22003A0717(01)

 

Protocol to the 1979 Convention on long-range transboundary air

pollution to abate acidification, eutrophication and ground-level

ozone

 

Official Journal L 179 , 17/07/2003 P. 0003 - 0054 

 

Dates:

of document:   30/11/1999

of effect:   00/00/0000; Entry into force See Art 17

of signature:   30/11/1999; GEBORG

end of validity:   99/99/9999

 

Authentic language: English ; French ; Russian

Author:

United Nations Organisation

 

Subject matter: Environment ; External relations

Directory code: 11306000 ; 15104000 ; 15102030

EUROVOC descriptor: atmospheric pollution ; stratospheric pollution

; transfrontier pollution ; acidification ; eutrophication ; ozone ;

pollution control measures ; accession to an agreement ;

international convention ; protocol

 

Legal basis:

102E175................... Adoption

102E300-P2L1FR1........... Adoption

102E300-P3L1.............. Adoption

Instruments cited:

293A0621(01)..............

298A1203(02)..............

Amendment to:

279A1113(01)...... Amendment..... Addition PROT from DATEFF

Amended by:

Adopted by.... 303D0507..........

 

 

 

 

ANNEX

 

 

PROTOCOL TO THE 1979 CONVENTION ON LONG-RANGE TRANSBOUNDARY AIR

POLLUTION TO ABATE ACIDIFICATION, EUTROPHICATION AND GROUND-LEVEL

OZONE

 

THE PARTIES,

DETERMINED to implement the Conve ntion on Long-range Transboundary

Air Pollution,

AWARE that nitrogen oxides, sulphur, volatile organic compounds and

reduced nitrogen compounds have been associated with adverse effects

on human health and the environment,

CONCERNED that critical loads of acidification, critical loads of

nutrient nitrogen and critical levels of ozone for human health and

vegetation are still exceeded in many areas of the United Nations

Economic Commission for Europe's region,

CONCERNED ALSO that emitted nitrogen oxides, sulphur and volatile

organic compounds, as well as secondary pollutants such as ozone and

the reaction products of ammonia, are transported in the atmosphere

over long distances and may have adverse transboundary effects,

RECOGNISING that emissions from Parties within the United Nations

Economic Commission for Europe's region contribute to air pollution

on the hemispheric and global scales, and recognising the potential

for transport between continents and the need for further study with

regard to that potential,

RECOGNISING ALSO that Canada and the United States of America are

bilaterally negotiating reductions of emissions of nitrogen oxides

and volatile organic compounds to address the transboundary ozone

effect,

RECOGNISING FURTHERMORE that Canada will undertake further

reductions of emissions of sulphur by 2010 through the

implementation of the Canada-wide Acid Rain Strategy for Post-2000,

and that the United States is committed to the implementation of a

nitrogen oxides reduction programme in the eastern United States and

to the reduction in emissions necessary to meet its national ambient

air quality standards for particulate matter,

RESOLVED to apply a multi-effect, multi-pollutant approach to

preventing or minimising the excess of critical loads and levels,

TAKING INTO ACCOUNT the emissions from certain existing activities

and installations responsible for present air pollution levels and

the development of future activities and installations,

AWARE that techniques and management practices are available to

reduce emissions of these substances,

RESOLVED to take measures to anticipate, prevent or minimise

emissions of these substances, taking into account the application

of the precautionary approach as set forth in principle 15 of the

Rio Declaration on Environment and Development,

REAFFIRMING that States have, in accordance with the Charter of the

United Nations and the principles of international law, the

sovereign right to exploit their own resources pursuant to their own

environmental and developmental policies, and the responsibility to

ensure that activities within their jurisdiction or control do not

cause damage to the environment of other States or of areas beyond

the limits of national jurisdiction,

CONSCIOUS of the need for a cost-effective regional approach to

combating air pollution that takes account of the variations in

effects and abatement costs between countries,

NOTING the important contribution of the private and

non-governmental sectors to knowledge of the effects associated with

these substances and available abatement techniques, and their role

in assisting in the reduction of emissions to the atmosphere,

BEARING IN MIND that measures taken to reduce emissions of sulphur,

nitrogen oxides, ammonia and volatile organic compounds should not

constitute a means of arbitrary or unjustifiable discrimination or a

disguised restriction on international competition and trade,

TAKING INTO CONSIDERATION the best available scientific and

technical knowledge and data on emissions, atmospheric processes and

effects on human health and the environment of these substances, as

well as on abatement costs, and acknowledging the need to improve

this knowledge and to continue scientific and technical cooperation

to further understanding of these issues,

NOTING that pursuant to the Protocol concerning the Control of

Emissions of Nitrogen Oxides or their Transboundary Fluxes, adopted

at Sofia on 31 October 1988, and the Protocol concerning the Control

of Emissions of Volatile Organic Compounds or their Transboundary

Fluxes, adopted at Geneva on 18 November 1991, there is already

provision to control emissions of nitrogen oxides and volatile

organic compounds, and that the technical Annexes to both those

Protocols already contain technical guidance for reducing these

emissions,

NOTING ALSO that pursuant to the Protocol on Further Reduction of

Sulphur Emissions, adopted at Oslo on 14 June 1994, there is already

provision to reduce sulphur emissions in order to contribute to the

abatement of acid deposition by diminishing the exceedances of

critical sulphur depositions, which has been derived from critical

loads of acidity according to the contribution of oxidised sulphur

compounds to the total acid deposition in 1990,

NOTING FURTHERMORE that this Protocol is the first agreement under

the Convention to deal specifically with reduced nitrogen compounds,

BEARING IN MIND that reducing the emissions of these substances may

provide additional benefits for the control of other pollutants,

including in particular transboundary secondary particulate

aerosols, which contribute to human health effects associated with

exposure to airborne particulates,

BEARING IN MIND ALSO the need to avoid, in so far as possible,

taking measures for the achievement of the objectives of this

Protocol that aggravate other health and environment-related

problems,

NOTING that measures taken to reduce the emissions of nitrogen

oxides and ammonia should involve consideration of the full

biogeochemical nitrogen cycle and, so far as possible, not increase

emissions of reactive nitrogen including nitrous oxide which could

aggravate other nitrogen-related problems,

AWARE that methane and carbon monoxide emitted by human activities

contribute, in the presence of nitrogen oxides and volatile organic

compounds, to the formation of tropospheric ozone, and

AWARE ALSO of the commitments that Parties have assumed under the

United Nations Framework Convention on Climate Change,

HAVE AGREED AS FOLLOWS:

 

Article 1

Definitions

For the purposes of the present Protocol,

1. "Convention" means the Convention on Long-range Transboundary Air

Pollution, adopted at Geneva on 13 November 1979;

2. "EMEP" means the Cooperative Programme for Monitoring and

Evaluation of Long-range Transmission of Air Pollutants in Europe;

3. "Executive Body" means the Executive Body for the Convention

constituted under Article 10 (1) of the Convention;

4. "Commission" means the United Nations Economic Commission for

Europe;

5. "Parties" means, unless the context otherwise requires, the

Parties to the present Protocol;

6. "Geographical scope of EMEP" means the area defined in Article 1

(4) of the Protocol to the 1979 Convention on Long-range

Transboundary Air Pollution on Long-term Financing of the

Cooperative Programme for Monitoring and Evaluation of the

Long-range Transmission of Air Pollutants in Europe (EMEP), adopted

at Geneva on 28 September 1984;

