2) is part of the sulphur oxide (SOx) family of gases. However, reporting to the NPRI is only required for SO2, not SOx. Therefore, the quantity of the other gases in the SOx family, (i.e., sulphite, sulphur trioxide [SO3] and sulphate [SO4]) released should not be considered when calculating SO2 releases.
8.3 Particulate matter
Three size fractions of particulate matter (PM) are required to be reported to the NPRI:
- total PM with a diameter less than 100 micrometres (TPM)
- PM with a diameter less than or equal to 10 micrometres (PM10)
- PM with a diameter less than or equal to 2.5 micrometres (PM2.5)
The TPM fraction includes PM10 and PM2.5, while PM10 includes PM2.5. It is therefore impossible for PM2.5 or PM10 releases to exceed TPM releases. It is also impossible for PM2.5 releases to exceed PM10 releases.
Only filterable PM is reportable to the NPRI; condensable PM should not be included in release calculations. If the best available estimation method includes both filterable and condensable PM, and it is not possible to determine how much of the quantity is condensable PM to remove from the total, then the total can be reported. Facilities are required to indicate whether their reported PM quantities include condensable PM and can include a comment in the reporting system to provide more information.
Filterable particulate matter is particles that are directly emitted by a source as a solid or liquid (aerosol) at stack or release conditions and that are captured on the filter of a stack test sampling train. Filterable PM is a component of primary PM.
Condensable particulate matter (CPM) is material that is a vapor at stack conditions, but that condenses and/or reacts upon cooling and dilution in ambient air to form solid or liquid PM immediately after discharge from the stack. CPM is a component of primary PM. All CPM is assumed to be in the PM2.5 fraction.
TPM, PM10 and PM2.5 releases from road dust caused by vehicular traffic on unpaved roads within facility boundaries are required to be included in release calculations, when travel on these roads is ≥ 10,000 vehicle kilometres travelled per year, where the air release threshold is also met.
8.4 Volatile organic compounds (total)
Volatile organic compounds (VOCs) are an aggregate grouping of more than 1,000 organic substances that readily volatilize and undergo photochemical reactions in the atmosphere.
VOCs (total) should be reported as the total quantity of VOCs that participate in atmospheric photochemical reactions. Do not include any of the 63 substances or groups of substances that are specified in Schedule 1 of CEPA as being excluded from the VOC definition (Table 5).
| CAS RN | CEPA Schedule 1 number | Substance name |
|---|---|---|
| 74-82-8 | (a) | methane |
| 74-84-0 | (b) | ethane |
| 75-09-2 | (c) | methylene chloride (dichloromethane) |
| 71-55-6 | (d) | 1,1,1-trichloroethane (methyl chloroform) |
| 76-13-1 | (e) | 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113) |
| 75-69-4 | (f) | trichlorofluoromethane (CFC-11) |
| 75-71-8 | (g) | dichlorodifluoromethane (CFC-12) |
| 75-45-6 | (h) | chlorodifluoromethane (HCFC-22) |
| 75-46-7 | (i) | trifluoromethane (HFC-23) |
| 76-14-2 | (j) | 1,2-dichloro-1,1,2,2-tetrafluoroethane (CFC-114) |
| 76-15-3 | (k) | chloropentafluoroethane (CFC-115) |
| 306-83-2 | (l) | 1,1,1-trifluoro-2,2-dichloroethane (HCFC-123) |
| 811-97-2 | (m) | 1,1,1,2-tetrafluoroethane (HFC-134a) |
| 1717-00-6 | (n) | 1,1-dichloro-1-fluoroethane (HCFC-141b) |
| 75-68-3 | (o) | 1-chloro-1,1-difluoroethane (HCFC-142b) |
| 2837-89-0 | (p) | 2-chloro-1,1,1,2-tetrafluoroethane (HCFC-124) |
| 354-33-6 | (q) | pentafluoroethane (HFC-125) |
| 359-35-3 | (r) | 1,1,2,2-tetrafluoroethane (HFC-134) |
| 420-46-2 | (s) | 1,1,1-trifluoroethane (HFC-143a) |
| 75-37-6 | (t) | 1,1-difluoroethane (HFC-152a) |
| 98-56-6 | (u) | parachlorobenzotrifluoride (PCBTF) |
| various | (v) | cyclic, branched, or linear completely methylated siloxanes |
| 67-64-1 | (w) | acetone |
| 127-18-4 | (x) | perchloroethylene (tetrachloroethylene) |
| 422-56-0 | (y) | 3,3-dichloro-1,1,1,2,2-pentafluoropropane (HCFC-225ca) |
| 507-55-1 | (z) | 1,3-dichloro-1,1,2,2,3-pentafluoropropane (HCFC-225cb) |
| 138495-42-8 | (z.1) | 1,1,1,2,3,4,4,5,5,5-decafluoropentane (HFC-43-10mee) |
| 75-10-5 | (z.2) | difluoromethane (HFC-32) |
| 353-36-6 | (z.3) | ethylfluoride (HFC-161) |
| 690-39-1 | (z.4) | 1,1,1,3,3,3-hexafluoropropane (HFC-236fa) |
| 679-86-7 | (z.5) | 1,1,2,2,3-pentafluoropropane (HFC-245ca) |
| 24270-66-4 | (z.6) | 1,1,2,3,3-pentafluoropropane (HFC-245ea) |
| 431-31-2 | (z.7) | 1,1,1,2,3-pentafluoropropane (HFC-245eb) |
| 460-73-1 | (z.8) | 1,1,1,3,3-pentafluoropropane (HFC-245fa) |
| 431-63-0 | (z.9) | 1,1,1,2,3,3-hexafluoropropane (HFC-236ea) |
| 406-58-6 | (z.10) | 1,1,1,3,3-pentafluorobutane (HFC-365mfc) |
| 593-70-4 | (z.11) | chlorofluoromethane (HCFC-31) |
| 1615-75-4 | (z.12) | 1-chloro-1-fluoroethane (HCFC-151a) |
| 354-23-4 | (z.13) | 1,2-dichloro-1,1,2-trifluoroethane (HCFC-123a) |
| 163702-07-6 | (z.14) | 1,1,1,2,2,3,3,4,4-nonafluoro-4-methoxy-butane (C4F9OCH3) |
| 163702-08-7 | (z.15) | 2-(difluoromethoxymethyl)-1,1,1,2,3,3,3-heptafluoropropane ((CF3)2CFCF2OCH3) |
| 163702-05-4 | (z.16) | 1-ethoxy-1,1,2,2,3,3,4,4,4-nonafluorobutane (C4F9OC2H5) |
| 163702-06-5 | (z.17) | 2-(ethoxydifluoromethyl)-1,1,1,2,3,3,3-heptafluoropropane ((CF3)2CFCF2OC2H5) |
| 79-20-9 (and various) | (z.18) | methyl acetate and perfluorocarbon compounds (various classes) |
| 375-03-1 | (z.19) | 1,1,1,2,2,3,3-heptafluoro-3-methoxy-propane (HFE-7000) |
| 297730-93-9 | (z.20) | 3-ethoxy-1,1,1,2,3,4,4,5,5,6,6,6-dodecafluoro-2-(trifluoromethyl) hexane (HFE-7500) |
| 431-89-0 | (z.21) | 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea) |
| 107-31-3 | (z.22) | methyl formate (HCOOCH3) |
| 540-88-5 | (z.23) | t-butyl acetate |
| 132182-92-4 | (z.24) | 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-trifluoromethyl-pentane (HFE-7300) |
| 108-32-7 | (z.25) | propylene carbonate |
| 616-38-6 | (z.26) | dimethyl carbonate |
| 29118-24-9 | (z.27) | trans-1,3,3,3-tetrafluoropropene (HFO-1234ze) |
| 1691-17-4 | (z.28) | HCF2OCF2H (HFE-134) |
| 78522-47-1 | (z.29) | HCF2OCF2OCF2H (HFE-236cal2) |
| 188690-78-0 | (z.30) | HCF2OCF2CF2OCF2H (HFE-338pcc13) |
| 188690-77-9 | (z.31) | HCF2OCF2OCF2CF2OCF2H |
| 754-12-1 | (z.32) | 2,3,3,3-tetrafluoropropene (HFO-1234yf) |
| 102687-65-0 | (z.33) | trans 1-chloro-3,3,3-trifluoroprop-1-ene [HCFO-1233zd(E)] |
| 124-68-5 | (z.34) | 2-amino-2-methyl-1-propanol |
VOCs are listed in Parts 1, 2, 4 and 5 of the NPRI. When reporting VOCs, it is important to note the following:
- total organic compounds (TOCs) and VOCs do not have the same definition:
- all VOCs can be considered TOCs, however, not all TOCs are considered VOCs.
- base the VOC emissions on the total mass of all VOC substances emitted annually
- Part 1 of the substance list includes 93 substances or groups of substances that meet the VOC definition:
- individual reports must be submitted for each of these VOCs that meet the Part 1 criteria (based on quantities manufactured, processed or otherwise used)
- regardless of whether the Part 1 criteria are met, any releases to air of these substances must also be included in threshold calculations for Part 4 VOCs, along with all other VOCs emitted
- five of the PAHs listed in Part 2 also meet the CEPA definition of a VOC (acenaphthene, acenaphthylene, anthracene, fluorene, and phenanthrene)
- these PAHs must be included in the calculation for total Part 4 VOCs, and are also subject to Part 2
- when calculating Part 4 total VOCs, include any substance that meets the CEPA definition of VOC, even if it is not listed separately in Part 1 or Part 5
- in addition to total VOCs, facilities may be required to report additional information on speciated VOCs listed in Part 5 (see section 9 for more information)
- eighteen VOCs are listed on both Part 1 and Part 5 and are subject to reporting requirements for both Parts
8.5 Reporting criteria for Part 4 substances for Case 1 and 2 facilities
The criteria for reporting Part 4 substances and the information to be reported vary depending on the number of employees and the activities that take place at the facility. Facilities can belong to one of the four categories, or “cases”. Case 1 and 2 facilities can be classified under any NAICS code and the criteria for reporting for these facilities are described below:
A facility is Case 1 if:
- it is not a pipeline installation and either:
- activities to which the employee threshold does not apply takes place (see section 3.4.3)
- employees work a total ≥ 20,000 hours during the calendar year
A facility is Case 2 if any of the following apply:
- the facility is a pipeline installation where stationary combustion equipment is operated (see section 3.4.2 for the definition of a pipeline installation)
- employees do not work a total < 20,000 hours during the calendar year and:
- no activities to which the employee threshold does not apply take place
- the facility is not in the oil and gas extraction (except oil sands) sector (NAICS 211110)
- the facility is in the oil and gas extraction (except oil sands) sector (NAICS 211110) and consists solely of compression equipment
Case 3 and Case 4 facilities are facilities in the oil and gas extraction (except oil sands) sector (NAICS 211110) and do not meet the employee threshold. Requirements for Case 3 and 4 facilities are not described further in this Guide. For more information on the reporting requirements for oil and gas facilities, see the Oil and gas industry: guide to reporting.
In contrast to the majority of NPRI substances, the thresholds for CAC emissions are based on the quantity released to air. In general, any person who owns or operates a contiguous facility, a portable facility, a pipeline installation or an offshore installation must report for a Part 4 substance if:
| Criteria air contaminant (CAC) | Release threshold (tonnes) |
|---|---|
| Nitrogen oxides (expressed as nitrogen dioxide) | 20 |
| Sulphur dioxide | 20 |
| Carbon monoxide | 20 |
| Total particulate matter | 20 |
| Volatile organic compounds (total) | 10 |
| Particulate matter ≤ 10 micrometres (PM10) | 0.5 |
| Particulate matter ≤ 2.5 micrometres (PM2.5) | 0.3 |
For the purposes of determining if Case 2 applies (and for determining which sources need to be included for threshold calculations and which sources need to be reported; see section 8.6), stationary combustion equipment is defined as follows:
8.5.1 Stationary combustion equipment
Stationary combustion equipment includes devices that combust solid, liquid, or gaseous fuel, generally for the purposes of producing electricity, generating steam, or providing useful heat or energy for industrial, commercial, or institutional use, or reducing the volume of waste by removing combustible matter. This includes any combustion equipment that needs to be stationary to function or operate properly, or is not capable of self-propulsion. Both internal and external combustion equipment are included.
- External combustion equipment
-
Any equipment with a combustion process that occurs at atmospheric pressure and with excess air including:
- heaters
- furnaces
- incinerators
- boilers
- flares
- combustion chambers
- external combustion engines such as steam engines and Stirling engines
- steam/electric generating plants
- other commercial units
- Internal combustion equipment
-
Any equipment with a combustion process that occurs in a confined space and above atmospheric pressure including:
- gas turbines
- natural-gas-fired reciprocating engines
- gasoline and diesel industrial engines
- large, stationary diesel and dual-fuel engines
8.6 Calculating releases of Part 4 substances
Case 1 facilities must include releases of CACs from all sources when determining if the air release threshold is met. Case 2 facilities are required to include only releases of CACs from stationary combustion equipment when determining if the air release threshold is met. Below are some of the most common sources of CAC emissions:
- abrasive blasting:
- the process of cleaning or texturing materials with an abrasive material such as sand, coal and smelter slag, as well as mineral, metallic or synthetic abrasives
- the blasting process itself is a source of PM emissions, especially PM10 and PM2.5
- equipment leaks:
- equipment connections, joints and interfaces can be the source of gaseous and liquid releases
- if the equipment is handling a gaseous stream containing a CAC, the gaseous leak would result in a fugitive CAC release
- depending on the properties of a liquid (such as vapour pressure, temperature and pressure), a liquid release may also result in a fugitive CAC release
- external combustion equipment:
- comprises any equipment with a combustion process that occurs at atmospheric pressure and with excess air (see section 8.5.1 for a list of included equipment)
- fermenting:
- involves the use of yeast, bacteria, enzymes, etc., to break down complex organic compounds
- many industries use fermentation including:
- production of bread
- production of spirits
- production of pharmaceuticals
- production of fuel
- production of beer and wine
- environmental bioremediation processes
- Internal combustion equipment:
- any equipment with a combustion process that occurs in a confined space and above atmospheric pressure (see section 8.5.1 for a list of included equipment)
- loading and unloading:
- fugitive CAC emissions can result from the loading and unloading of vehicles or containers
- if the material being transferred is a liquid, the resulting emissions would likely be in the form of VOCs
- if the material is a solid, the resulting emissions would likely be in the form of PM
- painting:
- VOCs are released from paint during its application and drying
- PM2.5 may also be emitted if paint is applied by pulverization
- this category includes:
- the painting of vehicles
- furniture
- storage tanks
- any other painted product
- printing:
- VOCs are released from fixers, developers and solvents used during printing processes
- road dust:
- TPM, PM10 and PM2.5 releases from road dust caused by vehicular traffic on unpaved roads within facility boundaries are required to be included in release calculations, when travel on these roads is ≥ 10,000 vehicle kilometres travelled per year
- solvent use:
- includes, but is not limited to:
- solvent degreasing
- waste solvent reclamation
- product formulation
- commercial solvent use
- includes, but is not limited to:
- stationary combustion equipment:
- comprises any combustion equipment that needs to be stationary to function or operate properly, or is not capable of self-propulsion
- includes both internal and external combustion equipment
- storage piles:
- generate PM emissions
- pile moisture content, wind speed, and proportion of aggregate fines influence total emissions from a storage pile
- storage tanks:
- comprise any storage tanks containing:
- fuels
- solvents
- hydrocarbons
- paints
- other solutions that contain VOCs
- this includes:
- fixed roof tanks
- external floating roof tanks
- domed external floating roof tanks
- internal floating roof tanks
- variable vapour space tanks
- pressure storage tanks
- comprise any storage tanks containing:
Flow for reporting Part 4 substances
Step 1: Confirm if all of these statements apply:
- CACs are released to air only from stationary, external combustion equipment
- the cumulative nameplate capacity of that equipment is < 10 million BTU/hour
- only commercial grade natural gas, liquefied petroleum gas, Number 1 or 2 fuel oil, or any combination thereof is combusted
Yes: The owner/operator is not required to submit a report for Part 4 substances.
No: Continue to Step 2.
Step 2: Confirm which "Case" applies (see section 8.5).