7. "Emission" means the release of a substance from a point or

diffuse source into the atmosphere;

8. "Nitrogen oxides" means nitric oxide and nitrogen dioxide,

expressed as nitrogen dioxide (NO2);

9. "Reduced nitrogen compounds" means ammonia and its reaction

products;

10. "Sulphur" means all sulphur compounds, expressed as sulphur

dioxide (SO2);

11. "Volatile organic compounds", or "VOCs", means, unless otherwise

specified, all organic compounds of an anthropogenic nature, other

than methane, that are capable of producing photochemical oxidants

by reaction with nitrogen oxides in the presence of sunlight;

12. "Critical load" means a quantitative estimate of an exposure to

one or more pollutants below which significant harmful effects on

specified sensitive elements of the environment do not occur,

according to present knowledge;

13. "Critical levels" means concentrations of pollutants in the

atmosphere above which direct adverse effects on receptors, such as

human beings, plants, ecosystems or materials, may occur, according

to present knowledge;

14. "Pollutant emissions management area", or "PEMA", means an area

designated in Annex III under the conditions laid down in Article 3

(9);

15. "Stationary source" means any fixed building, structure,

facility, installation or equipment that emits or may emit sulphur,

nitrogen oxides, volatile organic compounds or ammonia directly or

indirectly into the atmosphere;

16. "New stationary source" means any stationary source of which the

construction or substantial modification is commenced after the

expiry of one year from the date of entry into force of the present

Protocol. It shall be a matter for the competent national

authorities to decide whether a modification is substantial or not,

taking into account such factors as the environmental benefits of

the modification.

 

Article 2

Objective

The objective of the present Protocol is to control and reduce

emissions of sulphur, nitrogen oxides, ammonia and volatile organic

compounds that are caused by anthropogenic activities and are likely

to cause adverse effects on human health, natural ecosystems,

materials and crops, due to acidification, eutrophication or

ground-level ozone as a result of long-range transboundary

atmospheric transport, and to ensure, as far as possible, that in

the long term and in a step-by-step approach, taking into account

advances in scientific knowledge, atmospheric depositions or

concentrations do not exceed:

(a) for Parties within the geographical scope of EMEP and Canada,

the critical loads of acidity, as described in Annex I;

(b) for Parties within the geographical scope of EMEP, the critical

loads of nutrient nitrogen, as described in Annex I;

(c) for ozone:

(i) for Parties within the geographical scope of EMEP, the critical

levels of ozone, as given in Annex I;

(ii) for Canada, the Canada-wide Standard for ozone;

(iii) for the United States of America, the National Ambient Air

Quality Standard for ozone.

 

Article 3

Basic obligations

1. Each Party having an emission ceiling in any table in Annex II

shall reduce and maintain the reduction in its annual emissions in

accordance with that ceiling and the timescales specified in that

Annex. Each Party shall, as a minimum, control its annual emissions

of polluting compounds in accordance with the obligations in Annex

II.

2. Each Party shall apply the limit values specified in Annexes IV,

V and VI to each new stationary source within a stationary source

category as identified in those Annexes, no later than the

timescales specified in Annex VII. As an alternative, a Party may

apply different emission reduction strategies that achieve

equivalent overall emission levels for all source categories

together.

3. Each Party shall, in so far as it is technically and economically

feasible and taking into consideration the costs and advantages,

apply the limit values specified in Annexes IV, V and VI to each

existing stationary source within a stationary source category as

identified in those Annexes, no later than the timescales specified

in Annex VII. As an alternative, a Party may apply different

emission reduction strategies that achieve equivalent overall

emission levels for all source categories together or, for Parties

outside the geographical scope of EMEP, that are necessary to

achieve national or regional goals for acidification abatement and

to meet national air quality standards.

4. Limit values for new and existing boilers and process heaters

with a rated thermal input exceeding 50 MWth and new heavy-duty

vehicles shall be evaluated by the Parties at a session of the

Executive Body with a view to amending Annexes IV, V and VIII no

later than two years after the date of entry into force of the

present Protocol.

5. Each Party shall apply the limit values for the fuels and new

mobile sources identified in Annex VIII, no later than the

timescales specified in Annex VII.

6. Each Party should apply the best available techniques to mobile

sources and to each new or existing stationary source, taking into

account guidance documents I to V adopted by the Executive Body at

its seventeenth session (Decision 1999/1) and any amendments

thereto.

7. Each Party shall take appropriate measures based, inter alia, on

scientific and economic criteria to reduce emissions of volatile

organic compounds associated with the use of products not included

in Annexes VI or VIII. The Parties shall, no later than at the

second session of the Executive Body after the entry into force of

the present Protocol, consider with a view to adopting an annex on

products, including criteria for the selection of such products,

limit values for the volatile organic compound content of products

not included in Annex VI or VIII, as well as timescales for the

application of the limit values.

8. Each Party shall, subject to paragraph (10):

(a) apply, as a minimum, the ammonia control measures specified in

Annex IX;

(b) apply, where it considers it appropriate, the best available

techniques for preventing and reducing ammonia emissions, as listed

in guidance document V adopted by the Executive Body at its

seventeenth session (Decision 1999/1) and any amendments thereto.

9. Paragraph (10) shall apply to any Party:

(a) whose total land area is greater than 2 million square

kilometres;

(b) whose annual emissions of sulphur, nitrogen oxides, ammonia

and/or volatile organic compounds contributing to acidification,

eutrophication or ozone formation in areas under the jurisdiction of

one or more other Parties originate predominantly from within an

area under its jurisdiction that is listed as a PEMA in Annex III,

and which has presented documentation in accordance with

subparagraph (c) to this effect;

(c) which has submitted upon signature, ratification, acceptance or

approval of, or accession to, the present Protocol a description of

the geographical scope of one or more PEMAs for one or more

pollutants, with supporting documentation, for inclusion in Annex

III;

(d) which has specified upon signature, ratification, acceptance or

approval of, or accession to, the present Protocol its intention to

act in accordance with this paragraph.

10. A Party to which this paragraph applies shall:

(a) if within the geographical scope of EMEP, be required to comply

with the provisions of this Article and Annex II only within the

relevant PEMA for each pollutant for which a PEMA within its

jurisdiction is included in Annex III; or

(b) if not within the geographical scope of EMEP, be required to

comply with the provisions of paragraphs (1), (2), (3), (5), (6) and

(7) and Annex II, only within the relevant PEMA for each pollutant

(nitrogen oxides, sulphur and/or volatile organic compounds) for

which a PEMA within its jurisdiction is included in Annex III, and

shall not be required to comply with paragraph (8) anywhere within

its jurisdiction.

11. Canada and the United States of America shall, upon their

ratification, acceptance or approval of, or accession to, the

present Protocol, submit to the Executive Body their respective

emission reduction commitments with respect to sulphur, nitrogen

oxides and volatile organic compounds for automatic incorporation

into Annex II.

12. The Parties shall, subject to the outcome of the first review

provided for under Article 10 (2), and no later than one year after

completion of that review, commence negotiations on further

obligations to reduce emissions.

 

Article 4

Exchange of information and technology

1. Each Party shall, in a manner consistent with its laws,

regulations and practices and in accordance with its obligations in

the present Protocol, create favourable conditions to facilitate the

exchange of information, technologies and techniques, with the aim

of reducing emissions of sulphur, nitrogen oxides, ammonia and

volatile organic compounds by promoting inter alia:

1. the development and updating of databases on best available

techniques, including those that increase energy efficiency,

low-emission burners and good environmental practice in agriculture;

 

2. the exchange of information and experience in the development of

less polluting transport systems;

3. direct industrial contacts and cooperation, including joint

ventures;

4. the provision of technical assistance.

2. In promoting the activities specified in paragraph (1), each

Party shall create favourable conditions for the facilitation of

contacts and cooperation among appropriate organisations and

individuals in the private and public sectors that are capable of

providing technology, design and engineering services, equipment or

finance.

 

Article 5

Public awareness

1. Each Party shall, in a manner consistent with its laws,

regulations and practices, promote the provision of information to

the general public, including information on:

(a) national annual emissions of sulphur, nitrogen oxides, ammonia

and volatile organic compounds and progress towards compliance with

the national emission ceilings or other obligations referred to in

Article 3;

(b) depositions and concentrations of the relevant pollutants and,

where applicable, these depositions and concentrations in relation

to critical loads and levels referred to in Article 2;

(c) levels of tropospheric ozone;

(d) strategies and measures applied or to be applied to reduce air

pollution problems dealt with in the present Protocol and set out in

Article 6.

2. Furthermore, each Party may make information widely available to

the public with a view to minimising emissions, including

information on:

(a) less polluting fuels, renewable energy and energy efficiency,

including their use in transport;

(b) volatile organic compounds in products, including labelling;

(c) management options for wastes containing volatile organic

compounds that are generated by the public;

(d) good agricultural practices to reduce emissions of ammonia;

(e) health and environmental effects associated with the pollutants

covered by the present Protocol;

(f) steps which individuals and industries may take to help reduce

emissions of the pollutants covered by the present Protocol.

 

Article 6

Strategies, policies, programmes, measures and information

1. Each Party shall, as necessary and on the basis of sound

scientific and economic criteria, in order to facilitate the

implementation of its obligations under Article 3:

(a) adopt supporting strategies, policies and programmes without

undue delay after the present Protocol enters into force for it;

(b) apply measures to control and reduce its emissions of sulphur,

nitrogen oxides, ammonia and volatile organic compounds;

(c) apply measures to encourage the increase of energy efficiency

and the use of renewable energy;

(d) apply measures to decrease the use of polluting fuels;

(e) develop and introduce less polluting transport systems and

promote traffic management systems to reduce overall emissions from

road traffic;

(f) apply measures to encourage the development and introduction of

low-polluting processes and products, taking into account guidance

documents I to V adopted by the Executive Body at its seventeenth

session (Decision 1999/1) and any amendments thereto;

(g) encourage the implementation of management programmes to reduce

emissions, including voluntary programmes, and the use of economic

instruments, taking into account guidance document VI adopted by the

Executive Body at its seventeenth session (Decision 1999/1) and any

amendments thereto;

(h) implement and further elaborate policies and measures in

accordance with its national circumstances, such as the progressive

reduction or phasing-out of market imperfections, fiscal incentives,

tax and duty exemptions and subsidies in all sectors that emit

sulphur, nitrogen oxides, ammonia and volatile organic compounds

which run counter to the objective of the Protocol, and apply market

instruments;

(i) apply measures, where cost-effective, to reduce emissions from

waste products containing volatile organic compounds.

2. Each Party shall collect and maintain information on:

(a) actual levels of emissions of sulphur, nitrogen compounds and

volatile organic compounds, and of ambient concentrations and

depositions of these compounds and ozone, taking into account, for

those Parties within the geographical scope of EMEP, the work plan

of EMEP;

(b) the effects of ambient concentrations and of the deposition of

sulphur, nitrogen compounds, volatile organic compounds and ozone on

human health, terrestrial and aquatic ecosystems and materials.

3. Any Party may take more stringent measures than those required by

the present Protocol.

 

Article 7

Reporting

1. Subject to its laws and regulations and in accordance with its

obligations under the present Protocol:

(a) each Party shall report, through the Executive Secretary of the

Commission, to the Executive Body, on a periodic basis as determined

by the Parties at a session of the Executive Body, information on

the measures that it has taken to implement the present Protocol.

Moreover:

(i) where a Party applies different emission-reduction strategies

under Article 3 (2) and (3), it shall document the strategies

applied and its compliance with the requirements of those

paragraphs;

(ii) where a Party judges certain limit values, as specified in

accordance with Article 3 (3), not to be technically and

economically feasible, taking into consideration the costs and

advantages, it shall report and justify this;

(b) each Party within the geographical scope of EMEP shall report,

through the Executive Secretary of the Commission, to EMEP, on a

periodic basis to be determined by the Steering Body of EMEP and

approved by the Parties at a session of the Executive Body, the

following information:

(i) levels of emissions of sulphur, nitrogen oxides, ammonia and

volatile organic compounds using, as a minimum, the methodologies

and the temporal and spatial resolution specified by the Steering

Body of EMEP;

(ii) levels of emissions of each substance in the reference year

(1990) using the same methodologies and temporal and spatial

resolution;

(iii) data on projected emissions and current reduction plans;

(iv) where it deems it appropriate, any exceptional circumstances

justifying emissions that are temporarily higher than the ceilings

established for it for one or more pollutants;

(c) parties in areas outside the geographical scope of EMEP shall

make available information similar to that specified in subparagraph

(b), if requested to do so by the Executive Body.

2. The information to be reported in accordance with paragraph

(1)(a) shall be in conformity with a decision regarding format and

content to be adopted by the Parties at a session of the Executive

Body. The terms of this decision shall be reviewed as necessary to

identify any additional elements regarding the format or the content

of the information that is to be included in the reports.

3. In good time before each annual session of the Executive Body,

EMEP shall provide information on:

(a) ambient concentrations and depositions of sulphur and nitrogen

compounds as well as, where available, ambient concentrations of

volatile organic compounds and ozone;

(b) calculations of sulphur and oxidised and reduced-nitrogen

budgets and relevant information on the long-range transport of

ozone and its precursors.

Parties in areas outside the geographical scope of EMEP shall make

available similar information if requested to do so by the Executive

Body.

4. The Executive Body shall, in accordance with Article 10 (2)(b),

of the Convention, arrange for the preparation of information on the

effects of depositions of sulphur and nitrogen compounds and

concentrations of ozone.

5. The Parties shall, at sessions of the Executive Body, arrange for

the preparation, at regular intervals, of revised information on

calculated and internationally optimised allocations of emission

reductions for the States within the geographical scope of EMEP,

using integrated assessment models, including atmospheric transport

models, with a view to reducing further, for the purposes of Article

3 (1), the difference between actual depositions of sulphur and

nitrogen compounds and critical load values as well as the

difference between actual ozone concentrations and the critical

levels of ozone specified in Annex I, or such alternative assessment

methods as approved by the Parties at a session of the Executive

Body.