Step 3: Confirm if one or more CACs were released to air in a quantity ≥ to its release threshold (see Table 6)
- for Case 1 facilities include all releases of CACs from all sources and activities
- for Case 2 facilities only include releases of CACs from stationary combustion equipment
No: The owner/operator is not required to submit a report for Part 4 substances.
Yes: The owner/ operator is required to submit a report for each Part 4 substance that was released to air in a quantity ≥ to the threshold. Continue to Step 4.
Step 4: Report for Part 4.
Case 1 facilities report releases from all sources and activities. Case 2 facilities report releases from stationary combustion equipment only.
If facility operations include one or more electricity generation units that:
- have a capacity of ≥ 25 MW
- distribute or sell to the grid ≥ 33% of its potential electrical output
The owner/operator is required to report releases to air for individual electricity generation units for each CAC that is required to be reported.
8.6.1 Possible exclusion from reporting CACs for Case 1 and 2 facilities
A facility is not required to submit a report for a CAC, if all the following criteria are met:
- the CAC is released to air only from stationary external combustion equipment
- the cumulative nameplate capacity of all stationary external combustion equipment is less than 10 million BTUs/hour (10.55 million kJ/hour)
- the only type of fuel combusted in that equipment is:
- commercial grade natural gas
- liquefied petroleum gas
- Number 1 or 2 fuel oil
- any combination thereof
This exclusion does not apply if any other fuels are burned in the stationary external combustion equipment.
For the purposes of determining whether or not this exclusion applies, stationary external combustion equipment and nameplate capacity are defined as follows:
- Stationary external combustion equipment
- Any stationary equipment with a combustion process that occurs at atmospheric pressure and with excess air. This may include thermal electric generating plants, industrial boilers, and commercial and domestic combustion units.
- Nameplate capacity
- The total designed energy input capacity of the stationary, external combustion equipment. Cumulative nameplate capacity refers to the total nameplate capacities of all stationary external combustion equipment at the facility.
8.7 Reporting releases of Part 4 substances
If the reporting criteria are met for a Part 4 substance, the releases to air of that substance must be reported in tonnes. Facilities that report for one or more CACs must also report their operating schedule (days and hours) and any periods of one week or longer where the facility was shut down.
Case 1 facilities must report all releases from all sources. Case 2 facilities should only report releases from stationary combustion equipment.
Case 1 and 2 facilities may also be required to report CAC releases separately from individual stacks if certain thresholds are met (see Appendix D).
9. Reporting for Part 5 substances – Speciated volatile organic compounds
Part 5 lists 62 VOCs, collectively referred to as “speciated VOCs” (see the NPRI substance list for the complete list).
9.1 Reporting criteria for Part 5 substances
Like Part 4 substances, speciated VOCs must be reported based on quantities released to air. In general, any person who owns or operates a contiguous facility, a portable facility, a pipeline installation or an offshore installation must submit a report to the NPRI for a Part 5 substance if the total quantity of the Part 5 substance released to air is ≥ 1 tonne.
Section 8.5 above describes the four categories of facilities, or “cases,” that determine which sources must be included in threshold calculations.
Case 1 facilities must include all releases of speciated VOCs from all sources and activities. If one or more of these Speciated VOCs was released in a quantity ≥ 1 tonne, the owner/operator is required to:
- submit a report for each Part 5 substance that was released to air in a quantity ≥ 1 tonne
- report releases from all sources and activities
Case 2 facilities must include all releases of speciated VOCs only from stationary combustion equipment when determining whether the threshold for a Part 5 substance is met. If one or more of these Speciated VOCs was released in a quantity ≥ 1 tonne, the owner/operator is required to:
- submit a report for each Part 5 substance that was released to air in a quantity ≥ 1 tonne
- report releases from stationary combustion equipment only
Case 3 and Case 4 facilities are facilities in the oil and gas extraction (except oil sands) sector (NAICS 211110) that do not meet the employee threshold. For more information on the reporting requirements for oil and gas facilities, see the Oil and gas industry: guide to reporting.
9.2 Part 5 substance qualifiers
Some Part 5 substances and groups of substances are qualified in terms of what needs to be included when calculating releases. The qualifiers, described below, determine whether a report will be required for a given substance. Supplemental information on speciated VOCs and their isomers is presented in Appendix E.
"all isomers"
Butyl acetate:
- includes:
- n-butyl acetate (CAS RN 123-86-4)
- isobutyl acetate (CAS RN 110-19-0)
- sec-butyl acetate (CAS RN 105-46- 4)
- excludes tert-butyl acetate (CAS RN 540-88-5)
Ethyltoluene includes the total of all isomers of ethyltoluene:
- 2-ethyltoluene (CAS RN 611-14-3)
- 3-ethyltoluene (CAS RN 620-14-4)
- 4-ethyltoluene (CAS RN 622-96-8)
Hexane:
- includes the total of all isomers reported as an aggregate of the individual isomers
- excludes n-hexane (110-54-3)
Propyl acetate includes the total of all isomers of propyl acetate:
- isopropyl acetate (CAS RN 108-21-4)
- propyl acetate (CAS RN 109-60-4)
Trimethylbenzene (CAS RN 25551-13-7):
- includes:
- 1,2,3-trimethylbenzene (526-73-8)
- 1,3,5-trimethylbenzene (108-67-8)
- excludes 1,2,4-trimethylbenzene (95-63-6)
Xylene (CAS RN 1330-20-7) includes the total of all isomers of xylene:
- m-xylene (CAS RN 108-38-3)
- o-xylene (CAS RN 95-47-6)
- p-xylene (CAS RN 106-42-3)
The following substances include the total of all isomers reported as an aggregate of the individual isomers:
- butane
- butene (25167-67-3)
- cycloheptane
- cyclohexene
- cyclooctane
- decane
- heptane
- hexene (25264-93-1)
- methylindan (27133- 93-3)
- nonane
- octane
- pentane
- pentene
- propylene glycol methyl ether acetate (108-65-1)
"and their isomers"
Other glycol ethers and acetates include the total of the following CAS RNs and their isomers:
- 112-07-2
- 112-15-2
- 112-25-4
- 112-34-5
- 5131-66-8
- 107-98-2
- 109-59-1
- 111-90-0
- 124-17-4
- 1569-01-3
- 1569-02-4
- 2807-30-9
- 29911-27-1
- 29911-28-2
- 34590-94-8
- 54839-24-6
- 623-84-7
- 88917-22
Note that there is some overlap between the individual substances, isomer groups and other groups and mixtures listed in Part 5. For example, all isomers of decane are C10 hydrocarbons, therefore they also meet the definition of analytically unresolved hydrocarbons (C10 to C16+) (URHCs). URHCs are an agglomeration of volatile organic compounds in the C10 to C16+ range that could not be separated into individual components by the selected gas chromatography column.
Where there is overlap between different sections of the Part 5 list, information on individual substances should be reported if it is available. If information on individual substances is not available, but information on the total for an isomer group is available, the total for the isomer group should be reported. If information on the individual substance and the isomer group is not available, then information on URHCs should be reported if this range of species is appropriate.
Do not report the same quantity of a substance more than once within Part 5. For example, if the quantity of isomers of decane released to air is included as part of the total amount reported for isomers of decane, do not include that same quantity in the reported amount of URHCs.
Also note that there are 143 VOCs listed in Parts 1 and 2 of the NPRI substance list, many of which are C10 to C16+ hydrocarbons. If thresholds are met for these substances, they should be reported in both Part 1 or 2 and Part 5 (either as an individual substance or isomer group that is on the Part 5 list, or as part of URHCs). For example, if the Part 1 threshold for naphthalene (C10H8) is met, releases of naphthalene must be reported under Part 1. Since naphthalene is not listed individually in Part 5, the quantity of naphthalene released to air should be included in the total URHCs reported under Part 5, if the thresholds for Parts 4 and 5 are met. In this case, the same quantity of naphthalene that is released to air will be reported twice.
9.3 Calculating releases of Part 5 substances
Case 1 facilities must include releases of speciated VOCs from all sources when determining if the air release threshold is met. Case 2 facilities are required to include only releases of speciated VOCs from stationary combustion equipment when determining if the air release threshold is met.
Exclusion from reporting VOCs for Case 1 and 2 facilities
A facility is not required to submit a report for VOCs, if all the following criteria are met:
- the VOC is released to air only from stationary external combustion equipment
- the cumulative nameplate capacity of all stationary external combustion equipment is less than 10 million BTUs/hour (10.55 million kJ/hour)
- the only type of fuel combusted in that equipment is commercial grade natural gas, liquefied petroleum gas, Number 1 or 2 fuel oil, or any combination thereof
This exclusion does not apply if any other fuels are burned in the stationary external combustion equipment.
For the purposes of determining whether or not this exclusion applies, stationary external combustion equipment and nameplate capacity are defined as follows:
Stationary external combustion equipment: Any stationary equipment with a combustion process that occurs at atmospheric pressure and with excess air. This may include thermal electric generating plants, industrial boilers, and commercial and domestic combustion units.
Nameplate capacity: The total designed energy input capacity of the stationary, external combustion equipment. Cumulative nameplate capacity refers to the total nameplate capacities of all stationary external combustion equipment at the facility.
9.4 Reporting releases of Part 5 substances
If the reporting criteria are met for a Part 5 substance, the releases to air of that substance must be reported in tonnes.
Case 1 facilities must report all releases from all sources. Case 2 facilities should only report releases from stationary combustion equipment.
Case 1 and 2 facilities may also be required to report speciated VOC releases separately from individual stacks if certain thresholds are met (see Appendix D).
Unlike Parts 1 through 4 substances, where releases to air must be reported separately in several categories (i.e., stack or point releases, storage tank and related handling releases, fugitive releases, etc.; see section 10.3), releases of speciated VOCs must be reported as
- The total for each individual stack that meets thresholds (see Appendix D)
- The total of all other releases that are not from individual stacks that meet thresholds
10.1 Types of facilities
- Contiguous facility
- All buildings, equipment, structures and stationary items that are located on a single site, or on contiguous sites or adjacent sites, that are owned or operated by the same person and that function as a single integrated site, including wastewater collection systems that release treated or untreated wastewater into surface waters.
- Offshore installation
- An offshore drilling unit, production platform or ship, or subsea installation that is related to the exploitation of oil or natural gas and that is attached or anchored to the continental shelf of Canada or within Canada’s exclusive economic zone.
- Pipeline installation
- A collection of equipment, situated at a single site, used in the operation of a natural gas transmission or distribution pipeline. This definition includes pipeline compressor and storage stations along pipelines used to transport raw or processed natural gas. Pipeline installations are subject only to the reporting criteria for CACs (Part 4 substances) and speciated VOCs (Part 5 substances).
- Portable facility
- Portable polychlorinated biphenyl (PCB) destruction equipment, portable asphalt plants and portable concrete batching plants. The definition applies where the facility can be entirely relocated for operation. The owner or operator of a portable facility will submit a report for the location where the facility operated for the longest period of time in the calendar year, using the total quantity of releases, disposals, or transfers from all operating locations. For all other locations where the portable facility operated during the year, the dates, addresses and geographic coordinates are to be submitted in the facility comments section in the online reporting system.
- Compressor station
- A facility where gas pressure is increased to overcome friction losses through a pipeline or pipe system or for underground natural gas storage.
10.2 Manufacture, process and otherwise use
- Manufacture
- Manufacture means to produce, prepare or compound an NPRI substance. It also includes the incidental production of an NPRI substance as a by-product. The production of chlorine dioxide by a chemical plant is an example of manufacturing. The production of hydrochloric acid during the manufacture of chlorofluorocarbons is an example of the incidental manufacture of hydrochloric acid.
- Process
- Process means the preparation of an NPRI substance, after its manufacture, for distribution in commerce. Processing includes the preparation of a substance with or without changes in physical state or chemical form. The term also applies to the processing of a mixture or formulation that contains an NPRI substance as one component, the processing of articles (see section 10.7), and the processing of a substance as a by-product. The use of chlorine to manufacture hypochloric acid (not an NPRI substance) is an example of processing of chlorine. The use of toluene and xylene to blend paint solvent mixtures is an example of processing without changes in chemical form.
- Otherwise use
- Otherwise use (or other use) means any use, disposal or release of an NPRI substance that does not fall under the definitions of manufacture or process. This includes the use of the substance as a chemical processing aid, manufacturing aid or some other ancillary use, and the other use of by-products. For example, the use of trichloroethylene in the maintenance of manufacturing and process equipment is an example of an “other use” of that substance. Certain specified uses of substances are excluded and are listed in section 3.5.2 and section 3.5.3.
10.3 Release, disposal, and recycling categories
10.3.1 On-site releases
A discharge of a substance to the environment within the physical boundaries of the facility. This includes releases to air, surface waters and land. Routine releases (e.g., fugitive releases) and accidental or non-routine releases (e.g., spills) are included. Releases do not include on-site or off-site disposals or off-site transfers for recycling.
Releases to air
- Stack or point releases
-
Controlled releases to air that occur through confined air streams, including releases from stacks and flares, and controlled venting through ducts or pipes (local exhaust ventilation systems that capture process-generated emissions at the source and then vent to the atmosphere). Releases to air from pollution control equipment generally fall into this category. Examples of stack or point releases:
- boilers
- engines
- flares
- incinerators
- kilns
- furnaces
- Storage tank and related handling releases
-
Releases resulting from the storage of liquids in tanks, including:
- releases associated with liquid storage tank operations
- releases from the transfer, loading and unloading of liquids to and from storage tanks
- losses associated with the storage of liquids in tanks
- losses associated with the cleaning, degassing and maintenance of storage tanks
Examples of storage and related handling releases:
- working and breathing losses
- tank roof landing losses,
- flashing losses
- degassing and cleaning losses
All other releases that result from storage or handling should be reported as either stack or point releases or fugitive releases.
- Fugitive releases
-
Releases to air that do not occur through a confined air stream, i.e., releases that could not reasonably pass through a stack, chimney, vent, or other functionally equivalent opening designed to direct or control its flow. Also includes individual small release points that cannot be practically inventoried separately because they are too small, too numerous or too geographically dispersed. Examples of fugitive releases:
- fugitive equipment leaks from valves, pump seals, flanges, compressors, sampling connections, open-ended lines, etc.
- evaporative losses from surface impoundments
- evaporative losses from spills or leaks to land or water
- spills (accidental releases) directly to air must be reported under the spills to air category
- releases from building general exhaust ventilation systems that use dilution air to disperse and exhaust process emissions
- uncontrolled releases from enclosed storage of solids inside silos and bunkers, and related transfer and loading/unloading operations (e.g., grain elevators)
- any other fugitive or non-point stationary air emissions from:
- land treatment
- tailings
- waste rock
- mine faces
- pit faces
- open conveyor transfer points
- open storage piles loading and unloading
- wind erosion from open storage piles and open areas
- materials handling (that is not related to the storage of liquids in tanks)
- space heating
- cooling towers
- solvent use
- wastewater treatment
- other sources
- Spills or other accidental releases
-
Accidental uncontrolled releases to air. Spills differ from fugitive releases since they normally occur over a short period of time (hours or days), whereas fugitive releases are chronic events that occur over a comparatively longer period of time (months or years). Examples of spills or other accidental releases:
- releases occurring during a process upset
- releases from a pipeline rupture that occur over a short period of time
- releases resulting from an accidental explosion or fire
- Unpaved road dust
- total particulate matter, PM10 and PM2.5 releases from road dust must be reported if vehicles travelled more than 10,000 kilometres on unpaved roads at the facility.
- Other non-point releases
-
Any other non-point releases to air that are not captured in the categories above. Note that it is extremely unlikely that a release to air could not fall under one of the categories listed above. Releases should only be reported under the “other non-point releases” category after careful consideration of the other categories. Detailed comments should be provided to explain why releases were reported as “other non-point releases.”
The following points provide additional context about the air release categories and their relationship to one another:
- all releases to air are either point or fugitive
- some subsets of point and fugitive releases to air must be reported separately to the NPRI:
- releases from storage of liquids in tanks could be point or fugitive, but get reported under the “storage tank and related handling releases” category
- road dust is always fugitive but gets reported under the road dust category
- the category for “other non-point releases to air” should not be used, since releases to air are always either point, fugitive or part of one of the specified subsets of releases
Note that there may be specific circumstances where sources could either be reported as stack or point sources or fugitive sources. For example, large stand-alone cooling towers would be reported as stack or point sources (and may be subject to the individual stack reporting requirements if they are 25 m or more in height above grade; see Appendix D), whereas a collection of smaller rooftop cooling towers may be reported as fugitive sources. Emissions from a single large backup generator could be reported as stack or point releases, whereas a number of smaller backup generators dispersed throughout the facility property would be reported as fugitive releases.