 

Article 8

Research, development and monitoring

The Parties shall encourage research, development, monitoring and

cooperation related to:

(a) the international harmonisation of methods for the calculation

and assessment of the adverse effects associated with the substances

addressed by the present Protocol for use in establishing critical

loads and critical levels and, as appropriate, the elaboration of

procedures for such harmonisation;

(b) the improvement of emission databases, in particular those on

ammonia and volatile organic compounds;

(c) the improvement of monitoring techniques and systems and of the

modelling of transport, concentrations and depositions of sulphur,

nitrogen compounds and volatile organic compounds, as well as of the

formation of ozone and secondary particulate matter;

(d) the improvement of the scientific understanding of the long-term

fate of emissions and their impact on the hemispheric background

concentrations of sulphur, nitrogen, volatile organic compounds,

ozone and particulate matter, focusing, in particular, on the

chemistry of the free troposphere and the potential for

intercontinental flow of pollutants;

(e) the further elaboration of an overall strategy to reduce the

adverse effects of acidification, eutrophication and photochemical

pollution, including synergisms and combined effects;

(f) strategies for the further reduction of emissions of sulphur,

nitrogen oxides, ammonia and volatile organic compounds based on

critical loads and critical levels as well as on technical

developments, and the improvement of integrated assessment modelling

to calculate internationally optimised allocations of emission

reductions taking into account the need to avoid excessive costs for

any Party. Special emphasis should be given to emissions from

agriculture and transport;

(g) the identification of trends over time and the scientific

understanding of the wider effects of sulphur, nitrogen and volatile

organic compounds and photochemical pollution on human health,

including their contribution to concentrations of particulate

matter, the environment, in particular acidification and

eutrophication, and materials, especially historic and cultural

monuments, taking into account the relationship between sulphur

oxides, nitrogen oxides, ammonia, volatile organic compounds and

tropospheric ozone;

(h) emission abatement technologies, and technologies and techniques

to improve energy efficiency, energy conservation and the use of

renewable energy;

(i) the efficacy of ammonia control techniques for farms and their

impact on local and regional deposition;

(j) the management of transport demand and the development and

promotion of less polluting modes of transport;

(k) the quantification and, where possible, economic evaluation of

benefits for the environment and human health resulting from the

reduction of emissions of sulphur, nitrogen oxides, ammonia and

volatile organic compounds;

(l) the development of tools for making the methods and results of

this work widely applicable and available.

 

Article 9

Compliance

Compliance by each Party with its obligations under the present

Protocol shall be reviewed regularly. The Implementation Committee

established by Decision 1997/2 of the Executive Body at its

fifteenth session shall carry out such reviews and report to the

Parties at a session of the Executive Body in accordance with the

terms of the Annex to that Decision, including any amendments

thereto.

 

Article 10

Reviews by the Parties at sessions of the Executive Body

1. The Parties shall, at sessions of the Executive Body, pursuant to

Article 10 (2)(a), of the Convention, review the information

supplied by the Parties, EMEP and subsidiary bodies of the Executive

Body, the data on the effects of concentrations and depositions of

sulphur and nitrogen compounds and of photochemical pollution as

well as the reports of the Implementation Committee referred to in

Article 9.

2. (a) The Parties shall, at sessions of the Executive Body, keep

under review the obligations set out in the present Protocol,

including:

(i) their obligations in relation to their calculated and

internationally optimised allocations of emission reductions

referred to in Article 7 (5);

(ii) the adequacy of the obligations and the progress made towards

the achievement of the objective of the present Protocol;

(b) Reviews shall take into account the best available scientific

information on the effects of acidification, eutrophication and

photochemical pollution, including assessments of all relevant

health effects, critical levels and loads, the development and

refinement of integrated assessment models, technological

developments, changing economic conditions, progress made on the

databases on emissions and abatement techniques, especially related

to ammonia and volatile organic compounds, and the fulfilment of the

obligations on emission levels;

(c) The procedures, methods and timing for such reviews shall be

specified by the Parties at a session of the Executive Body. The

first such review shall commence no later than one year after the

present Protocol enters into force.

 

Article 11

Settlement of disputes

1. In the event of a dispute between any two or more Parties

concerning the interpretation or application of the present

Protocol, the parties concerned shall seek a settlement of the

dispute through negotiation or any other peaceful means of their own

choice. The parties to the dispute shall inform the Executive Body

of their dispute.

2. When ratifying, accepting, approving or acceding to the present

Protocol, or at any time thereafter, a Party which is not a regional

economic integration organisation may declare in a written

instrument submitted to the Depositary that, in respect of any

dispute concerning the interpretation or application of the

Protocol, it recognises one or both of the following means of

dispute settlement as compulsory ipso facto and without special

agreement, in relation to any Party accepting the same obligation:

(a) submission of the dispute to the International Court of Justice;

 

(b) arbitration in accordance with procedures to be adopted by the

Parties at a session of the Executive Body, as soon as practicable,

in an annex on arbitration.

A Party which is a regional economic integration organisation may

make a declaration with like effect in relation to arbitration in

accordance with the procedures referred to in subparagraph (b).

3. A declaration made under paragraph (2) shall remain in force

until it expires in accordance with its terms or until three months

after written notice of its revocation has been deposited with the

Depositary.

4. A new declaration, a notice of revocation or the expiry of a

declaration shall not in any way affect proceedings pending before

the International Court of Justice or the arbitral tribunal, unless

the parties to the dispute agree otherwise.

5. Except in a case where the parties to a dispute have accepted the

same means of dispute settlement under paragraph (2), if after 12

months following notification by one party to another that a dispute

exists between them, the parties concerned have not been able to

settle their dispute through the means mentioned in paragraph (1),

the dispute shall be submitted, at the request of any of the parties

to the dispute, to conciliation.

6. For the purpose of paragraph (5), a conciliation commission shall

be created. The commission shall be composed of an equal number of

members appointed by each party concerned or, where parties in

conciliation share the same interest, by the group sharing that

interest, and a chairperson chosen jointly by the members so

appointed. The commission shall render a recommendatory award, which

the parties to the dispute shall consider in good faith.

 

Article 12

Annexes

The Annexes to the present Protocol shall form an integral part of

the Protocol.

 

Article 13

Amendments and adjustments

1. Any Party may propose amendments to the present Protocol. Any

Party to the Convention may propose an adjustment to Annex II to the

present Protocol to add to it its name, together with emission

levels, emission ceilings and percentage emission reductions.

2. Proposed amendments and adjustments shall be submitted in writing

to the Executive Secretary of the Commission, who shall communicate

them to all Parties. The Parties shall discuss the proposed

amendments and adjustments at the next session of the Executive

Body, provided that those proposals have been circulated by the

Executive Secretary to the Parties at least 90 days in advance.

3. Amendments to the present Protocol, including amendments to

Annexes II to IX, shall be adopted by consensus of the Parties

present at a session of the Executive Body, and shall enter into

force for the Parties which have accepted them on the 90th day after

the date on which two thirds of the Parties have deposited with the

Depositary their instruments of acceptance thereof. Amendments shall

enter into force for any other Party on the 90th day after the date

on which that Party has deposited its instrument of acceptance

thereof.

4. Amendments to the Annexes to the present Protocol, other than to

the Annexes referred to in paragraph 3, shall be adopted by

consensus of the Parties present at a session of the Executive Body.

On the expiry of 90 days from the date of its communication to all

Parties by the Executive Secretary of the Commission, an amendment

to any such Annex shall become effective for those Parties which

have not submitted to the Depositary a notification in accordance

with the provisions of paragraph (5), provided that at least 16

Parties have not submitted such a notification.

5. Any Party that is unable to approve an amendment to an Annex,

other than to an Annex referred to in paragraph (3), shall so notify

the Depositary in writing within 90 days from the date of the

communication of its adoption. The Depositary shall without delay

notify all Parties of any such notification received. A Party may at

any time substitute an acceptance for its previous notification and,

upon deposit of an instrument of acceptance with the Depositary, the

amendment to such an Annex shall become effective for that Party.