Releases to surface waters
Releases to oceans, lakes, wetlands, rivers, streams, etc. are included.
- Direct discharges
-
Releases that are directly discharged to surface waters (such as a river, lake or ocean) from within the site boundaries:
- these discharges typically occur through a pipe, ditch, or other similar conveyance system but can also include uncontrolled run-off
- this category includes discharges from on-site wastewater treatment systems as well as discharges that leave the facility and do not feed into an off-site wastewater facility before reaching surface waters
- discharges to municipally owned sewer systems (regardless of the level of treatment) or other off-site wastewater treatment facilities are to be reported as off-site transfers for treatment prior to final disposal
- Spills
- Include any accidental releases to surface waters, normally occurring over a short period of time (hours or days)
- Leaks
- Leaks differ from spills in that they are chronic events, occurring over a comparatively long time (weeks, months, etc.)
Releases to land
Releases to land include surface and underground releases which occur at a facility.
- Spills
- Include any accidental releases to land, normally occurring over a short period of time (hours or days)
- Leaks
- Leaks differ from spills in that they are chronic events, occurring over a comparatively long time (days, months, etc.)
- Other releases to land that are not disposals
-
Net quantities of other releases to land that are not spills or leaks and are not for the purposes of disposal:
- this category includes NPRI substances that are injected underground for purposes other than disposal (for example, solvents used to enhance in situ bitumen extraction)
- NPRI substances sent to landfill, used for land application, disposed of by underground injection, or transferred for treatment or storage are categorized as disposals (see the following sections for more information on disposals)
- disposal quantities should be reported under the disposal category only, and not under releases to land, to avoid double-reporting
10.3.2 Disposals
The final disposal to landfill, land application or underground injection, either on the facility site or at a location off the facility site; transfer to a location off the facility site for storage or treatment prior to final disposal; or movement into an area where tailings or waste rock are discarded or stored, and further managed to reduce or prevent releases to air, water or land, either on the facility site or at a location off the facility site. The disposal of a substance is different from a direct release to air, water or land.
On-site disposals
- Landfill
- Total quantities of substances sent for final disposal to a designated landfill area located within the site boundaries.
- Land application
- Total quantities of substances sent for final disposal by application or incorporation into soil within the site boundaries.
- Underground injection
- Total quantities of substances disposed of by injection underground from within the site boundaries.
- Tailings and waste rock
- Net quantities of substances that are moved into an on-site area where tailings or waste rock are discarded or stored and further managed to reduce or prevent releases.
Off-site disposals
Off-site disposals include total quantities that are transferred off the facility site for final disposal.
- Landfill
- Total quantities of substances sent for final disposal to a designated landfill area located outside the site boundaries.
- Land application
- Total quantities of substances sent for final disposal by application or incorporation into soil outside the site boundaries.
- Underground injection
- Total quantities of substances sent for final disposal by injection underground from outside the site boundaries.
- Storage off-site prior to final disposal
- Quantities of substances that are transferred to an off-site area for storage prior to final disposal.
- Tailings and waste rock
- Quantities of substances that are transferred to an off-site area where tailings or waste rock are discarded or stored and further managed to reduce or prevent releases.
Tailings and waste rock
- Inert waste rock
-
Waste rock that either:
- is inert or clean according to a federal or provincial operating permit
- has a sulphur concentration of ≤ 0.2%
- has a sulphur concentration of > 0.2% and the ratio of neutralizing potential to acid generating potential is ≥ 3:1
- Tailings
-
The waste material (which may or may not be mixed with water) that remains after processing of ore or mined materials, in order to extract marketable components such as metals, minerals or bitumen. This can include:
- ground rock material
- sand
- clay
- process chemicals or residual metals
- minerals or bitumen
- pretroleum coke (petcoke)
- sulphur
- Unconsolidated overburden
-
Unconsolidated materials overlying the ore or bitumen deposit, including, but not limited to:
- soil
- glacial deposits
- sand
- sediment
- Waste rock
- Rock that is removed in the mining process to provide access to the ore and is not further processed during the reporting year. Waste rock does not include unconsolidated overburden.
10.3.3 Transfers
An NPRI-listed substance may be transferred to a location off the facility site for treatment prior to final disposal or for recycling and energy recovery.
Off-site transfers for treatment prior to final disposal
Treatment means subjecting the substance to physical, chemical, biological or thermal processes.
- Physical treatment
-
A treatment process in which the substance is separated from the waste product by various physical methods, such as:
- drying
- evaporation
- encapsulation
- vitrification
- Chemical treatment
-
A treatment process in which the substance is altered by a chemical reaction to destroy the hazardous component, such as:
- precipitation
- stabilization
- neutralization
- Biological treatment
- A treatment process in which bacteria, fungi, and or/microorganisms are used to alter or destroy the substance, such as bio-oxidation.
- Incineration or thermal treatment, where energy is not recovered
- A treatment process involving the decomposition of the substance by thermal means to less hazardous or nonhazardous components.
- Treatment in a municipal wastewater treatment plant
- Transferred for treatment in a municipal wastewater treatment plant.
Off-site transfers for recycling and energy recovery
Recycling refers to activities that keep a material or a component of the material from becoming a waste destined for final disposal. Recyclable materials may be cleaned, regenerated or reprocessed to their original specifications and reused for their original purpose. They may also be used for an entirely different purpose without any pre-treatment or modification. Components may be recovered or reclaimed from the recyclable material or the material may be used as a fuel for energy recovery. The recyclable material may be used in the manufacture of another product.
For the purposes of the NPRI, recycling also includes substances sent back to a manufacturer, supplier or recycler for reprocessing, repackaging, resale or for credit or payment. For example, metal shavings or turnings that are sold to a recycler are considered to be transfers off-site for recycling. The categories of recycling listed in the NPRI are:
- energy recovery
- recovery of solvents
- recovery of organic substances (not solvents)
- recovery of metals and metal compounds
- recovery of inorganic materials (not metals)
- recovery of acids or bases
- recovery of catalysts
- recovery of pollution abatement residues
- refining or reuse of used oil
- other recovery, reuse or recycling activities
10.4 Activities to which the employee threshold does not apply
10.4.1 Incineration
A waste incinerator is a device, mechanism or structure constructed primarily to thermally treat waste for the purpose of reducing its volume, or destroying hazardous chemicals or pathogens present in the waste. This includes facilities where waste heat is recovered as a by-product from the exhaust gases of an incinerator (e.g., energy-from-waste incinerators), conical burners and beehive burners. This does not include industrial processes where fuel derived from waste is fired as an energy source, such as industrial boilers. For example, if bark, wood chips or other wood waste are used as fuel to fire a boiler, these activities are not considered energy-from-waste incinerators.
- Biomedical or hospital waste incineration
-
Biomedical or hospital waste includes:
- human anatomical waste
- animal waste
- microbiology laboratory waste
- human blood and body fluid waste
- waste sharps
It does not include waste that is:
- from animal husbandry
- household in origin
- controlled in accordance with the Health of Animals Act
Household wastes or wastes that are generated in food production, general building maintenance and office administration activities of those facilities to which this definition applies are considered to be non-hazardous waste, not biomedical or hospital waste. For more information, consult the Guide to Hazardous Waste and Hazardous Recyclable Material Classification.
- Hazardous waste incineration
- Hazardous waste includes wastes that are potentially hazardous to human health or the environment because of their nature and quantity, and that require special handling techniques. They are defined by taking into account the hazard criteria established under the Transportation of Dangerous Goods Regulations as well as wastes and materials specifically listed in the Cross-border Movement of Hazardous Waste and Hazardous Recyclable Material Regulations. This includes hazardous waste incinerated in a mobile incinerator temporarily located at a facility.
- Non-hazardous solid waste incineration
- Non-hazardous solid waste is any solid waste, regardless of origin, that, if not incinerated, might normally be disposed of in a non-secure manner (e.g., at a sanitary landfill site). It includes clean wood waste (i.e., waste from woodworking or forest product operations, including bark, where the wood waste has not been treated with preservative chemicals or decorative coatings), and residential and other municipal wastes.
- Sewage sludge incineration
- Sludge is a semi-liquid mass removed from a liquid flow of wastes. Sewage sludge is sludge from a facility treating wastewater from a sewer system. The drying of sludge to reduce water content is part of the incineration stage.
10.4.2 Other activities
- Pit
-
An excavation that is open to the air, and any associated infrastructure, that is operated for the purpose of extracting:
- sand
- clay
- marl
- earth
- shale
- gravel
- unconsolidated rock
- other unconsolidated materials that are not bitumen
Pits and quarries are only required to report if annual production is 500,000 tonnes or more. An open-pit mine that is operated for the purpose of extracting ore, bitumen, coal or other materials not listed above is not included in the definition of a pit or quarry, and the 500,000 tonnes production threshold does not apply to these facilities. For more information, consult the Pits and Quarries Reporting Guide.
- Quarry
-
An excavation that is open to the air, and any associated infrastructure, that is operated for the purpose of working, recovering or extracting:
- limestone
- sandstone
- dolostone
- marble
- granite
- other consolidated rock
Pits and quarries are only required to report if annual production is 500,000 tonnes or more. For more information, consult the Pits and Quarries Reporting Guide.
- Terminal operations
-
Terminal operations are either:
- the use of storage tanks and associated equipment at a site used to store or transfer crude oil, artificial crude or intermediates of fuel products into or out of a pipeline
- the operating activities of a primary distribution installation, normally equipped with floating roof tanks, that receives gasoline by pipeline, railcar, marine vessel or directly from a refinery
Terminal operations do not include bulk plants or service stations.
- Wastewater collection systems
- A wastewater collection system includes both the collection components (a system of sewers and/or ditches that convey sanitary or combined sewage for a community) and treatment components (a plant or process location that accepts collection system flows for the purposes of removing substances from the wastewater). A wastewater collection system that discharges treated or untreated wastewater to surface waters is required to report if the annual average discharge rate is 10,000 cubic metres or more per day. Note that this discharge rate threshold does not apply to industrial wastewater treatment facilities. For more information, consult the Reporting guidance for the wastewater sector to the National Pollutant Release Inventory.
- Wood preservation
- Wood preservation is the use of a preservative for the preservation of wood by means of heat or pressure treatment, or both. It includes the manufacture, blending or reformulation of wood preservatives for that purpose. For more information, consult the Guidance for wood preservation facilities reporting to the NPRI.
10.5 Activities that trigger reporting of Part 3 substances (dioxins, furans and hexachlorobenzene), if the employee threshold is met
10.5.1 Combustion
- Combustion of fossil fuel in a boiler unit, with a nameplate capacity of ≥ 25 megawatts of electricity, for the purpose of producing steam for the production of electricity
- This activity includes fossil fuel combustion at electric power generation utilities and large industrial facilities co-generating electric power using waste heat from industrial processes. For the purposes of reporting to the NPRI, fossil fuel is fuel that is in a solid or liquid state at standard temperature and pressure, such as coal, petroleum or any fuel derivatives that are liquid or solid. It does not include natural gas or other fuels that are gases at ambient pressure and temperature. Fuel combustion in diesel generators is not included in this activity.
- Combustion of fuel in kraft liquor boilers used in the pulp and paper sector
- A kraft liquor boiler burns black liquor, composed mostly of lignin, which is the residue from the digester in a kraft (sulphate) pulping process. The boiler recovers chemical products from the combusted black liquor, which are later recycled. It also produces steam, which is used in mill process operations.
- Combustion of hog fuel originating from logs that were transported or stored in salt water in the pulp and paper sector
- Pulp and paper boilers burning salt-laden wood are unique to British Columbia. Dioxins and furans are emitted from the burning of salt-contaminated hog fuel. Chlorine is absorbed by the bark of logs transported and stored in salt water. The bark stripped from logs is ground up with other waste wood to produce hog fuel, which is used as boiler fuel to produce heat and electrical energy.
10.5.2 Smelting
Smelting is the melting of raw or scrap materials to produce metal for further processing into metal products. The smelting process is typically accompanied by a chemical change in which impurities are removed.
- Base metals smelting
- “Base metals” refer to copper, lead, nickel or zinc. Base metals smelting does not include smelting of aluminum, secondary lead or any other metals.
- Smelting of secondary aluminum
- “Secondary aluminum” refers to aluminum-bearing scrap or materials. Secondary aluminum smelting involves pre-cleaning and smelting, both of which may produce emissions of dioxins and furans.
- Smelting of secondary lead
- “Secondary lead” refers to lead-bearing scrap or materials, other than lead-bearing concentrates, derived from a mining operation. Facilities engaged in smelting of lead-bearing concentrates derived from a mining operation are considered to be base metal smelters.
10.5.3 Manufacturing/production
- Production of iron ore pellets using an induration furnace or manufacturing of sinter using the iron sintering process
- Sintering consists in agglomerating a fine fraction of iron-rich mill secondary materials and iron ore concentrate to become a coherent mass by heating without melting, or the growth of contact area between two or more initially distinct particles at temperatures below the melting point but above one half of the melting point. In sintering operations, dioxins and furans may be formed as by-products during high-temperature decomposition or combustion of raw materials containing chlorine and organic compounds. Pelletizing consists of agglomerating ultra-fine particles of iron ore concentrate with a binder into marble-size pellets before high temperature hardening in specialized furnaces. In these induration furnaces, dioxins and furans may be formed as by-products during high-temperature decomposition or combustion of raw materials containing chlorine and organic compounds.
- Manufacturing of Portland cement
-
Portland cement is a fine greyish powder consisting of four basic materials:
- lime
- silica
- alumina
- iron compounds
Cement production involves heating the raw materials to a very high temperature in a rotating kiln to induce chemical reactions that produce a fused material called clinker. The cement clinker is further ground into a fine powder and then mixed with gypsum to form Portland cement.
- Operation of electric arc furnaces in steel foundries and in steel manufacturing
- In an electric arc furnace, material is heated by an electric arc. Dioxins, furans and HCB may be formed as by-products during high-temperature decomposition or combustion of raw materials containing chlorine and organic compounds.
- Production of chlorinated organic solvents or chlorinated monomers
- This activity is limited to the intentional manufacturing of chlorinated organic solvents or chlorinated monomers and does not include coincidental production.
- Production of magnesium
- Production of magnesium from magnesium chloride by electrolysis may result in the generation of dioxins, furans and HCB.
- Titanium dioxide pigment production using the chloride process
- This activity is limited to titanium dioxide pigment manufactured by the chloride process, not the sulphate process.
10.6 Combustion and fuel use
10.6.1 Categories of individual stack and flare releases
- Stationary fuel combustion for energy purposes
-
Stationary fuel combustion emissions:
- emissions resulting from the oxidation of solid, liquid, and gaseous fuels from stationary fuel combustion sources for the purpose of producing heat or work (electricity and mechanical energy)
Stationary fuel combustion sources:
- stationary devices that combust either a mix of or a specific type of solid, liquid, gaseous and waste fuels for the purpose of producing heat or work (electricity and mechanical energy). This includes:
- boilers
- electricity generating units
- cogeneration units
- combustion turbines
- engines, incinerators with heat capture and use
- heaters
- kilns
- furnaces
- burners
- ovens (including coke ovens)
- dryers
- any other stationary combustion devices
Note that flares are not considered stationary fuel combustion sources.
- Combustion of fuels for non-energy purposes
-
Releases resulting from the oxidation of a fuel not for generating heat or work, for example, when the fuel is used as a reductant. When a fuel is used as both reductant and fuel in a process, the corresponding release would be considered for non-energy purposes; examples include:
- blast furnaces in iron and steel plants
- smelting of base metals
Incineration without energy recovery falls into this category.
- Flaring
-
Releases resulting from the controlled combustion of a gas or liquid stream produced at the facility, the purpose of which is not to produce useful heat or work. This includes releases from:
- waste petroleum incineration
- hazardous emission prevention systems (in pilot or active mode)
- well testing
- natural gas gathering systems
- natural gas processing plant operations
- crude oil production
- pipeline operations
- petroleum refining
- chemical fertilizer production
- steel production
- Use of fuels for non-energy products
- Releases resulting from the use of a fuel as an input to a chemical reaction to produce a non-energy product, such as the production of hydrogen (in stand-alone hydrogen plants only), ammonia or ethylene.