6. Adjustments to Annex II shall be adopted by consensus of the

Parties present at a session of the Executive Body and shall become

effective for all Parties to the present Protocol on the 90th day

following the date on which the Executive Secretary of the

Commission notifies those Parties in writing of the adoption of the

adjustment.

 

Article 14

Signature

1. The present Protocol shall be open for signature at Gothenburg

(Sweden) on 30 November and 1 December 1999, then at United Nations

Headquarters in New York until 30 May 2000, by States members of the

Commission as well as States having consultative status with the

Commission, pursuant to paragraph 8 of Economic and Social Council

Resolution 36 (IV) of 28 March 1947, and by regional economic

integration organisations, constituted by sovereign States members

of the Commission, which have competence in respect of the

negotiation, conclusion and application of international agreements

in matters covered by the Protocol, provided that the States and

organisations concerned are Parties to the Convention and are listed

in Annex II.

2. In matters within their competence, such regional economic

integration organisations shall, on their own behalf, exercise the

rights and fulfil the responsibilities which the present Protocol

attributes to their Member States. In such cases, the Member States

of these organisations shall not be entitled to exercise such rights

individually.

 

Article 15

Ratification, acceptance, approval and accession

1. The present Protocol shall be subject to ratification, acceptance

or approval by Signatories.

2. The present Protocol shall be open for accession as from 31 May

2000 by the States and organisations that meet the requirements of

Article 14 (1).

3. The instruments of ratification, acceptance, approval or

accession shall be deposited with the Depositary.

 

Article 16

Depositary

The Secretary-General of the United Nations shall be the Depositary.

 

Article 17

Entry into force

1. The present Protocol shall enter into force on the 90th day

following the date on which the 16th instrument of ratification,

acceptance, approval or accession has been deposited with the

Depositary.

2. For each State and organisation that meets the requirements of

Article 14 (1), which ratifies, accepts or approves the present

Protocol or accedes thereto after the deposit of the 16th instrument

of ratification, acceptance, approval or accession, the Protocol

shall enter into force on the 90th day following the date of deposit

by such Party of its instrument of ratification, acceptance,

approval or accession.

 

Article 18

Withdrawal

At any time after five years from the date on which the present

Protocol has come into force with respect to a Party, that Party may

withdraw from it by giving written notification to the Depositary.

Any such withdrawal shall take effect on the 90th day following the

date of its receipt by the Depositary, or on such later date as may

be specified in the notification of the withdrawal.

 

Article 19

Authentic texts

The original of the present Protocol, of which the English, French

and Russian texts are equally authentic, shall be deposited with the

Secretary-General of the United Nations.

 

 

 

IN WITNESS WHEREOF the undersigned, being duly authorised thereto,

have signed the present Protocol.

Done at Gothenburg (Sweden), this thirtieth day of November one

thousand nine hundred and ninety-nine.

 

 

ANNEX I

 

CRITICAL LOADS AND LEVELS

I. CRITICAL LOADS OF ACIDITY

A. For Parties within the geographical scope of EMEP

1. Critical loads (as defined in Article 1) of acidity for

ecosystems are determined in accordance with the Convention's Manual

on methodologies and criteria for mapping critical levels/loads and

geographical areas where they are exceeded. They are the maximum

amount of acidifying deposition an ecosystem can tolerate in the

long term without being damaged. Critical loads of acidity in terms

of nitrogen take account of nitrogen removal processes within an

ecosystem (e.g. uptake by plants). Critical loads of acidity in

terms of sulphur do not. A combined sulphur and nitrogen critical

load of acidity considers nitrogen only when the nitrogen deposition

is greater than the ecosystem nitrogen-removal processes. All

critical loads reported by Parties are summarised for use in the

integrated assessment modelling employed to provide guidance for

setting the emission ceilings in Annex II.

B. For Parties in North America

2. For eastern Canada, critical sulphur plus nitrogen loads for

forested ecosystems have been determined with scientific

methodologies and criteria (1997 Canadian Acid Rain Assessment)

similar to those in the Convention's Manual on methodologies and

criteria for mapping critical levels/loads and geographical areas

where they are exceeded. Eastern Canada critical-load values (as

defined in Article 1) of acidity are for sulphate in precipitation

expressed in kg/ha/year. Alberta in western Canada, where deposition

levels are currently below the environmental limits, has adopted the

generic critical-load classification systems used for soils in

Europe for potential acidity. Potential acidity is defined by

subtracting the total (both wet and dry) deposition of base cations

from that of sulphur and nitrogen. In addition to critical loads for

potential acidity, Alberta has established target and monitoring

loads for managing acidifying emissions.

3. For the United States of America, the effects of acidification

are evaluated through an assessment of the sensitivity of

ecosystems, the total loading within ecosystems of acidifying

compounds and the uncertainty associated with nitrogen-removal

processes within ecosystems.

4. These loads and effects are used in integrated assessment

modelling and provide guidance for setting the emission ceilings

and/or reductions for Canada and the United States of America in

Annex II.

II. CRITICAL LOADS OF NUTRIENT NITROGEN

For Parties within the geographical scope of EMEP

5. Critical loads (as defined in Article 1) of nutrient nitrogen

(eutrophication) for ecosystems are determined in accordance with

the Convention's Manual on methodologies and criteria for mapping

critical levels/loads and geographical areas where they are

exceeded. They are the maximum amount of eutrophying nitrogen

deposition an ecosystem can tolerate in the long term without being

damaged. All critical loads reported by Parties are summarised for

use in the integrated assessment modelling employed to provide

guidance for setting the emission ceilings in Annex II.

III. CRITICAL LEVELS OF OZONE

A. For Parties within the geographical scope of EMEP

6. Critical levels (as defined in Article 1) of ozone are determined

to protect plants in accordance with the Convention's Manual on

methodologies and criteria for mapping critical levels/loads and

geographical areas where they are exceeded. They are expressed as a

cumulative exposure over a threshold ozone concentration of 40 ppb

(parts per billion by volume). This exposure index is referred to as

AOT40 (accumulated exposure over a threshold of 40 ppb). The AOT40

is calculated as the sum of the differences between the hourly

concentration (in ppb) and 40 ppb for each hour when the

concentration exceeds 40 ppb.

7. The long-term critical level of ozone for crops of an AOT40 of

3000 ppb.hours for May to July (used as a typical growing season)

and for daylight hours was used to define areas at risk where the

critical level is exceeded. A specific reduction of exceedances was

targeted in the integrated assessment modelling undertaken for the

present Protocol to provide guidance for setting the emission

ceilings in Annex II. The long-term critical level of ozone for

crops is considered also to protect other plants such as trees and

natural vegetation. Further scientific work is under way to develop

a more differentiated interpretation of exceedances of critical

levels of ozone for vegetation.

8. A critical level of ozone for human health is represented by the

WHO Air Quality Guideline level for ozone of 120 >ISO_7>ü>ISO_1>g/m3

as an eight-hour average. In collaboration with the World Health

Organisation's Regional Office for Europe (WHO/EURO), a critical

level expressed as an AOT60 (accumulated exposure over a threshold

of 60 ppb), i.e. 120 >ISO_7>ü>ISO_1>g/m3, calculated over one year,

was adopted as a surrogate for the WHO Air Quality Guideline for the

purpose of integrated assessment modelling. This was used to define

areas at risk where the critical level is exceeded. A specific

reduction of these exceedances was targeted in the integrated

assessment modelling undertaken for the present Protocol to provide

guidance for setting the emission ceilings in Annex II.