- Releases from all other sources not included in the above categories
- Any other activities that generate stack releases that are not covered under one of the above categories. This applies to Case 1 facilities only, which must report for all sources of emissions if thresholds are met. Case 2 facilities are only required to report combustion emissions under one or more of the categories above.
10.6.2 Exclusion for reporting Part 4 substances – Case 1 and 2 facilities
- Nameplate capacity
- The total designed energy input capacity of the stationary external combustion equipment. Cumulative nameplate capacity refers to the total nameplate capacities of all stationary external combustion equipment at the facility.
- Stationary external combustion equipment
-
Any stationary equipment with a combustion process that occurs at atmospheric pressure and with excess air. This includes any combustion equipment that needs to be stationary to function or operate properly, or is not capable of self-propulsion. This may include:
- thermal electric generating plants
- industrial boilers
- commercial and domestic combustion units
10.6.3 Determining sources to include in threshold calculations and to report – Case 2 facilities
- Stationary combustion equipment
-
Devices that combust solid, liquid, or gaseous fuel, generally for the purposes of:
- producing electricity
- generating steam
- providing useful heat or energy for industrial, commercial, or institutional use
- reducing the volume of waste by removing combustible matter
This includes any combustion equipment that needs to be stationary to function or operate properly, or is not capable of self-propulsion. Both internal and external combustion equipment are included.
- External combustion equipment
-
Any equipment with a combustion process that occurs at atmospheric pressure and with excess air, including:
- heaters
- furnaces
- incinerators
- boilers
- flares
- combustion chambers
- external combustion engines such as steam engines and Stirling engines
- steam/electric generating plants
- other commercial units
- Internal combustion equipment
-
Any equipment with a combustion process that occurs in a confined space and above atmospheric pressure, including:
- gas turbines
- natural-gas-fired reciprocating engines
- gasoline and diesel industrial engines
- large, stationary diesel and dual-fuel engines
- Article
-
A manufactured item that does not result in a release or disposal of an NPRI substance when it undergoes processing or other use. When articles are processed or otherwise used, and there are no releases or disposals, or the releases are recycled with due care, the NPRI substances in that article do not need to be included in the threshold calculation. For example:
- a metal reclamation facility accepts spent lead-acid batteries for recycling, and the batteries are broken into pieces in a hammer mill and their parts (sulphuric acid, lead and plastic) are subsequently reclaimed
- the batteries lose their article status, because they are broken apart during the recycling process
- the metal reclamation facility is now required to report any NPRI substances from these batteries if the thresholds are met
- A sealed glass bulb containing mercury used in a levelling switch meets the definition of an article
- the quantity of mercury in the switch must be included in a facility’s calculation of the reporting threshold if the item loses its article status (e.g., the bulb is broken during waste management operations, thus allowing a release of mercury)
- as long as the bulbs remain intact, they are considered articles and are therefore not included in calculating the reporting threshold
- By-product
-
The quantity of an NPRI Part 1 substance that is incidentally manufactured, processed or otherwise used at the facility at any concentration, and released to the environment or disposed of. The quantity of a substance that is recycled or that remains in the final product is not considered to be a by-product for the purpose of the NPRI threshold calculation. In general, if a quantity of a substance is intentionally manufactured, processed or otherwise used at a facility, then that quantity of the substance is not a by-product, even if it is unintentionally manufactured, processed or otherwise used at another step in the process. The quantity of a substance that is a by-product must be included in the calculation of the reporting threshold, regardless of concentration. The by-product requirements only apply to Part 1 substances and are only used for the purpose of determining whether or not the mass threshold for a substance has been met. For example:
- hydrogen fluoride is incidentally manufactured and released during aluminum smelting
- the hydrogen fluoride is a by-product and must be included in the calculation of the reporting threshold, regardless of concentration
- manganese and nickel are incidentally present in coal and are therefore by-products of the coal combustion process
- during combustion, a portion of these metals is concentrated in the ash, which is disposed of, and a portion of the metals is released in stack emissions
- the weight of the metal released from the stack and in the ash sent for disposal must be included in the calculation of the reporting threshold, regardless of concentration
- metal cuttings, sent for disposal, contain alloyed chromium and nickel at a concentration of less than 1%
- the chromium and nickel are essential components of the alloy; therefore, they are not incidentally processed and are not considered to be by-products
- the chromium and nickel in the metal cuttings do not need to be included in the calculation of the reporting threshold, because the substances are present at a concentration less than the concentration threshold of 1%.
- CAS Registry Number
- CAS Registry Number, or CAS RN, refers to the Chemical Abstracts Service Registry Number.
- Due care
- Exercising due care means that the facility generated less than one kilogram of a Part 1A substance as waste during the year. There is no quantitative measure of due care in recycling Part 1B substances, because even minimal releases of these substances can cause significant adverse effects and can reasonably be expected to contribute to exceeding their low thresholds. Therefore, if an article containing a Part 1B substance is processed or otherwise used and there are releases, the Part 1B substance in the article must be included in the threshold calculation.
- Electricity generation unit
- Physically connected equipment that operates together to produce electricity for sale or distribution to the grid by means of thermal energy and is stationary when used, and is not in or on a machine that is self-propelled.
- Emission factors
- Numerical values that relate the quantity of substances emitted from a source to a common activity associated with those emissions, and that can be categorized as published emission factors or site-specific emission factors.
- Employee
- An individual employed at the facility and includes the owner of the facility who performs work on-site at the facility, and a person, such as a contractor, who, at the facility, performs work that is related to the operations of the facility, for the period of time that the person is performing that work, but does not include volunteer fire fighters.
- Full-time employee equivalent
-
The unit obtained by dividing by 2,000 hours the sum of:
- the total hours worked by individuals employed at the facility and the total hours of paid vacation and of sick leave taken by individuals employed at the facility
- the hours worked on-site at the facility by the owner of the facility, if not employed by the facility
- the hours worked on-site at the facility by a person, such as a contractor, who, at the facility, performs work related to the operations of the facility
- Level of quantification
- In respect of a substance, the lowest concentration that can be accurately measured using sensitive but routine sampling and analytical methods.
- National Pollutant Release Inventory substance identifier
- National Pollutant Release Inventory substance identifier, or NPRI substance identifier, means a unique identification number assigned by Environment and Climate Change Canada to a substance listed on the NPRI substance list where no specific CAS RN applies or where multiple CAS RNs apply.
- Parent company
- The highest-level company or group of companies that owns or directly controls the reporting facility.
- Pollution prevention
- The use of processes, practices, materials, products, substances or energy that avoid or minimize the creation of pollutants and waste, and reduce the overall risk to the environment or human health.
- Potential electrical output
- The quantity of electricity that would be generated by a unit in a calendar year if the unit were to operate at capacity at all times during that calendar year.
11. Bibliography
- American Society for Testing and Materials (2002) Standard Practice for Determination of a Pooled Limit of Quantification, D6259-98.
- Environment Canada (1997). Determination of LoQs for Measuring Hexachlorobenzene in Selected Solvents. Draft Report AAQD 97-01, Analysis and Air Quality Division, Environmental Technology Centre.
- Environment Canada (1999). Level of Quantification Determination: PCDD/PCDF and Hexachlorobenzene. Analysis and Air Quality Division, Environmental Technology Centre.
- Environment Canada (2000). Determination of Level of Quantification for Measuring HCB and PCDD/PCDF in Soil, Draft. Analysis and Air Quality Division, Environmental Technology Centre.
The complete list of NPRI substances can be found on the NPRI website and in the Canada Gazette, Part II Notice with respect to the substances in the National Pollutant Release Inventory for 2025, 2026 and 2027.
B.1 Calculating the manufacture, process or otherwise use quantity
Table 7 illustrates the calculation of the reporting threshold for a Part 1A substance. In the example, a facility has several processes in which a Part 1A substance is manufactured, processed or otherwise used. The substance is also released as a by-product and is contained in tailings and waste rock.
This example assumes that the employee threshold is met, or an activity to which the employee threshold does not apply takes place at the facility. In this case, a report is required for this substance, because the total quantity of the Part 1A substance manufactured, processed, otherwise used, and contained in tailings and waste rock at the facility exceeded 10 tonnes, as explained below.
| Material/process containing the substance | Total weight of material containing the substance (tonnes) | Concentration/equivalent weight of the substance in material/process (%) | Net weight of the substance to include in threshold calculation (tonnes) |
|---|---|---|---|
| Compound material in process stream A | 150 | 5 | 7.5 |
| Raw material in process B | 2 | 100 | 2.0 |
| Raw material in process C | 45 | 0.20 | N/A |
| By-product released from process D | 10,000 | 0.01 | 1.0 |
| Tailings | 24,000,000 | 0.00001 | 2.4 |
| Waste rock (that is not clean or inert) | 20,000,000 | 0.00002 | N/A |
Total to include in threshold calculation: 12.9 tonnes.
- In process A, the Part 1A substance is present at 5% concentration (or equivalent weight for metallic compounds) and is included in the threshold calculation
- In process B, the raw material added to the process is a pure substance
- it is included in the threshold calculation, regardless of any subsequent dilution in the process
- The weight of the substance in the raw material used in process C is not included in the threshold calculation because the concentration is less than 1%
- note that, as a report is required in this example, the releases, disposals and transfers for recycling from all processes, including process C, are required to be reported, regardless of concentration and regardless of whether or not the quantity is used in the threshold calculation
- The weight of the substance produced and released from process D is included in the calculation because it is a by-product, and the concentration threshold does not apply
- The weight of the substance contained in tailings is included in the threshold calculation because there is no concentration threshold for tailings
- The weight of the substance contained in waste rock is not included in the threshold calculation, because the concentration of the substance in the waste rock is less than 1%
- the weight of the substance in the waste rock would also not be included when calculating disposals of the substance, because the concentration is less than 1%
- The total is the value that must be compared to the 10 tonnes reporting threshold
- this value is only used to determine that a report is required for the Part 1A substance
- a subsequent calculation must be done to obtain the actual value of releases, disposals, and transfers for recycling that must be reported
B.2 Calculating releases using continuous emissions monitoring
This example estimates emissions from an oil-fired boiler that has the example continuous emission monitoring (CEM) data in Table 8.
Where:
- measured concentration = C
- calculated emission rate = CER
| Period | O2 (%V) |
Fuel rate, Qfuel (103 kg/hr) |
Stack gas flow rate, Qstack (dRm3/min) |
C SO2 (ppmvd) |
C Nox (ppmvd) |
C CO (ppmvd) |
CER SO2 (kg/hr) |
CER Nox (kg/hr) |
CER CO (kg/hr) |
|---|---|---|---|---|---|---|---|---|---|
| 1:00 | 1.5 |
15.4 | 3,576 | 799 | 175 | 20.2 | 461 | 73 | 5 |
| 1:10 | 1.7 | 16.9 | 3,855 | 830 | 186 | 23.9 | 500 | 81 | 6 |
| 1:20 | 1.4 | 15.3 | 3,433 | 755 | 155 | 19.9 | 445 | 66 | 5 |
| 1:30 | 1.6 | 16.0 | 3,720 | 821 | 175 | 20.5 | 480 | 74 | 5 |
| 1:40 | 1.5 | 16.5 | 3,760 | 814 | 164 | 19.5 | 529 | 77 | 6 |
| 1:50 | 1.5 | 16.3 | 3,754 | 825 | 158 | 29.5 | 529 | 73 | 8 |
The following equation is used to calculate emissions from the measured concentrations:
Where:
- CERx = calculated emission rate of contaminant "x", kg/hr
- Cx = Concentration of contaminant "x", ppmvd
- MWx = Molecular weight of the contaminant "x", g/g-mole
- MWSO2 = 64
- MWNOx = 46 (as MWNO2)
- MWCO = 28
- Qstack = Dry stack gas volumetric flow rate at reference conditions (101.325 kPa and 25°C), dRm3/min
- V = Volume occupied by 1 mole of ideal gas at reference conditions (24.45 litres/g-mole)
The average SO2 emissions for the 1 hour CEM period:
B.3 Calculating releases using predictive emissions monitoring
TPM emissions from a boiler firing heavy fuel oil (HFO) are estimated in this example. To use the PEM approach, a model or relationship between TPM emission rates and fuel consumption must first be developed. An example of a model relationship is shown below.
Correlate the TPM emission rates to the HFO consumption rate of the boiler in the PEM as listed in Table 9.
| HFO consumption rate (GJ/h) | TPM emission rate (kg/h) |
|---|---|
| 71 | 16 |
| 72 | 17 |
| 73 | 17 |
| 74 | 17 |
| 75 | 17 |
| 76 | 18 |
| 77 | 18 |
| 78 | 18 |
| 79 | 18 |
| 80 | 19 |
Once the predictive model has been tested and verified it can then be used along with the fuel use consumption rate to estimate annual TPM emissions from the unit. Table 10 illustrates how the predictive model is used to estimate TPM emissions for a specific time period.
| Time (hour) | Fuel rate (GJ/h) | Predicted TPM emission rate (kg/h) |
|---|---|---|
| 1 | 74 | 17 |
| 2 | 74 | 17 |
| 3 | 76 | 18 |
| 4 | 75 | 17 |
| 5 | 76 | 18 |
| 6 | 77 | 18 |
| 7 | 78 | 18 |
| 8 | 79 | 18 |
| 9 | 80 | 19 |
| 10 | 80 | 19 |
| Total for period | 769 | 179 |
| Average for period | 76.9 | 17.9 |
The general formula for estimating emissions for contaminant "x" is:
Where:
- Ex = Emission of contaminant "x", kg/year
- Ex,ave = Average emission rate of contaminant "x", kg/hr
- T = Total operating hours in a given year
Given that the above boiler unit operated under the same condition for 7,500 hours in the year, the estimated TPM emissions would be:
B.4 Calculating releases using source testing
This source testing example is based on measured concentrations of the substance in a waste stream and the volume/flow rate of that stream. A galvanizing facility discharges its wastewater to a nearby body of water. The electroplater is required to monitor this discharge once a month for various parameters, including the release of total zinc.
Step 1: Gather wastewater flow and concentration data from the monitoring results done in compliance with the municipal by-law for wastewater discharges. Analytical results for total zinc for the year are presented in Table 11.
| Day | Wastewater flow (106L/d) | Zinc concentration (μg/L) | Releases (kg |
|---|---|---|---|
| Jan. 8 | 1.57 | 918 | 1.44 |
| Feb. 12 | 1.49 | 700 | 1.04 |
| Mar. 10 | 1.58 | 815 | 1.28 |
| Apr. 15 | 1.66 | 683 | 1.13 |
| May 9 | 1.38 | 787 | 1.09 |
| Jun. 13 | 1.29 | 840 | 1.08 |
| Jul. 11 | 1.73 | 865 | 1.50 |
| Aug. 10 | 1.60 | 643 | 1.03 |
| Sept. 8 | 1.75 | 958 | 1.68 |
| Oct. 12 | 1.56 | 681 | 1.06 |
| Nov. 10 | 1.80 | 680 | 1.22 |
| Dec. 8 | 1.63 | 627 | 1.02 |
| Average | N/A | N/A | 1.21 |
Step 2: Calculate the mass loading for those days on which a zinc analysis was performed. This is done by multiplying the daily flow by the measured zinc concentration.
Step 3: Calculate annual releases. Based on an average daily release of 1.21 kg over the year and 250 days of discharge during the year, the yearly total zinc discharged to water:
B.5 Calculating releases using source testing, levels of quantification and toxic equivalency factors
At this facility, 200 tonnes of non-hazardous waste were incinerated during the year, with a waste feed rate of 100 kg/hr. The stack flow rate was 1.2 m3/s. The facility has stack testing data for dioxins/furans. The measured stack gas concentrations of dioxins/furans in the air were:
- 4.0 ng/m3 of 1,2,3,4,7,8-hexachlorodibenzo-p-dioxin
- 7.0 ng/m3 of 1,2,3,4,7,8-hexachlorodibenzofuran
- 10.0 ng/m3 of 1,2,3,6,7,8-hexachlorodibenzofuran
The facility produced 20 tonnes of incineration ash in the year which was shipped off site for disposal in a landfill. The facility has measured an average dioxins/furans concentration of:
- 2.5 mg/tonne ash of 1,2,3,4,7,8-hexachlorodibenzo-p-dioxin
- 4.6 mg/tonne ash of 1,2,3,4,7,8-hexachlorodibenzofuran
- 8.1 mg/tonne ash of 1,2,3,6,7,8-hexachlorodibenzofuran
Step 1: Determine if the equivalent measured concentration of dioxins/furans releases to air was greater than the LoQ of 32 pg TEQ/m3
This facility is required to report releases to air for the individual congeners since the measured concentration of 2,100 pg TEQ/m3 was greater than the LoQ of 32 pg TEQ/m3.
Step 2: Calculate the hours of operation
Step 3: Calculate the quantity of dioxins/furans congeners released to the air, for example, 1,2,3,4,7,8-hexachlorodibenzo-p-dioxin:
Step 4: Determine if the measured concentration of dioxins/furans in the incineration ash was greater than the LoQ of 9 pg TEQ/g ash:
The measured concentration of 1,520 pg TEQ/g ash was greater than the LoQ for dioxins/furans in ash of 9 pg TEQ/g ash; therefore the quantity of each individual congener in ash sent for off-site disposal must be reported in grams.
Step 5: Calculate the quantity of dioxins/furans congeners contained in the incineration ash that was sent for off-site disposal
B.6 Calculating releases using mass balance
An electroplating facility operates a vapour degreaser. Suppose that 14 tonnes of trichloroethylene are used as a degreasing agent. Spent solvent and sludge that accumulate on the bottom of the degreaser are collected in drums for shipment to an off-site solvent reclaimer. Thirteen drums of solvent were sent to the reclaimer during the past year.
A known volume of a representative sample taken from the drums is weighed, allowed to evaporate, and reweighed. From this, it is determined that the density of the sludge is 1.03 kg/L and that the trichloroethylene concentration in the sludge shipped to the reclaimer is 30%.
Step 1: The entire 14 tonnes of solvent is released from the facility either as an air emission or as a transfer in the sludge. If the quantity of spent solvent shipped to the reclaimer is known, then the quantity transferred can be calculated based on the volume of sludge and the density of the sludge as shown below:
Step 2: The quantity of trichloroethylene emitted to air can then be calculated by mass balance by subtracting the quantity shipped in sludge to the reclaimer from the quantity purchased:
Note: trichloroethylene is a VOC and the quantity released to air in this example would also require that a report for total VOCs under Part 4 be submitted.
B.7 Calculating releases using emission factors
A facility operated a cement kiln and process throughput amounted to 2,500,000 tonnes of clinker produced during the year. In this example, the facility uses the emission factors provided in the WebFIRE database, to calculate the quantities of the individual PAHs that were incidentally manufactured and released, disposed of, or transferred for recycling. For a throughput of 2,500,000 tonnes of clinker, the following quantities of individual PAHs that are released to air are shown in Table 12.
| Individual PAHs in Part 2, for which there is an emission factor | Emission factor (mg PAHs/tonne clinker produced) | Quantity (mg) | Quantity (kg) |
|---|---|---|---|
| Fluoranthene | 2.42 | 6,050,000 | 6.05 |
| Phenanthrene | 16.9 | 42,250,000 | 42.25 |
| Pyrene | 1.46 | 3,650,000 | 3.65 |
| Total | N/A | N/A | 51.95 |
The quantity of the individual PAHs resulting from incidental manufacture totaled more than 50 kg, so the facility has met the reporting threshold for PAHs, and must report those substances which have met the 5 kg threshold.
The facility must submit a substance report to the NPRI for two of the PAHs for which there are data. The substance reports and quantity reported for on-site releases to air are: 6.05 kg of fluoranthene, and 42.25 kg of phenanthrene. No report is required for pyrene because it did not meet the 5 kg threshold. No report is required for the individual PAHs for which there are no emission factors [e.g., benz(a)anthracene]. The releases are not reported under the listing "PAHs, total unspeciated (NA - P/H)" because the facility has information for some of the individual Part 2 PAHs.
There were no releases to water or land of any incidentally manufactured PAHs, so the facility reports no releases to these media.
There is no knowledge of the quantity of incidentally manufactured PAHs in the residue from the pollution control devices (e.g., electrostatic precipitator), so the facility reports no disposals of the three PAHs.
Note: In cases where multiple process streams are present, but information on individual PAH is not available for all streams, report information on the individual PAHs and report the remaining quantity under total PAHs, i.e. "PAHs, total unspeciated (NA - P/H)." Quantities reported as individual PAHs should not be included in the quantity reported for "PAHs, total unspeciated (NA - P/H)."
B.8 Calculating releases using a speciation profile
A facility that manufactures varnish is able to calculate total VOC releases of 26.71 tonnes using an emission factor. The US Environmental Protection Agency’s SPECIATE 5.1 database contains a speciation profile that can be used to estimate releases of speciated VOCs based on the total VOCs quantity. Profile number 0066, for “Varnish Manufacturing – Bodying Oil,” is based on total organic gas (TOG), which includes compounds that are not considered to be VOCs under the ECCC definition (e.g., methane and ethane). For SPECIATE profiles that are based on TOG, the TOG to VOC ratio must applied to the annual release value before applying the profile weight percentage to derive the quantity of each VOC species released:
In this example, the quantity of methyl ethyl ketone released would be calculated as:
The quantity of methyl isobutyl ketone released would be calculated as:
B.9 Calculating releases using engineering estimates
This estimation method is based on physical/chemical properties (e.g., vapour pressure) of the substance and mathematical relationships (e.g., ideal gas law). In this example, rinse water from a copper-plating unit is treated separately from other process wastewater. Sodium hydroxide is added to precipitate the copper (Cu) in the wastewater. The precipitate formed from this reaction is removed as sludge from the facility's central clarification unit. Purchasing and inventory records indicate that 0.9 tonnes of sodium hydroxide were used for precipitating copper last year. The quantity of copper precipitated represents the quantity of copper released from this source as solid waste.
Step 1: For each mole of copper (Cu) present in the rinse water, two moles of sodium hydroxide (NaOH) must be added to precipitate the copper according to the following reaction:
Scientific literature indicates that this reaction would be complete at a pH of 7.7. Sodium hydroxide is added until a pH of 8 is maintained in the reaction mixture to ensure complete precipitation. It is also known that:
Step 2: Calculate the quantity of copper released in the wastewater treatment sludge:
The ratio of NaOH to Cu by mass is calculated as follows:
Using the proportions above, the following equation can be derived:
Where A = the quantity of copper released in the wastewater.
The estimation method is valid only if the NaOH reacts only with the Cu present in the wastewater and the reaction is complete.
B.10 Calculating total reduced sulphur releases using hydrogen sulphide equivalence factors
Total reduced Sulphur (TRS) refers to a gaseous mixture of compounds containing one or more sulphur atoms in their reduced state. For the purposes of reporting to the NPRI, this grouping is restricted to the substances listed in Table 13 below. TRS must be expressed in terms of H2S equivalents, and H2S equivalence factors are shown in Table 14.
It is important to remember that three of these TRS compounds – hydrogen sulphide (H2S), carbon disulphide (CS) and carbonyl sulphide (COS) – are also listed individually under Part 1A. If any one of these three substances meets the 10 tonne reporting threshold, that substance must also be reported individually.
| Substance name | Chemical formula | CAS RN |
|---|---|---|
| Hydrogen sulphide | H2S | 7783-06-4 |
| Carbon disulphide | CS2 | 75-15-0 |
| Carbonyl sulphide | COS | 463-58-1 |
| Dimethyl sulphide | C2H6S | 75-18-3 |
| Methyl mercaptan | CH4S | 74-93-1 |
| Dimethyl disulphide | C2H6S2 | 624-92-0 |
To use the equivalence factor method to calculate TRS, each TRS compound is converted into the H2S equivalent. The equivalent amounts are then summed and compared to the 10 tonnes MPO threshold. If the threshold is met or exceeded, a TRS substance report is required.
Table 14 illustrates how to calculate TRS using the equivalence factor method, when quantities of each of the six TRS substances are available. To calculate the amounts expressed as H2S, add the quantities of the substances multiplied by the H2S applicable equivalence factors:
| Substance name | Quantity (tonnes) | H2S equivalence factor | H2S equivalent (tonnes) |
|---|---|---|---|
| Hydrogen sulphide | 3 | 1 | 3 |
| Carbon disulphide | 2 | 0.895 | 1.79 |
| Carbonyl sulphide | 22 | 0.567 | 12.481 |
| Dimethyl sulphide | 4 | 0.548 | 2.194 |
| Methyl mercaptan | 2 | 0.708 | 1.417 |
| Dimethyl disulphide | 6 | 0.724 | 4.341 |
B.11 Converting CAC releases from ppm (volume) to tonnes
Stack test results for NOx (expressed as NO2), CO, or SO2 are usually in units of parts per million volume or ppm (volume). Before these numbers can be used to estimate releases of these substances for the NPRI they need to be converted from ppm (volume) to a mass release in tonnes.
Step 1: Calculate the stack's volumetric gas flow rate (V̇):
Step 2: Correct the stack gas flow rate for the moisture content and standard conditions:
Example: If the stack gas volumetric flow is 1,330 m3/min at 80°C and 1 atm pressure with a moisture content of 10%, the dry volumetric stack flow rate is:
Step 3: Convert from ppm (volume) to mass emission rate (kg/h):
Example: NOx is emitted from a stack that is 2.1 ppm by volume. The dry volumetric stack flow rate is 925.84 m3/min. The density of air at standard conditions is 1.29 kg/m3.
Step 4: Use the mass emission rate to calculate the yearly NOx release.
B.12 Converting CAC releases from ppm (mass) to tonnes
Stack test results for total particulate matter (TPM), PM10 or PM2.5 are usually in units of parts per million mass or ppm (mass). Before these numbers can be used to estimate releases of these substances for the NPRI, they need to be converted from ppm (mass) to a mass release in tonnes.
Step 1: Convert from ppm (mass) to the mass emission rate by converting ppm to grams/tonne and using the stack mass flow rate (kg/min) to convert to mass emission rate.
Example: The TPM emission rate from the stack is 250 ppm (mass). The dry mass flow rate is 10.54 kg/min. The stack is operational 24 hours a day, 365 days a year, i.e., 525,600 minutes per year.
Step 2: Using stack dry mass flow rate, calculate the mass emission rate
Step 3: Use the mass emission rate to calculate the yearly TPM release
B.13 Converting CAC releases from mass per volume to tonnes
Stack test results for volatile organic compounds (VOCs) are usually in units of mass per volume, e.g., µg/m3. These numbers need to be converted to an annual mass release in tonnes.
Step 1: Calculate the stack's volumetric gas flow rate (V̇):
Step 2: Correct the stack gas flow rate for the moisture content and standard conditions:
Example: If the stack gas volumetric flow is 1,330 m3/min at 80°C and 1 atm pressure with a moisture content of 10%, the dry volumetric stack flow rate is:
Step 3: Use the stack flow rate (m3/min) to convert to a mass emission rate.
Example: VOCs are emitted from a stack at a rate of 60 µg/m3. The dry volumetric stack flow rate is 925.84 m3/min:
Step 4: Use the mass emission rate to calculate the yearly VOCs release
B.14 Calculating CAC releases from source testing and fuel consumption data
Many facilities participating in a stack testing program will have information on the fuel feed rate during the test period and total annual fuel consumption. This data can be used to more accurately estimate CAC releases taking into account the process variations and production rates. For example, this method may be used if the equipment is only operational for part of the year or the fuel feed rate fluctuates based on the facility's production rate.
To illustrate this method the data in from the example in section B.12 was assigned to a boiler burning bituminous coal.
Step 1: Convert from ppm (mass) to the mass emission rate and, using the stack dry mass flow rate, calculate the mass emission rate, then convert to grams per hour (see section B.12). This results in a mass emission rate of 158.1 g/hr.
Step 2: Use the mass emission rate and the boiler fuel feed rate to create CAC production rate to fuel consumption to create an emission factor
Example: The TPM emissions being released from the stack are the result of combustion in a bituminous coal fired boiler. The stack testing results were based on a one-hour test period. The fuel feed rate of the boiler during the test was 25 kg bituminous coal per hour.
Step 3: Use the emission factor calculated above along with the boiler's specific total annual consumption of bituminous coal.
Example: The boiler in question burned 218.85 tonnes of bituminous coal in the reporting year. The calculated emission factor for TPM for this boiler was 6.324 kg per tonne bituminous coal burned.
B.15 Calculating CAC releases from source testing and total production data
Another method that can be used to estimate CAC releases is to correlate stack testing data with the facility's production data. Most facilities participating in a stack testing program will have information on the production rate during the test period and total annual production. This data can be used to more accurately estimate CAC releases, taking into account the process variations and production rates. For example, this method can be used if the process line is only operational for part of the year or the production rate fluctuates with demand for the product.
To illustrate this method, the data from the example in section B.13 was assigned to the fluidized bed prilling process used in urea production.
Step 1: Calculate the stack's volumetric gas flow rate (V̇) and correct the stack gas flow rate for the moisture content and standard conditions (see section B.13). This results in a dry stack volumetric gas flow rate of 925.84 m3/min.
Step 2: Use the stack flow rate (m3/min) to convert to a mass emission rate.
Example: VOCs are emitted from a stack at a rate of 60 µg/m3. The dry volumetric stack flow rate is 925.84 m3/min.
Step 3: Use the mass emission rate and the facility's production rate to create an emission factor for CAC releases to total production
The facility's production rate can be in tonnes product produced, number of units produced or any other applicable measure of production. Likewise, the CAC release could be in any units of mass. This example will use tonnes product produced and grams of substance released to illustrate the process.
Example: The VOC emissions being released from the stack are the result of the fluidized bed prilling processes used in urea production. The stack testing results were based on a one-hour test period. The production rate of the facility during the test was 23 tonnes of urea per hour.
Step 4: Use the emission factor calculated above along with the facility's total annual production of urea.
Example: The facility in question produces a total of 203,210 tonnes of urea in the reporting year. The emission factor, calculated above, for VOCs from the fluidized bed prilling process, was 0.145 g per tonne urea produced.
| Convert from | Convert to | Multiply by |
|---|---|---|
| pounds (lb) | kilograms (kg) | 0.453592 |
| ton (short ton) | tonnes | 0.907185 |
| foot (ft) | metre (m) | 0.304804 |
| gallon (U.S. gal) | litres (L) | 3.785412 |
| cubic foot (ft3) | cubic metre (m3) | 0.0283168 |
| Convert from | Convert to | Multiply by |
|---|---|---|
| million BTUs/hour | kilowatts (kW) | 293.1 |
| million BTUs/hour | Horsepower (Hp) | 393 |
| million BTUs | kilojoules (kJ) | 1.055 million |
| million BTUs | Gigajoules (GJ) | 1.055 |
| Convert from | Convert to | Multiply by |
|---|---|---|
| lb/1,000 gal | kg/1,000 L | 0.1198 |
| lb/ton | kg/tonne | 0.5 |
| lb/million BTUs | kg/million BTUs | 0.454 |
| lb/1,000 ton | kg/1,000 tonnes | 0.5 |
| lb/million ft3 | kg/million m3 | 16.018 |
D.1 Reporting criteria for individual stacks
CAC and speciated VOC releases to air must be assigned to individual stacks or flares when all of the following criteria are met:
- the facility-wide release threshold is met (see Table 18)
- the stack release threshold is met (see Table 18)
- the height of the stack or the effective height of the flare is ≥ 25 m or more above grade
- including the height of any building that the stack or flare is on
- The annual average exit temperature of the stack or flare is either not measured or is ≥ 50°C or more
| Substance | Substance part | Facility-wide release threshold (tonnes) | Stack release threshold (tonnes) |
|---|---|---|---|
| Carbon monoxide | Part 4 | 20 | 10 |
| Nitrogen oxides (expressed as nitrogen dioxide) | Part 4 | 20 | 20 |
| Sulphur dioxide | Part 4 | 20 | 25 |
| Total particulate matter | Part 4 | 20 | 25 |
| Particulate matter ≤ 10 micrometres (PM10) | Part 4 | 0.5 | 0.5 |
| Particulate matter ≤ 2.5 micrometres (PM2.5) | Part 4 | 0.3 | 0.25 |
| Volatile organic compounds (total) | Part 4 | 10 | 5 |
| Speciated VOCs | Part 5 | 1Footnote 8 | 0.25 |
Note that the threshold for the average annual exit temperature can only be applied if the exit temperature is determined through measurement. Estimations, values supplied by manufacturers, values used for the purposes of obtaining an operating approval or permit and default values cannot be used to compare to the temperature threshold.