B. For Parties in North America

9. For Canada, critical levels of ozone are determined to protect

human health and the environment and are used to establish a

Canada-wide Standard for ozone. The emission ceilings in Annex II

are defined according to the ambition level required to achieve the

Canada-wide Standard for ozone.

10. For the United States of America, critical levels of ozone are

determined to protect public health with an adequate margin of

safety, to protect public welfare from any known or expected adverse

effects, and are used to establish a National Ambient Air Quality

Standard. Integrated assessment modelling and the Air Quality

Standard are used in providing guidance for setting the emission

ceilings and/or reductions for the United States of America in Annex

II.

 

 

ANNEX II

 

EMISSION CEILINGS

The emission ceilings listed in the tables below relate to the

provisions of Article 3 (1) and (10), of the present Protocol. The

1980 and 1990 emission levels and the percentage emission reductions

listed are given for information purposes only.

Table 1. Emission ceilings for sulphur (thousands of tonnes of SO2

per year)

>TABLE POSITION>

Table 2. Emission ceilings for nitrogen oxides (thousands of tonnes

of NO2 per year)

>TABLE POSITION>

Table 3. Emission ceilings for ammonia (thousands of tonnes of NH3

per year)

>TABLE POSITION>

Table 4. Emission ceilings for volatile organic compounds (thousands

of tonnes of VOC per year)

>TABLE POSITION>

 

 

ANNEX III

 

DESIGNATED POLLUTANT EMISSIONS MANAGEMENT AREA (PEMA)

The following PEMA is listed for the purpose of the present

Protocol:

Russian Federation PEMA

This is the area of Murmansk oblast, the Republic of Karelia,

Leningrad oblast (including St. Petersburg), Pskov oblast, Novgorod

oblast and Kaliningrad oblast. The boundary of the PEMA coincides

with the State and administrative boundaries of these constituent

entities of the Russian Federation.

 

 

ANNEX IV

 

LIMIT VALUES FOR EMISSIONS OF SULPHUR FROM STATIONARY SOURCES

1. Section A applies to Parties other than Canada and the United

States of America, section B applies to Canada and section C applies

to the United States of America.

A. Parties other than Canada and the United States of America

2. For the purpose of section A, except Table 2 and paragraphs (11)

and (12), limit value means the quantity of a gaseous substance

contained in the waste gases from an installation that is not to be

exceeded. Unless otherwise specified, it shall be calculated in

terms of mass of pollutant per volume of the waste gases (expressed

as mg/m3), assuming standard conditions for temperature and pressure

for dry gas (volume at 273,15 K, 101,3 kPa). With regard to the

oxygen content of the exhaust gas, the values given in the tables

below for each source category shall apply. Dilution for the purpose

of lowering concentrations of pollutants in waste gases is not

permitted. Start-up, shutdown and maintenance of equipment are

excluded.

3. Emissions shall be monitored in all cases(1). Compliance with

limit values shall be verified. The methods of verification can

include continuous or discontinuous measurements, type approval, or

any other technically sound method.

4. Sampling and analysis of pollutants, as well as reference

measurement methods to calibrate any measurement system, shall be

carried out in accordance with the standards laid down by the

European Committee for Standardisation (CEN) or by the International

Organisation for Standardisation (ISO). While awaiting the

development of CEN or ISO standards, national standards shall apply.

5. Measurements of emissions should be carried out continuously when

emissions of SO2 exceed 75 kg/h.

6. In the case of continuous measurement for new plants, compliance

with the emission standards is achieved if the calculated daily mean

values do not exceed the limit value and if no hourly value exceeds

the limit value by 100 %.

7. In the case of continuous measurements for existing plants,

compliance with the emission standards is achieved if (a) none of

the monthly mean values exceeds the limit values; and (b) 97 % of

all the 48-hour mean values do not exceed 110 % of the limit values.

8. In the case of discontinuous measurements, as a minimum

requirement, compliance with the emission standards is achieved if

the mean value based on an appropriate number of measurements under

representative conditions does not exceed the value of the emission

standard.

9. Boilers and process heaters with a rated thermal input exceeding

50 Mwth:

Table 1. Limit values for SOx emissions released from boilers((In

particular, the limit values shall not apply to:

- plants in which the products of combustion are used for direct

heating, drying, or any other treatment of objects or materials,

e.g. reheating furnaces, furnaces for heat treatment,

- post-combustion plants, i.e. any technical apparatus designed to

purify the waste gases by combustion that is not operated as an

independent combustion plant,

- facilities for the regeneration of catalytic cracking catalysts; ,

- facilities for the conversion of hydrogen sulphide into sulphur,

- reactors used in the chemical industry,

- coke battery furnaces,

- cowpers,

- waste incinerators,

- plants powered by diesel, petrol or gas engines or by combustion

turbines, irrespective of the fuel used.))

>TABLE POSITION>

10. Gas oil:

Table 2. Limit values for the sulphur content of gas oil(("Gas oil"

means any petroleum product within HS 2710, or any petroleum product

which, by reason of its distillation limits, falls within the

category of middle distillates intended for use as fuel and of which

at least 85 % by volume, including distillation losses, distils at

350 °C. Fuels used in on-road and non-road vehicles and agricultural

tractors are excluded from this definition. Gas oil intended for

marine use is included in the definition if it meets the description

above or it has a viscosity or density falling within the ranges of

viscosity or density defined for marine distillates in Table I of

ISO 8217 (1996).))

>TABLE POSITION>

11. Claus plant: for a plant that produces more than 50 Mg of

sulphur a day:

(a) sulphur recovery 99,5 % for new plant;

(b) sulphur recovery 97 % for existing plant.

12. Titanium dioxide production: in new and existing installations,

discharges arising from digestion and calcination steps in the

manufacture of titanium dioxide shall be reduced to a value of not

more than 10 kg of SO2-equivalent per Mg of titanium dioxide

produced.

B. Canada

13. Limit values for controlling emissions of sulphur dioxide from

new stationary sources in the following stationary source category

will be determined on the basis of available information on control

technology and levels including limit values applied in other

countries and the following document: Canada Gazette, Part I.

Department of the Environment. Thermal Power Generation Emissions -

National Guidelines for New Stationary Sources. May 15, 1993, pp.

1633-1638.

C. United States of America

14. Limit values for controlling emissions of sulphur dioxide from

new stationary sources in the following stationarysource categories

are specified in the following documents:

(1) Electric Utility Steam Generating Units - 40 Code of Federal

Regulations (C.F.R.) Part 60, Subpart D, and Subpart Da;

(2) Industrial-Commercial-Institutional Steam Generating Units - 40

C.F.R. Part 60, Subpart Db, and Subpart Dc;

(3) Sulphuric Acid Plants - 40 C.F.R. Part 60, Subpart H;

(4) Petroleum Refineries - 40 C.F.R. Part 60, Subpart J;

(5) Primary Copper Smelters - 40 C.F.R. Part 60, Subpart P;

(6) Primary Zinc Smelters - 40 C.F.R. Part 60, Subpart Q;

(7) Primary Lead Smelters - 40 C.F.R. Part 60, Subpart R;

(8) Stationary Gas Turbines - 40 C.F.R. Part 60, Subpart GG;

(9) Onshore Natural Gas Processing - 40 C.F.R. Part 60, Subpart LLL;

 

(10) Municipal Waste Combustors - 40 C.F.R. Part 60, Subpart Ea, and

Subpart Eb;

(11) Hospital/Medical/Infectious Waste Incinerators - 40 C.F.R. Part

60, Subpart Ec.