D.2 Reporting releases of criteria air contaminants from individual stacks
If the reporting criteria are met for a stack or flare, releases to air of that CAC must be assigned to that stack or flare.
Case 1 facilities must report all releases from all sources. Case 2 facilities should only report releases from stationary combustion equipment.
D.2.1 Releases from specified sources
Quantities of CACs released from each stack that meets the criteria must be reported separately for each of the following categories, defined below:
- stationary fuel combustion for energy purposes
- combustion of fuels for non-energy purposes
- flaring
- use of fuels for non-energy products
- releases from all other sources not included in the above categories
Where possible, in instances where industrial process emissions are produced in combination with emissions from fuel combusted to supply energy, the emissions are to be calculated and reported separately. In cases where it is not possible to calculate emissions separately, co-mingled emissions would be reported based on the primary purpose of the unit of operation. Facilities must provide a detailed comment to explain that combined emissions are being reported, including an estimate of the percentage contribution of each category where possible.
Stationary fuel combustion for energy purposes
Stationary fuel combustion emissions: emissions resulting from the oxidation of solid, liquid, and gaseous fuels from stationary fuel combustion sources for the purpose of producing heat or work (electricity and thermal and mechanical energy).
Stationary fuel combustion sources: stationary devices that combust either a mix of or a specific type of solid, liquid, gaseous and waste fuels for the purpose of producing heat or work (electricity, and thermal and mechanical energy). This includes:
- boilers
- electricity generating units
- cogeneration units
- combustion turbines
- engines
- incinerators with heat capture and use
- heaters
- kilns
- furnaces
- burners
- ovens (including coke ovens)
- dryers
- any other stationary combustion devices
Note that flares are not considered stationary fuel combustion sources.
Combustion of fuels for non-energy purposes
Releases resulting from the oxidation of a fuel not for generating heat or work, for example, when the fuel is used as a reductant. When a fuel is used as both reductant and fuel in a process, the corresponding release would be considered for non-energy purposes; examples include blast furnaces in iron and steel plants, and smelting of base metals. Incineration without energy recovery falls into this category.
Flaring
Flaring emissions: releases resulting from the controlled combustion of a gas or liquid stream produced at the facility, the purpose of which is not to produce useful heat or work. This includes releases from:
- waste petroleum incineration
- hazardous emission prevention systems (in pilot or active mode)
- well testing
- natural gas gathering systems
- natural gas processing plant operations
- crude oil production
- pipeline operations
- petroleum refining
- chemical fertilizer production
- steel production
Use of fuels for non-energy products
Releases resulting from the use of a fuel as an input to a chemical reaction to produce a non-energy product, such as the production of hydrogen (in stand-alone hydrogen plants only), ammonia or ethylene.
Releases from all other sources not included in the above categories
Any other activities that generate stack releases that are not covered under one of the above categories. This applies to Case 1 facilities only, which must report for all sources of emissions if thresholds are met. Case 2 facilities are only required to report combustion emissions under one or more of the categories above.
D.2.2 Fuel type(s)
Where a release quantity is reported for a stack under any of the first four source categories described above, the type(s) of fuel associated with the releases must also be reported. For the purposes of reporting to the NPRI, fuels are categorized as follows:
- solid fossil fuels
- liquid fossil fuels – refined petroleum products
- gaseous fossil fuels
- natural gas liquids
- industrial production by-products used as fuel
- biomass/biofuels
- waste materials
- other fuels
Definitions of each of the fuel types are provided in the following sections.
Solid fossil fuels
- Coal
- A sedimentary deposit composed predominantly of carbon which has a composition (including inherent moisture) consisting of more than 50% by weight and more than 70% by volume of carbonaceous material. Coal is formed from plant remains that have been compacted, hardened, chemically altered, and metamorphosed by heat and pressure over geologic time. The four types of coal are generally considered to be anthracite, bituminous, sub-bituminous and lignite.
- Petroleum coke
- A black solid residue, obtained mainly by cracking and carbonizing of petroleum derived feedstocks, vacuum bottoms, tar and pitches in processes such as delayed coking or fluid coking. It consists mainly of carbon (90-95%), has low ash content, and may be used as a feedstock in coke ovens.
- Coke (from metallurgical coal)
- Solid carbonaceous residue derived from low-ash, low-sulphur bituminous coal from which the volatile constituents are driven off by baking in an oxygen free atmosphere (in coke ovens) at high temperatures so that the fixed carbon and residual ash are fused together.
- Coke breeze
- Fine sizes of crushed coke that will usually pass through a 1-2 cm screen opening and which is commonly used to produce iron ore pellets.
Liquid fossil fuels – refined petroleum products
- Heavy fuel oil (HFO)
-
A mixture of hydrocarbons composed of residual fractions from crude oil distillation and processing, characterized by its black colour, high specific gravity and high viscosity. HFO is usually composed of carbon (86% wt.), hydrogen (11% wt.) and sulphur, however it also contains impurities such as ash, metals and water. HFO is sometimes referred to as bunker fuel, or residual fuel oil. Within Canada there are three main categories of HFO:
- Type 4 is an industrial type of fuel intended primarily for burner installations not equipped with preheating facilities (viscosity of 15 centistokes at 40°C)
- Type 5 is a residual type of oil for burner installations equipped with preheating facilities requiring an oil with lower viscosity than Type 6 (viscosity of 50 centistokes at 40°C)
- Type 6 is a high-viscosity residual oil (360 centistokes at 40°C) for use in burner installations equipped with preheating facilities adequate for handling oil of high viscosity
In Canada, HFO must meet the requirements of the National Standard of Canada CAN/CGSB-3.2-2020.
- Light fuel oil (LFO)
- A crude oil distillate, light in colour, composed mostly of carbon (86% wt.), hydrogen (13% wt.) and sulphur (0.1 to 0.2% wt.) with trace amounts of ash and sediments. Since LFO is only slightly viscous (in the range of 1.2 to 3.6 centistokes at 40°C), it can be used without preheating. There are three types of LFO, type 0, 1, and 2, which are used mostly for the generation of heat in domestic and small commercial liquid-fuel burning equipment. In Canada, LFO must meet the requirements of CAN/CGSB-3.2-2020.
- Kerosene
- A light petroleum distillate typically used in space heaters, cook stoves and water heaters and which is suitable for use as a light source when burned in wick-fed lamps. Kerosene has a maximum distillation temperature of 204°C at the 10% recovery point and a final boiling point of 300°C. In Canada, kerosene must meet the requirements of CAN/CGSB‑3.3-2019.
- Diesel fuel
- Middle distillate fuel composed of conventional hydrocarbons, synthetic hydrocarbons or mixtures of conventional and synthetic hydrocarbons that boils in the range of 130–400°C and that is intended for use as fuel in compression-ignition engines. In Canada, diesel fuel must meet the requirements of CAN/CGSB‑3.517-2020.
- Gasoline
-
A petroleum distillate, or a mixture of petroleum distillates, oxygenates or additives, that is suitable for use in a spark ignition engine and that has the following characteristics, as determined from the applicable test method listed in CAN/CGSB-3.5-2016:
- a vapour pressure of at least 35 kPa
- an antiknock index of at least 80
- a distillation temperature at which 10% of the fuel has evaporated of not less than 35°C and not greater than 70°C
- a distillation temperature at which 50% of the fuel has evaporated of not less than 60°C and not greater than 120°C
- Naphtha
-
A refined or partially refined petroleum fraction with an approximate boiling temperature between 50-204°C other than:
- aviation gasoline
- aviation turbo fuel
- gasoline
- heavy fuel oil
- kerosene
- light fuel oil
- petroleum coke
Products that might meet the definition of naphtha but are not suitable to be put into a fuel system that produces heat or energy and is not burned or flared (such as some solvents) are not included in this definition. In Canada, naphtha used as fuel must meet the requirements of CAN/CGSB-3.27-2018.
Gaseous fossil fuels
- Natural gas
- An odorless, gaseous mixture of hydrocarbons, predominantly made up of methane (CH4).
Natural gas liquids
- Propane (C3H8)
-
A straight-chain saturated aliphatic hydrocarbon extracted from natural gas or refinery gas streams which is odorless, colourless and flammable. It is gaseous at standard temperature and pressure, however can also take liquid form when kept under pressure such as when stored in a propane tank. An odorant (e.g. ethyl mercaptan) is added for leak detection. In Canada, propane used as fuel must meet the requirements of CAN/CGSB-3.14-2018.
- Butane (C4H10)
- A straight-chain or branch-chain colourless and odorless flammable hydrocarbon extracted from natural gas or refinery gas streams, which is gaseous at standard temperature and pressure, but condenses into a liquid when pressurized. The compound in which the carbon atoms are linked in a straight chain is called normal butane, or n-butane; the branched-chain form is isobutane.
- Ethane (C2H6)
- A straight-chain saturated (paraffinic) colourless, flammable hydrocarbon extracted predominantly from natural gas streams and to a lesser extent, refinery gas streams. It is gaseous at standard temperature and pressure.
- Other natural gas liquids (NGLs)
-
extracted as a mixture of hydrocarbons and other gases, are produced and separated during either natural gas processing or crude oil refining. NGLs include:
- ethane
- propane
- butane
- isobutane
- pentanes plus - a mixture of hydrocarbons which includes:
- isopentane
- normal pentane
- natural gasoline
- plant condensates
- hexane plus
Industrial production by-products used as fuel
- Coke oven gas
- A by-product gas (containing hydrogen, methane, light oil, ammonia, pitch, tar and other minerals) generated during the production of metallurgical coke in a coke oven battery, where metallurgical coal is carbonized by heating it in the absence of air at temperatures in excess of 1,000°C.
- Blast furnace gas
- A by-product gas generated in a blast furnace when iron ore is reduced through the combustion of coke to metallic (liquid) iron. It typically contains about 20-30% carbon monoxide (CO) and about 2-6% hydrogen (H2) as combustible components, and a significant amount of inert gases with about 45-60% nitrogen (N2), and 20-25% carbon dioxide (CO2).
- Basic oxygen furance gas
- During the process of steelmaking in a basic oxygen furnace, oxygen (O2) is blown in the charge mix and due to the chemical reactions taking place in the converter vessel, a large amount of (basic oxygen furnace) gas at high temperature and rich in carbon monoxide (CO) is generated.
- Spent pulping liquor
- The residual liquid collected from on-site pulping operations at chemical pulp facilities that is subsequently fired in chemical recovery furnaces at kraft and soda pulp facilities or chemical recovery combustion units at sulphite or semi-chemical pulp facilities. Spent pulping liquor is primarily made up of lignin, other wood constituents and chemicals that are by-products of the manufacture of chemical pulp.
- Refinery still gas
- Any form or mixture of gases produced in refineries during the processing of crude oil into various petroleum products through such processes as distillation, cracking, reforming, etc. The principal constituents are typically methane, ethane, ethylene, normal butane, butylene, propane, propylene, etc., although the actual composition directly depends on the type of crude oil used as feedstock.
- Hydrogen (H2)
- The lightest of all gases, occurring chiefly in combination with oxygen in water; exists also in acids, bases, alcohols, petroleum, and other hydrocarbons. Hydrogen is generated as a by-product from some industrial chemical processes such as ethylene production, chlorine and sodium hydroxide (caustic) production, methanol production from natural gas, carbon black production from natural gas and sodium chlorate production. This hydrogen is typically burned as a fuel on-site and/or, in some cases, captured and sold to third parties.
- Chemical plant fuel gases
- Any form or mixture of residual process gases generated within chemical plants (e.g. ethylene or carbon black plants) during the manufacture of chemical products, which is subsequently used as fuel in the plant.
Biomass/biofuels
- Wood and wood byproducts/residues
-
Includes wood and wood byproducts/residues generated from a wide range of activities, including but not limited to:
- wood harvested from:
- forest thinning and fuels reduction activities in managed woodlands
- urban tree trimmings
- forest-derived fuels like the tops of sawn logs, wood chips and slash
- waste residue generated when manufacturing wood-based products such as:
- lumber
- furniture
- pallets
- paper
- waste generated during construction and demolition operations
- Agricultural waste
- Use of residual agricultural waste materials such as damaged hay, straw, corn stalks, nut shells, orchard prunings, etc. for fuel, typically, although not necessarily, in pellet form.
- Peat
- A soft, crumbly, dark brown heterogeneous mixture of partly decomposed organic matter, derived mostly from plant material, that has accumulated under conditions of waterlogging, oxygen deficiency, high acidity and nutrient deficiency over a long period of time. Peat contains energy that the plants it contains created using photosynthesis.
- Biochar
- A black, highly porous, carbonaceous, lightweight, fine-grained solid substance that is made by burning organic material generally from agricultural and forestry wastes at temperatures higher than 250°C in a low- or no-oxygen atmosphere in a controlled process called pyrolysis. Gasification can also be used to produce biochar, however it produces a smaller char yield compared with pyrolysis.
- Charcoal
- A solid fuel used for heating and cooking that results from the carbonization of solid biomass, typically wood.
- Ethanol
- A liquid alcohol produced biologically from the fermentation of various sugars from carbohydrates found in agricultural crops and cellulosic residues contained in crops or wood residue. Fuel ethanol has been distilled and dehydrated to create a high-octane, water-free alcohol. Ethanol is often used as a gasoline octane enhancer and oxygenate, and is commonly blended into gasoline at varying concentrations.
- Biodiesel
- A fuel made up of mono-alkyl esters of long chain fatty acids derived entirely from biological matter (e.g. soybean, canola or other vegetable oil, recycled cooking oil, animal fats). Biodiesel is made through a chemical process called transesterification which is a reaction between the oil or animal fat with an alcohol and a catalyst resulting in two products – methyl esters (i.e. biodiesel) and glycerin. Biodiesel can be used as a pure product (B100) or a blend with petroleum-based diesel fuel (e.g., B20) and should meet the requirements of CAN/CGSB-3.524-2022.
- Glycerol (C3H8O3)
- A trivalent alcohol that is also known as glycerine, it is an organic co-product of biodiesel production. Depending upon the feedstock used during biodiesel production, glycerol may contain alcohol, water, catalyst, and a host of other organic material collectively called MONG (matter organic non-glycerol).
- Bio-oil/pyrolysis oil
- A liquid biofuel produced through pyrolysis which rapidly heats biomass (typically to 350-650°C) in an oxygen-free environment to a carefully controlled temperature and then very quickly cools the volatile products formed during the reaction to produce a dark brown water-based emulsion composed of fragments of the original hemicellulose, cellulose and lignin molecules contained in the biomass.
- Biogas
- A gas mixture composed mainly of methane (CH4) and carbon dioxide (CO2), along with water and other trace gases. Biogas results from a natural degradation process of biomass performed by a large variety of micro-organisms. Included in this category are landfill gas and sludge gas (sewage gas and gas from animal slurries) as well as other forms of biogas. The ‘bio’ aspect of biogas refers to its biological production process and renewable (biomass) origin, in opposition to ‘natural gas’ which is of fossil origin.
- Syngas
- A gas mixture composed primarily of hydrogen (H2) and carbon monoxide (CO) along with hydrocarbons from the thermochemical decomposition of organic or inorganic materials. Syngas is chemically similar to natural gas and is produced from bio-fuels, oil shale, lignite coal or landfill gas. It is also referred to as substitute natural gas or synthetic natural gas.
- Biobutanol
- A fermentation isobutyl alcohol that is derived from biomass feedstocks. It must meet ASTM international specification D7862 for butanol for blending with gasoline for use as automotive spark-ignition engine fuel.
Waste materials
- Tires
- A component that is designed to surround the rim of a vehicle’s wheel and has an actual weight of one kilogram or more. A "waste tire" is a tire that is no longer mounted on a vehicle and is no longer suitable for use as a vehicle tire due to wear, damage, or deviation from the manufacturer’s original specifications. A waste tire includes scrap tires or repairable tires, and includes various types of waste fuel products derived from tires – such as tire derived fuel or tire derived chips.
- Plastics
- A material made from linking monomers through a chemical reaction to create a polymer chain that can be molded or extruded at high heat into various solid (though sometimes flexible) forms retaining their defined shapes during their life cycle and after disposal. Plastics can include material derived from either petroleum or a biologically based polymer, such as corn or other plant sources.
- Municipal solid waste
-
Material that is composed of residential, commercial, and institutional solid waste and which is managed at waste disposal, recycling or composting sites. This definition specifically excludes:
- hazardous waste
- liquid industrial waste
- gaseous waste
- agricultural wastes
- mining wastes
- liquid effluents discharged from processing or manufacturing sites
- nuclear wastes
- auto hulks
- pathological wastes
- gravel and rocks
- Used oil and lubricants
-
A petroleum-derived, mineral-based, bio-based or synthetic product (semi-solid or liquid) including:
- engine oil
- hydraulic fluid
- transmission fluid
- gear oil
- heat transfer fluid
- other oil or fluid utilized for lubrication or heat-transfer that as a result of its use, storage or handling, is altered so that it is no longer suitable for its intended purpose but is suitable for re-refining or other permitted uses (e.g. energy recovery)
- Sewage sludge
-
Solid, semi-solid, or liquid residue which contains materials removed from municipal or domestic wastewater during secondary treatment. Sewage sludge does not include:
- ash generated in a sewage sludge incinerator
- grit and screenings generated during preliminary treatment of domestic sewage in a treatment works
- animal manure
- residue generated during treatment of animal manure
- domestic septage
- Asphalt shingles
- A small unit of prepared roofing for installation with similar units in overlapping rows, with one or more layers of felt (organic or fiberglass) impregnated and coated on both sides with asphalt and surfaced with mineral granules or an alternative surfacing material that provides protection for the asphaltic coating.
- Refuse derived fuel
- A waste fuel produced by shredding and dehydrating solid waste. It mainly consists of combustible components of municipal and industrial waste such as paper, wood and plastics. It can be sold in its processed form, or it can be compressed into pellets, bricks, or logs.
- Other wastes
- New waste products suitable for use as fuel are being identified on an on-going basis. This category includes any waste material that does not fall under the other waste types already identified and defined within the waste materials category.
Other fuels
Any other substances or materials used as fuel that does not fall under any of the categories described above.
D.3 Reporting releases of speciated VOCs from individual stacks
The total quantity of each speciated VOC must be reported for each individual stack that meets thresholds. Unlike total VOCs under Part 4, quantities of speciated VOCs do not need to be reported separately by source and the fuel type(s) associated with speciated VOC releases do not need to be reported.
Case 1 facilities must report all releases from all sources. Case 2 facilities should only report releases from stationary combustion equipment
D.4 Information on stacks and flares to be reported
D.4.1 Stack/flare identification
Stack name
Each stack/flare is required to have a name, which should be as descriptive as possible to help users of the data better understand the purpose of the stack/flare and the sources associated with it.
Latitude and longitude
The latitude and longitude of each stack/flare must be reported in decimal degrees to at least five decimal places.
Provincial or territorial identification number(s)
The provincial or territorial identification number (e.g., as specified in a provincial or territorial approval or permit) for each stack/flare must be reported, where available or applicable.
D.4.2 Stack parameters (excluding flares)
Stack parameters that are reported to the NPRI should be based on measurements or estimations made at the source or in similar installations, or on values supplied by manufacturers. Default values used for modelling and permissible maximum values should not be used. Calculations may be made, based upon specific equations, to develop representative values for the effective stack parameters (see below), however this is typically only done in the case of flares. For other (i.e., non-flare) stacks, the use of representative/effective stack parameters generally should not be the norm.
Stack height
The physical height of the stack (in metres) from ground level to the level at which emissions occur. This is also referred to as the height of the stack above grade. The physical height of the stack is determined by taking the measurement from ground level to the exit level of the stack. If a stack is located on top of a building, the height of the building must be added to the height of the stack.
Stack exit diameter
The inner physical diameter (in metres) at the exit level of the stack.
If the opening at the top of the stack is circular, stack exit diameter can be calculated as follows:
Where:
- d = diameter (m)
- A = cross-sectional area (m2)
- π = 3.1416 (approximately)
If the opening at the top of the stack is not circular, equivalent diameter and hydraulic diameter can be calculated as follows:
Where:
- deq = equivalent diameter (m)
- L = length (m)
- W = width (m)
- π = 3.1416 (approximately)
Where:
- dh = hydraulic diameter (m)
- L = length (m)
- W = width (m)
Average stack exit velocity
The annual average exit velocity (in metres/second) of the gas where it exits the stack.
If unknown, the stack exit velocity can be computed from flow rate and stack diameter for rectangular and circular stacks as follows:
Where:
- v = exit velocity (m/s)
- V̇ = volumetric flow rate (m3/s)
- A = stack area (m2)
Where:
- v = exit velocity (m/s)
- Q = flow rate (m3/s)
- π = 3.1416 (approximately)
- ds = stack exit diameter (m)
Exit temperature
The annual average temperature [in degrees Celsius (°C)] of the released gas when it exits the stack, if known. If the actual temperature is not known, the facility can report the annual average stack exit temperature that was used for the purposes of obtaining a current approval or a permit, or can indicate that the annual average exit temperature is unknown. Due to the wide variety of possible non-flare stacks, ECCC does not recommend a default exit temperature for non-flare stacks.
D.4.3 Flare parameters
The unique exhaust characteristics of flares necessitate the calculation and use of exhaust effective “pseudo-parameters” to appropriately characterize the flare, in order to ensure that the resulting plume rise and plume spread are reasonably representative. The pseudo-stack parameters that are required are:
- effective stack height
- effective stack diameter
- effective stack exit velocity
- effective stack exit temperature
It is these pseudo stack parameters that are required – not the actual dimensions of the flare (i.e., actual flare height or actual flare diameter) or conditions at the flare nozzle (i.e. flare exit velocity, flare exit temperature).
Facilities should refer to guidance that has been provided directly by their respective provincial ministry of the environment or contained in the air emissions dispersion guidance document that is available in their province, if such guidance is available. This guidance may have already been used by facilities for air dispersion modelling activities that the facility has been required to undertake in support of their operating permit. The same values should be reported to the NPRI.
In the absence of such provincial guidance, facilities can use the following Ontario Ministry of the Environment and Climate Change guidance (PDF) to determine pseudo-parameters for flares.
Effective stack height
The following equations should be used to estimate the effective stack height:
Where:
- Heff = effective stack height (m)
- includes the physical stack height plus the flame length
- assumes 45° flame tilt due to wind
- Hs = physical stack height above ground (m)
- Qn = net heat released (J/s)
- QT = total heat available from combustion (J/s)
- sensible and radiative heat available estimated based on the properties of the flared gas stream including the pilot fuel and combustible lift gas
- 𝒇 = % heat lost by radiation
- a function of the molecular weight of the flared gas stream
- flares with smoky, dark plumes lose more heat via radiation (i.e., higher value for f) than clean burning flares with no visible plumes
Ranges of molecular weights of the gas stream to be flared corresponding to a given 𝒇 value are outlined in Table 19 [Ontario Ministry of the Environment and Climate Change (OMECC), 2017]. Facilities should calculate the molecular weight of their flared gas stream, based on the documented and/or measured composition considering all potential chemical constituents (e.g., flare gas, non-inert lift or sweep gas, etc.) and then select the corresponding 𝒇 value. In the absence of sufficient documentation to verify or support the composition and calculation of the molecular weight, facilities should use an 𝒇 value of 55% in calculations.
| Molecular weight (gram/mole) | Radiative heat loss values (𝒇 values) |
|---|---|
| ≤20 | 25% |
| 21-35 | 30% |
| 36-50 | 35% |
| 51-65 | 40% |
| 66-80 | 45% |
| 81-95 | 50% |
| >95 | 55% |
Effective stack diameter
If province-specific guidance is not available, the following equation should be used to estimate the effective stack diameter (OMECC, 2017):
Where:
- deff = effective diameter at the flame tip (m)
- Fb,actual = buoyancy flux (m4/s3)
- Tstack = combusted gas temperature (K) [Ontario assumes 1273 K]
- g = acceleration due to gravity (9.81 m/s2)
- veff = effective velocity at the flame tip (m/s) [minimum value = 1.5 m/s]
- Tamb = ambient temperature (K)
Effective stack exit velocity
If province-specific guidance is not available, the following equation should be used to estimate the effective stack diameter (OMECC, 2017):
Where:
- veff = effective velocity at the flame tip (m/s)
- g = acceleration due to gravity (9.81 m/s2)
- Fm = momentum flux (m4/s2)
- Fb = buoyancy flux (m4/s3)
- Tstack = combusted gas temperature (K) [Ontario assumes 1273 K]
- Tamb = ambient temperature (K)
Where:
- Fm = momentum flux (m4/s2)
- ρgas = density of gas to be flared (kg/m3)
- ρair = density of ambient air (kg/m3)
- dnozzle = flare nozzle diameter (m)
- vnozzle = actual gas exit velocity (including lift gas) at flare nozzle before combustion (m/s)
Where:
- Fb = buoyancy flux (m4/s3)
- g = acceleration due to gravity (9.81 m/s2)
- Qn = net heat release rate (J/s)
- ρair = density of air at ambient temperature and pressure (kg/m3)
- Tamb = ambient temperature (K)
- Cp,air = specific heat of dry air constant at Tamb (J/kg-K)
If information is not available to a facility to undertake the above calculations, then a default value of 20 m/s should be used.
Effective stack exit temperature
The annual average temperature [in degrees Celsius (°C)] of the released gas when it exits the stack. If the actual temperature is not known, the facility can report the annual average stack exit temperature that was used for the purposes of obtaining a current approval or a permit, or a default value of 1,000°C can be used, or the facility can indicate that the annual average exit temperature is unknown.
D.5 Exemptions from individual stack reporting requirements
D.5.1 Exemptions for certain types of facilities
Certain facilities in the oil and gas extraction except oil sands sector (NAICS code 211110) with fewer than ten employees are exempt from individual stack reporting requirements (“Case 3” and “Case 4” facilities). Releases from stacks and flares at these facilities still need to be reported, just not at the individual stack level.
D.5.2 Exemptions for certain sources
Stacks and vents from storage tanks that emit releases at or near ambient temperatures are exempt from individual stack reporting requirements. Releases from these tanks still need to be reported, just not at the individual stack level.
D.5.3 Exemptions based on stack characteristics
The following types of stacks are exempted from individual stack reporting requirements: horizontal or non-vertical stacks (e.g., gooseneck shape), and vertical stacks with rain caps. Releases from these stacks must still be reported as part of stack or point releases, but do not need to be reported separately at the individual stack level.
D.6 Stack grouping
Similar stacks can be reported as a group instead of individually, if certain conditions are met. If a facility has received prior permission from a regulatory authority to group stacks for air dispersion modelling for the purposes of obtaining approval or a permit (e.g., Ontario’s Environmental Compliance Approval), then the facility is allowed to report for those stacks as a group to the NPRI. If no prior permission has been obtained, ECCC will allow reporting of more than one stack as a group, provided the following conditions are met:
- the grouped stacks are ≥25 m and <50 m in height
- stacks ≥50 m in height cannot be grouped and will continue to be reported individually
- the grouped stacks must be within 250 m of the approximate geographic centre of the group
- releases from the grouped stacks must be ±35% of the average releases from all stacks in the group
- the stack height, inside diameter, exit temperature and exit velocity must be within ±35% of the average
- total releases from the grouped “stack” are greater than or equal to the stack air release threshold
When reporting for a grouped or virtual stack:
- the stack name needs to include the word “group” and the number of stacks included in the group
- the average height, inside diameter, and exit temperature and velocity need to be reported for the group
- the geographic coordinates of the approximate centre of the group must be reported
- a list of the stacks in each group, and information on their characteristics, provincial identification numbers and latitude and longitude need to be provided to ECCC (by email to inrp-npri@ec.gc.ca)
- total releases from each grouped “stack” would be reported through the reporting software or bulk upload
Appendix E - supplemental information on volatile organic compounds
Table 20 shows the substances that are listed in Part 5, along with the synonyms and common names of those substances, where applicable. Where more than one CAS RN applies, Table 20 also lists the names and CAS RNs that must be reported. These CAS RNs are for information only and do not necessarily include all the CAS RNs that may apply to the group or mixture. Also note that isomers of the listed substances may exist in mixtures of isomers, and the CAS RNs of these mixtures of isomers may not necessarily be listed in Table 20.