 

(1) Monitoring is to be understood as an overall activity,

comprising measuring of emissions, mass balancing, etc. It can be

carried out continuously or discontinuously.

ANNEX V

 

LIMIT VALUES FOR EMISSIONS OF NITROGEN OXIDES FROM STATIONARY

SOURCES

1. Section A applies to Parties other than Canada and the United

States of America, section B applies to Canada and section C applies

to the United States of America.

A. Parties other than Canada and the United States of America

2. For the purpose of section A, limit value means the quantity of a

gaseous substance contained in the waste gases from an installation

that is not to be exceeded. Unless otherwise specified, it shall be

calculated in terms of mass of pollutant per volume of the waste

gases (expressed as mg/m3), assuming standard conditions for

temperature and pressure for dry gas (volume at 273,15 K, 101,3

kPa). With regard to the oxygen content of exhaust gas, the values

given in the tables below for each source category shall apply.

Dilution for the purpose of lowering concentrations of pollutants in

waste gases is not permitted. Limit values generally address NO

together with NO2, commonly named NOx, expressed as NO2. Start-up,

shutdown and maintenance of equipment are excluded.

3. Emissions shall be monitored in all cases(1). Compliance with

limit values shall be verified. The methods of verification can

include continuous or discontinuous measurements, type approval, or

any other technically sound method.

4. Sampling and analysis of pollutants, as well as reference

measurement methods to calibrate any measurement system, shall be

carried out in accordance with the standards laid down by the

European Committee for Standardisation (CEN) or by the International

Organisation for Standardisation (ISO). While awaiting the

development of CEN or ISO standards, national standards shall apply.

5. Measurements of emissions should be carried out continuously when

emissions of NOx exceed 75 kg/h.

6. In the case of continuous measurements, except for existing

combustion plant covered in Table 1, compliance with the emission

standards is achieved if the calculated daily mean values do not

exceed the limit value and if no hourly value exceeds the limit

value by 100 %.

7. In the case of continuous measurements for existing combustion

plants covered in Table 1, compliance with the emission standards is

achieved if (a) none of the monthly mean values exceeds the emission

limit values; and (b) 95 % of all the 48-hour mean values do not

exceed 110 % of the emission limit values.

8. In the case of discontinuous measurements, as a minimum

requirement, compliance with the emission standards is achieved if

the mean value based on an appropriate number of measurements under

representative conditions does not exceed the value of the emission

standard.

9. Boilers and process heaters with a rated thermal input exceeding

50 MWth:

Table 1. Limit values for NOx emissions released from boilers((In

particular, the limit values shall not apply to:

- plants in which the products of combustion are used for direct

heating, drying, or any other treatment of objects or materials,

e.g. reheating furnaces, furnaces for heat treatment,

- post-combustion plants, i.e. any technical apparatus designed to

purify the waste gases by combustion that is not operated as an

independent combustion plant,

- facilities for the regeneration of catalytic cracking catalysts,

- facilities for the conversion of hydrogen sulphide into sulphur,

- reactors used in the chemical industry,

- coke battery furnaces,

- cowpers,

- waste incinerators,

- plants powered by diesel, petrol or gas engines or by combustion

turbines, irrespective of the fuel used.))

>TABLE POSITION>

10. Onshore combustion turbines with a rated thermal input exceeding

50 MWth: the NOx limit values expressed in mg/Nm3 (with an O2

content of 15 %) are to be applied to a single turbine. The limit

values in Table 2 apply only above 70 % load.

Table 2. Limit values for NOx emissions released from onshore

combustion turbines

>TABLE POSITION>

11. Cement production:

Table 3. Limit values for NOx emissions released from cement

production((Installations for the production of cement clinker in

rotary kilns with a capacity > 500 mg/day or in other furnaces with

a capacity > 50 Mg/day.))

>TABLE POSITION>

12. Stationary engines:

Table 4. Limit values for NOx emissions released from new stationary

engines

>TABLE POSITION>

13. Production and processing of metals:

Table 5. Limit values for NOx emissions released from primary iron

and steel production((Production and processing of metals: metal ore

roasting or sintering installations, installations for the

production of pig iron or steel (primary or secondary fusion)

including continuous casting with a capacity exceeding 2,5 Mg/hour,

installations for the processing of ferrous metals (hot rolling

mills > 20 Mg/hour of crude steel).))

>TABLE POSITION>

14. Nitric acid production:

Table 6. Limit values for NOx emissions released from nitric acid

production excluding acid concentration units

>TABLE POSITION>

B. Canada

15. Limit values for controlling emissions of nitrogen oxides (NOx)

from new stationary sources in the following stationary source

categories will be determined on the basis of available information

on control technology and levels including limit values applied in

other countries and the following documents:

(a) Canadian Council of Ministers of the Environment (CCME).

National Emission Guidelines for Stationary Combustion Turbines.

December 1992. PN1072;

(b) Canada Gazette, Part I. Department of the Environment. Thermal

Power Generation Emissions - National Guidelines for New Stationary

Sources. May 15, 1993, pp. 1633-1638;

(c) CCME. National Emission Guidelines for Cement Kilns. March 1998.

PN1284.

C. United States of America

16. Limit values for controlling emissions of NOx from new

stationary sources in the followingstationary source categories are

specified in the following documents:

(a) Coal-fired Utility Units - 40 Code of Federal Regulations

(C.F.R.) Part 76;

(b) Electric Utility Steam Generating Units - 40 C.F.R. Part 60,

Subpart D, and Subpart Da;

(c) Industrial-Commercial-Institutional Steam Generating Units - 40

C.F.R. Part 60, Subpart Db;

(d) Nitric Acid Plants - 40 C.F.R. Part 60, Subpart G;

(e) Stationary Gas Turbines - 40 C.F.R. Part 60, Subpart GG;

(f) Municipal Waste Combustors - 40 C.F.R. Part 60, Subpart Ea, and

Subpart Eb;

(g) Hospital/Medical/Infectious Waste Incinerators - 40 C.F.R. Part

60, Subpart Ec.

 

(1) Monitoring is to be understood as an overall activity,

comprising measuring of emissions, mass balancing, etc. It can be

carried out continuously or discontinuously.

ANNEX VI

 

LIMIT VALUES FOR EMISSIONS OF VOLATILE ORGANIC COMPOUNDS FROM

STATIONARY SOURCES

1. Section A applies to Parties other than Canada and the United

States of America, section B applies to Canada and section C applies

to the United States of America.

A. Parties other than Canada and the United States of America

2. This section of the present Annex covers the stationary sources

of non-methane volatile organic compound (NMVOC) emissions listed in

paragraphs (8) to (21) below. Installations or parts of

installations for research, development and testing of new products

and processes are not covered. Threshold values are given in the

sector-specific tables below. They generally refer to solvent

consumption or emission mass flow. Where one operator carries out

several activities falling under the same subheading at the same

installation on the same site, the solvent consumption or emission

mass flow of such activities are added together. If no threshold

value is indicated, the given limit value applies to all the

installations concerned.