| Substance name | CAS RNFootnote 9 or NPRI substance identifierFootnote 10 | Synonym(s) | Substances that must be reported |
|---|---|---|---|
| Acetylene | 74-86-2 | Ethyne | Acetylene (CAS 74-86-2) |
| Analytically unresolved hydrocarbons (C10 to C16+) | NA – 44 | Unresolved hydrocarbons (URHCs) | Analytically unresolved hydrocarbons (C10 to C16+) (various CAS) |
| Benzene | 71-43-2 | Cyclohexatriene, phenyl hydride | Benzene (CAS 71-43-2) |
| 1,3-Butadiene | 106-99-0 | Vinyl ethylene, biethylene, bivinyl | 1,3-Butadiene (CAS 106-99-0) |
| Butane (all isomers) | NA - 24 | C4 paraffins, C4 alkanes |
|
| Butene (all isomers) | 25167-67-3 | C4 olefin, C4 alkenes, butylene |
|
| 2-Butoxyethanol | 111-76-2 | Butyl cellosolve, n-butoxyethanol, EGBE | 2-Butoxyethanol (CAS 111-76-2) |
| Butyl acetate (all isomers, exlcuding tert-butyl acetate) | NA - 41 | Acetic acid, n-butyl ester, 1-acetoxybutane, 1-butyl acetate |
|
| Cycloheptane (all isomers) | NA - 25 | C7 cycloparaffins, C7 cycloalkanes, C2 cyclopentane |
|
| Cyclohexene (all isomers) | NA - 26 | C6 cycloalkenes |
|
| Cyclooctane (all isomers) | NA - 27 | C8 cycloparaffins, C8 cycloalkanes, C2 cyclohexane |
|
| Decane (all isomers) | NA - 28 | C10 paraffins, C10 alkanes |
|
| p-Dichlorobenzene | 106-46-7 | 1,4-Dichlorobenzene, p-chlorophenyl chloride, PDCB | p-Dichlorobenzene (CAS 106-46-7) |
| 1,2-Dichloroethane | 107-06-2 | Ethylene dichloride, Freon 150 | 1,2-Dichloroethane (CAS 107-06-2) |
| Dimethylether | 115-10-6 | Methyl ether, methoxymethane | Dimethylether (CAS 115-10-6) |
| Ethanol | 64-17-5 | Ethyl alcohol, ethyl hydroxide, methylcarbinol | Ethanol (CAS 64-17-5) |
| Ethyl acetate | 141-78-6 | Ethyl acetic ester, acetoxyethane | Ethyl acetate (CAS 141-78-6) |
| Ethylene | 74-85-1 | Ethene | Ethylene (CAS 74-85-1) |
| Ethyltoluene (all isomers) | NA - 42 | o-Ethyltoluene, o-methylethylbenzene, m-ethyltoluene, p-ethylmethylbenzene, p-ethyltoluene |
|
| Formaldehyde | 50-00-0 | Methyl aldehyde, methylene glycol, oxomethane | Formaldehyde (CAS 50-00-0) |
| Furfuryl alcohol | 98-00-0 | 2-Furancarbinol, furanol, 2-furanmethanol | Furfuryl alcohol (CAS 98-00-0) |
| Heavy aromatic solvent naphtha | 64742-94-5 | Solvent naphtha (petroleum), heavy aromatic, heavy aromatic naphtha, high-flash aromatic naphtha | Heavy aromatic solvent naphtha (CAS 64742-94-5) |
| Heptane (all isomers) | NA - 31 | C7 paraffins, C7 alkanes, isomers of heptane |
|
| n-Hexane | 110-54-3 | Normal hexane, dipropyl, hexyl hydride | n-Hexane (CAS 110-54-3) |
| Hexane (all isomers, excluding n-hexane) | NA - 32 | C6 paraffins, C6 alkanes |
|
| Hexene (all isomers) | 25264-93-1 | C6 olefins, C6 alkenes |
|
| Hydrotreated heavy naphtha | 64742-48-9 | Naphtha (petroleum), hydrotreated heavy, hydrotreated light steam cracked naphtha residuum (petroleum), low boiling point hydrogen treated naphtha | Hydrotreated heavy naphtha (CAS 64742-48-9) |
| Hydrotreated light distillate | 64742-47-8 | Hydrotreated kerosene, distillate fuel oils, light, distillates (petroleum), hydrotreated light | Hydrotreated light distillate (CAS 64742-47-8) |
| Isopropyl alcohol | 67-63-0 | 2-Propanol, isopropanol, rubbing alcohol | Isopropyl alcohol (CAS 67-63-0) |
| Light aromatic solvent naphtha | 64742-95-6 | Aromatic naphtha, type 1, high flash aromatic naphtha (HFAN) | Light aromatic solvent naphtha (CAS 64742-95-6) |
| D-Limonene | 5989-27-5 | D-1,8-p-Menthadiene | D-Limonene (CAS 5989-27-5) |
| Methanol | 67-56-1 | Methyl alcohol, wood alcohol, monohydroxymethane | Methanol (CAS 67-56-1) |
| Methyl ethyl ketone | 78-93-3 | 2-Butanone, methyl acetone | Methyl ethyl ketone (CAS 78-93-3) |
| Methyl isobutyl ketone | 108-10-1 | Hexanone, isopropylacetone | Methyl isobutyl ketone (CAS 108-10-1) |
| Methylcyclopentane | 96-37-7 | Methyl cyclopentane, methylpentamethylene | Methylcyclopentane (CAS 96-37-7) |
| Mineral spirits | 64475-85-0 | N/A | Mineral spirits (CAS 64475-85-0) |
| Myrcene | 123-35-3 | 7-Methyl-3-methylene-octadiene | Myrcene (CAS 123-35-3) |
| Naphtha | 8030-30-6 | Benzine, light ligroin, petroleum distillates (naphtha), rubber solvent (naphtha) | Naphtha (CAS 8030-30-6) |
| Nonane (all isomers) | NA - 33 | C9 paraffins, C9 alkanes |
|
| Octane (all isomers) | NA - 34 | C8 paraffins, C8 alkanes |
|
| Other glycol ethers and acetates (limited to 18 substances and their isomers) | NA - 45 | N/A |
|
| Pentane (all isomers) | NA - 35 | C5 paraffins, C5 alkanes |
|
| Pentene (all isomers) | NA - 36 | C5 olefin, C5 alkenes, amylene |
|
| beta-Phellandrene | 555-10-2 | 1(7)-2-p-Menthadiene | beta-Phellandrene (CAS 555-10-2) |
| alpha-Pinene | 80-56-8 | Cyclic dexadiene | alpha-Pinene (CAS 80-56-8) |
| beta-Pinene | 127-91-3 | Nopinene | beta-Pinene (CAS 127-91-3) |
| Propane | 74-98-6 | Dimethylmethane, liquefied propane, propyl hydride | Propane (CAS 74-98-6) |
| Propyl acetate (all isomers) | NA - 43 | 1-Acetoxypropane, 2-acetoxypropane, propyl ethanoate |
|
| n-Propyl alcohol | 71-23-8 | 1-Propanol, 1-propyl alcohol | n-Propyl alcohol (CAS 71-23-8) |
| Propylene | 115-07-1 | Propene | Propylene (CAS 115-07-1) |
| Propylene glycol methyl ether acetate (PGMEA; all isomers) | 108-65-6 | Propylene glycol monomethyl ether acetate, acetic acid, 2-methoxy-1-methyl ethyl ester, 1-methoxy-2-acetoxypropane |
|
| Solvent naphtha light aliphatic | 64742-89-8 | Solvent naphtha (petroleum), light aliphatic, light aliphatic solvent naphtha, light aliphatic solvent naphtha (petroleum) | Solvent naphtha light aliphatic (CAS 64742-89-8) |
| Solvent naphtha medium aliphatic | 64742-88-7 | Solvent naphtha (petroleum), medium aliphatic, medium aliphatic solvent naphtha, medium aliphatic solvent naphtha (petroleum) | Solvent naphtha medium aliphatic (CAS 64742-88-7) |
| Stoddard solvent | 8052-41-3 | White spirits, high flash naphtha, safety solvent naphtha | Stoddard solvent (CAS 8052-41-3) |
| Styrene | 100-42-5 | Phenylethylene, vinyl benzene | Styrene (CAS 100-42-5) |
| Tetrahydrofuran | 109-99-9 | Butylene oxide, cyclotetramethylene oxide, diethylene oxide | Tetrahydrofuran (CAS 109-99-9) |
| Toluene | 108-88-3 | Methylbenzene, phenyl methane | Toluene (CAS 108-88-3) |
| 1,2,4-Trimethylbenzene | 95-63-6 | Pseudocumene | 1,2,4-Trimethylbenzene (CAS 95-63-6) |
| Trimethylbenzene (all isomers, excluding 1,2,4-trimethylbenzene) | 25551-13-7 | N/A |
|
| Vinyl acetate | 108-05-4 | Acetic acid ethylene ether | Vinyl acetate (CAS 108-05-4) |
| VM & P naphtha | 8032-32-4 | Ligroine | VM & P naphtha (CAS 8032-32-4) |
| Xylene (all isomers) | 1330-20-7 | N/A |
|
Appendix F - Individual CAS RNs of new substance groupings added to Part 1B of the NPRI substance list for 2025-2027
| CAS RN | Substance Name |
|---|---|
| 149-30-4 | 2-Mercaptobenzothiazole or 2(3H)-Benzothiazolethione (MBT) |
| 95-31-8 | 2-Benzothiazolesulfenamide, N-(1,1-dimethylethyl) (TBBS) |
| 95-33-0 | 2-Benzothiazolesulfenamide, N-cyclohexyl- (CBS) |
| 120-78-5 | Benzothiazole, 2,2’-dithiobis- (MBTS) |
| 2492-26-4 | 2(3H)-Benzothiazolethione, sodium salt (SMBT) |
| 4979-32-2 | 2-Benzothiazolesulfenamide, N,N-dicyclohexyl- (DBCS) |
| 95-29-4 | 2-Benzothiazolesulfenamide, N,N-bis(1-methylethyl)- |
| 95-32-9 | Benzothiazole, 2-(4-morpholinyldithio)- |
| 102-77-2 | Morpholine, 4-(2-benzothiazolylthio)- |
| 155-04-4 | 2(3H)-Benzothiazolethione, zinc salt |
| 3741-80-8 | 2-Benzothiazolesulfenamide, N-(2-benzothiazolylthio)-N-(1,1-dimethylethyl)- |
| 7778-70-3 | 2(3H)-Benzothiazolethione, potassium salt |
| 21564-17-0 | Thiocyanic acid, (2-benzothiazolylthio)methyl ester |
| 22405-83-0 | Zinc, dichloro[2,2’-dithiobis[benzothiazole]]-, (T-4)- |
| 32510-27-3 | 2(3H)-Benzothiazolethione, copper salt |
| 38456-45-0 | 2(3H)-Benzothiazolethione, compd. with N-ethylethanamine (1:1) |
| 65605-47-2 | 2(3H)-Benzothiazolethione, compd. with N-butyl-1-butanamine (1:1) |
| 65605-48-3 | 2(3H)-Benzothiazolethione, compd. with N,N-diethylethanamine (1:1) |
| 68911-68-2 | Amines, C12-14-tert-alkyl, compds. with 2(3H)-benzothiazolethione |
| 117920-00-0 | Amines, C16-22-tert-alkyl, compds. with 2(3H)-benzothiazolethione (1:1) |
| CAS RN | Substance Name |
|---|---|
| 112-69-6 | 1-Hexadecanamine,N, N-dimethyl- |
| 124-30-1 | 1-Octadecanamine |
| 61788-46-3Footnote 11 | Amines, coco alkyl |
| 61789-79-5Footnote 11 | Amines,bis(hydrogenated tallow alkyl) |
| 61790-59-8Footnote 11 | Amines, hydrogenated tallow alkyl, acetates |
| 61790-60-1Footnote 11 | Amines, tallow alkyl, acetates |
| 61791-55-7Footnote 11 | Amines,N-tallowalkyltrimethylenedi- |
| 68479-04-9Footnote 11Footnote 12 | 1,3-Propanediamine,N-[3-(tridecyloxy)propyl]-, branched |
| 68783-25-5Footnote 11 | Amines,N,N,N’-trimethyl-N’-tallowalkyltrimethylenedi- |
| 111-86-4 | 1-Octanamine |
| 112-18-5 | 1-Dodecanamine,N,N-dimethyl- |
| 112-75-4 | 1-Tetradecanamine,N,N-dimethyl- |
| 112-90-3 | 9-Octadecen-1-amine, (Z)- |
| 112-99-2 | 1-Octadecanamine, N-octadecyl- |
| 124-22-1 | 1-Dodecanamine |
| 124-28-7 | 1-Octadecanamine,N,N-dimethyl- |
| 143-27-1 | 1-Hexadecanamine |
| 929-73-7 | 1-Dodecanamine, hydrochloride |
| 1120-24-7 | 1-Decanamine,N,N-dimethyl- |
| 1613-17-8 | 1-Octadecanamine,N,N-dimethyl-, hydrochloride |
| 1838-08-0 | 1-Octadecanamine, hydrochloride |
| 1920-05-4 | 1-Dodecanamine,N,N-dimethyl-, acetate |
| 2016-56-0 | 1-Dodecanamine, acetate |
| 2016-57-1 | 1-Decanamine |
| 2190-04-7 | 1-Octadecanamine, acetate |
| 3007-31-6 | 1-Dodecanamine, N-dodecyl- |
| 4455-26-9 | 1-Octanamine, N-methyl-N-octyl- |
| 5538-95-4 | 1,3-Propanediamine, N-dodecyl- |
| 7173-62-8 | 1,3-Propanediamine, N-9-octadecenyl-, (Z)- |
| 7378-99-6 | 1-Octanamine,N,N-dimethyl- |
| 7396-58-9 | 1-Decanamine, N-decyl-N-methyl- |
| 10460-00-1 | 9-Octadecen-1-amine, (Z)-, acetate |
| 13281-06-6 | 1,3-Propanediamine, N-(2-ethylhexyl)- |
| 14676-61-0 | 1-Propanamine, 3-(tridecyloxy)- |
| 19855-61-9 | 1-Octadecanamine,N,N-dimethyl-, acetate |
| 22020-14-0 | 1-Decanamine, N-methyl-N-octyl- |
| 22023-23-0 | 1,3-Propanediamine, N-[3-(tridecyloxy)propyl]- |
| 24287-35-2 | 1-Tetradecanamine,N,N-dimethyl-, acetate |
| 25324-14-5 | 1-Hexadecanamine,N,N-dimethyl-, acetate |
| 28061-69-0 | Octadecen-1-amine,N,N-dimethyl- |
| 28701-67-9 | 1-Propanamine, 3-(isodecyloxy)-, acetate |
| 29317-52-0 | 1-Propanamine, 3-(isononyloxy)- |
| 30113-45-2 | 1-Propanamine, 3-(isodecyloxy)- |
| 40165-68-2 | 9-Octadecen-1-amine, N-9-octadecenyl-, (Z,Z)- |
| 50291-24-2 | 1-Dodecanamine, sulfate |
| 61788-45-2 | Amines, hydrogenated tallow alkyl |
| 61788-62-3 | Amines,dicocoalkylmethyl |
| 61788-63-4 | Amines,bis(hydrogenated tallowalkyl)methyl |
| 61788-91-8 | Amines, dimethyl soya alkyl |
| 61788-93-0 | Amines, cocoalkyldimethyl |
| 61788-95-2 | Amines, (hydrogenated tallowalkyl)dimethyl |
| 61789-76-2 | Amines,dicocoalkyl |
| 61790-18-9 | Amines, soya alkyl |
| 61790-33-8 | Amines, tallow alkyl |
| 61790-57-6 | Amines, coco alkyl, acetates |
| 65059-85-0 | 1-Heptadecanamine,N,N-dimethyl-, acetate |
| 67700-98-5 | Amines, C10-16-alkyldimethyl |
| 67700-99-6 | Amines, di-C14-18-alkylmethyl |
| 68037-91-2 | Amines, C14-18-alkyl |
| 68037-92-3 | Amines, C16-22-alkyl |
| 68037-95-6 | Amines, C16-18and C18-unsatd. alkyl |
| 68037-98-9 | Amines, di-C14-18-alkyl |
| 68130-68-7 | 1,3-Propanediamine, N-[3-(C12-18-alkyloxy)propyl]derivs. |
| 68155-38-4 | Amines, C14-18and C16-18-unsatd. alkyl |
| 68439-70-3 | Amines, C12-16-alkyldimethyl |
| 68513-50-8 | 1-Tridecanamine, N-tridecyl-, branched |
| 68603-64-5 | Amines, N-(hydrogenated tallow alkyl)trimethylenedi- |
| 68603-65-6 | Amines,methylditallowalkyl |
| 68610-26-4 | 1-Propanamine, 3-(C12-15-alkyloxy)derivs. |
| 68610-68-4 | 1-Propanamine, 3-(C8-10-alkyloxy)derivs., acetates |
| 68783-23-3 | Amines,disoyaalkyl |
| 68783-24-4 | Amines,ditallowalkyl |
| 68784-38-3 | 1-Propanamine, 3-(C8-10-alkyloxy)derivs. |
| 68814-69-7 | Amines,dimethyltallowalkyl |
| 68855-63-0 | Amines, C16and C18-unsatd. alkyl |
| 68909-95-5 | 1-Propanamine, 3-(tridecyloxy)-, branched and linear |
| 68955-53-3 | Amines, C12-14-tert-alkyl |
| 68955-54-4 | Amines, C16-22-tert-alkyl |
| 71011-01-3 | Amines,bis(hydrogenated tallow alkyl), acetates |
| 71011-03-5 | Amines,ditallowalkyl, acetates |
| 75444-69-8 | Amines, C16-22-alkyldimethyl |
| 125328-36-1 | Amines, C20-22, acetates |
| 125328-37-2 | Amines, C20-22-alkyl |
| 125328-38-3 | Amines, canola-oil alkyl |
| 125328-39-4 | Amines, N-canola-oilalkyltrimethylenedi- |
| 125328-41-8 | Amines, hydrogenated canola-oil alkyl |
| 125328-42-9 | Amines, (hydrogenated canola-oilalkyl)dimethyl |
| 125328-43-0 | Amines, hydrogenated rape-oil alkyl |
| 125328-44-1 | Amines, hydrogenated rape-oil alkyl, acetates |
| 125328-45-2 | Amines, hydrogenated tallow alkyl,distn., residues |
| 125328-46-3 | Amines, rape-oil alkyl |
| 1078712-76-1 | Amines, (2-ethylhexyl)(hydrogenated tallowalkyl)methyl |
| CAS RN | Substance name | Common name(s) |
|---|---|---|
| 143-33-9 | Sodium cyanide | Sodium cyanide |
| 506-61-6 | Argentate(1-), bis(cyano-C)-, potassium | Potassium dicyanoargentate |
| 13967-50-5 | Aurate(1-), bis(cyano-C)-, potassium | Potassium dicyanoaurate |
| 13601-19-9 | Ferrate(4-), hexakis(cyano-C)-, tetrasodium, (OC-6-11) | Tetrasodium ferrocyanide (Yellow prussiate of soda) |
| 13746-66-2 | Ferrate(3-), hexakis(cyano-C)-, tripotassium, (OC-6-11)- | Tripotassium ferricyanide |
| 13943-58-3 | Ferrate(4-), hexakis(cyano-C)-, tetrapotassium, (OC-6-11)- | Tetrapotassium ferrocyanide (Yellow prussiate of potash) |
| 14038-43-8 | Ferrate(4-), hexakis(cyano-C)-, iron(3+) (3:4), (OC-6-11)- | Ferric ferrocyanide or Prussian blue, insoluble |
| 25869-00-5 | Ferrate(4-), hexakis(cyano-C)-, ammonium iron(3+) (1:1:1),(OC-6-11)- | Ferric ammonium ferrocyanide |
| 25869-98-1 | Ferrate(4-), hexakis(cyano-C)-, iron(3+) potassium (1:1:1), (OC-6-11) | Potassium ferric ferrocyanide (Turnbull's blue or Prussian blue, soluble) |