3. For the purpose of section A of the present Annex:

(a) "storage and distribution of petrol" means the loading of

trucks, railway wagons, barges and seagoing ships at depots and

mineral oil refinery dispatch stations, excluding vehicle refuelling

at service stations covered by relevant documents on mobile sources;

 

(b) "adhesive coating" means any process in which an adhesive is

applied to a surface, with the exception of adhesive coating and

laminating associated with printing processes and wood and plastic

lamination;

(c) "wood and plastic lamination" means any process to adhere

together wood and/or plastic to produce laminated products;

(d) "coating processes" means the application of metal and plastic

surfaces to: passenger cars, truck cabins, trucks, buses or wooden

surfaces and covers any process in which a single or multiple

application of a continuous film of coating is laid onto:

(i) new vehicles (see below) defined as vehicles of category M1 and

of category N1 insofar as they are coated at the same installation

as M1 vehicles;

(ii) truck cabins, defined as the housing for the driver, and all

integrated housing for the technical equipment of category N2 and N3

vehicles;

(iii) vans and trucks defined as category N1, N2 and N3 vehicles,

but excluding truck cabins;

(iv) buses defined as category M2 and M3 vehicles;

(v) other metallic and plastic surfaces including those of

aeroplanes, ships, trains, etc., wooden surfaces, textile, fabric,

film and paper surfaces.

This source category does not include the coating of substrates with

metals by electrophoretic or chemical spraying techniques. If the

coating process includes a step in which the same article is

printed, that printing step is considered part of the coating

process. However, printing processes operated as a separate activity

are not included. In this definition:

- M1 vehicles are those used for the carriage of passengers and

comprising not more than eight seats in addition to the driver's

seat,

- M2 vehicles are those used for the carriage of passengers and

comprising more than eight seats in addition to the driver's seat,

and having a maximum mass not exceeding 5 Mg,

- M3 vehicles are those used for the carriage of passengers and

comprising more than eight seats in addition to the driver's seat,

and having a maximum mass exceeding 5 Mg,

- N1 vehicles are those used for the carriage of goods and having a

maximum mass not exceeding 3,5 Mg,

- N2 vehicles are those used for the carriage of goods and having a

maximum mass exceeding 3,5 Mg but not exceeding 12 Mg,

- N3 vehicles are those used for the carriage of goods and having a

maximum mass exceeding 12 Mg.

(e) "coil coating" means any processes where coiled steel, stainless

steel, coated steel, copper alloys or aluminium strip is coated with

either a film-forming or laminate coating in a continuous process;

(f) "dry cleaning" means any industrial or commercial process using

VOCs in an installation to clean garments, furnishings and similar

consumer goods with the exception of the manual removal of stains

and spots in the textile and clothing industry;

(g) "manufacturing of coatings, varnishes, inks and adhesives" means

the manufacture of coating preparations, varnishes, inks and

adhesives, and of intermediates as far as they are produced in the

same installation by mixing pigments, resins and adhesive materials

with organic solvents or other carriers. This category also includes

dispersion, predispersion, realization of a certain viscosity or

colour and packing the final products in containers;

(h) "printing" means any process of reproduction of text and/or

images in which, with the use of an image carrier, ink is

transferred onto a surface and applies to the following

subprocesses:

(i) flexography: a printing process using an image carrier of rubber

or elastic photopolymers on which the printing inks are above the

non-printing areas, using liquid inks that dry through evaporation;

(ii) heat set web offset: a web-fed printing process using an image

carrier in which the printing and non-printing areas are in the same

plane, where web-fed means that the material to be printed is fed to

the machine from a reel as distinct from separate sheets. The

non-printing area is treated to attract water and thus reject ink.

The printing area is treated to receive and transmit ink to the

surface to be printed. Evaporation takes place in an oven where hot

air is used to heat the printed material;

(iii) publication rotogravure: rotogravure used for printing paper

for magazines, brochures, catalogues or similar products, using

toluene-based inks;

(iv) rotogravure: a printing process using a cylindrical image

carrier in which the printing area is below the non-printing area,

using liquid inks that dry through evaporation. The recesses are

filled with ink and the surplus is cleaned off the non-printing area

before the surface to be printed contacts the cylinder and lifts the

ink from the recesses;

(v) rotary screen printing: a web-fed printing process in which the

ink is passed onto the surface to be printed by forcing it through a

porous image carrier, in which the printing area is open and the

non-printing area is sealed off, using liquid inks that dry only

through evaporation. Web-fed means that the material to be printed

is fed to the machine from a reel as distinct from separate sheets;

(vi) laminating associated to a printing process: the adhering of

two or more flexible materials to produce laminates;

(vii) varnishing: a process by which a varnish or an adhesive

coating is applied to a flexible material for the purpose of later

sealing the packaging material;

(i) "manufacturing of pharmaceutical products" means chemical

synthesis, fermentation, extraction, formulation and finishing of

pharmaceutical products and, where carried out at the same site, the

manufacture of intermediate products;

(j) "conversion of natural or synthetic rubber" means any process of

mixing, crushing, blending, calendering, extruding and vulcanisation

of natural or synthetic rubber and additionally processes for the

processing of natural or synthetic rubber to derive an end product;

(k) "surface cleaning" means any process except dry cleaning using

organic solvents to remove contamination from the surface of

material, including degreasing; a cleaning process consisting of

more than one step before or after any other processing step is

considered as one surface-cleaning process. The process refers to

the cleaning of the surface of products and not to the cleaning of

process equipment;

(l) "extraction of vegetable oil and animal fat and refining of

vegetable oil" means the extraction of vegetable oil from seeds and

other vegetable matter, the processing of dry residues to produce

animal feed, and the purification of fats and vegetable oils derived

from seeds, vegetable matter and/or animal matter;

(m) "vehicle refinishing" means any industrial or commercial coating

activity and associated degreasing activities performing:

(i) the coating of road vehicles, or part of them, carried out as

part of vehicle repair, conservation or decoration outside

manufacturing installations, or

(ii) the original coating of road vehicles, or part of them, with

refinishing-type materials, where this is carried out away from the

original manufacturing line, or

(iii) the coating of trailers (including semi-trailers);

(n) "impregnation of wooden surfaces" means any process impregnating

timber with preservative;

(o) "standard conditions" means a temperature of 273,15 K and a

pressure of 101,3 kPa;

(p) "NMVOCs" comprise all organic compounds except methane which at

273,15 K show a vapour pressure of at least 0,01 kPa or which show a

comparable volatility under the given application conditions;

(q) "waste gas" means the final gaseous discharge containing NMVOCs

or other pollutants from a stack or from emission abatement

equipment into air. The volumetric flow rates shall be expressed in

m3/h at standard conditions;

(r) "fugitive emission of NMVOCs" means any emission, not in waste

gases, of NMVOC into air, soil and water as well as, unless

otherwise stated, solvents contained in any product, and includes

uncaptured emissions of NMVOCs released to the outside environment

via windows, doors, vents and similar openings. Fugitive limit

values are calculated on the basis of a solvent management plan (see

Appendix I to the present Annex);

(s) "total emission of NMVOCs" means the sum of fugitive emission of

NMVOCs and emission of NMVOCs in waste gases;

(t) "input" means the quantity of organic solvents and their

quantity in preparations used when carrying out a process, including

the solvents recycled inside and outside the installation, and which

are counted every time they are used to carry out the activity;

(u) "limit value" means the maximum quantity of a gaseous substance

contained in the waste gases from an installation which is not to be

exceeded during normal operation. Unless otherwise specified, it

shall be calculated in terms of mass of pollutant per volume of the

waste gases (expressed as mg C/Nm3 unless specified otherwise),

assuming standard conditions for temperature and pressure for dry

gas. For solvent-using installations, limit values are given as mass

unit per characteristic unit of the respective activity. Gas volumes

that are added to the waste gas for cooling or dilution purposes

shall not be considered when determining the mass concentration of

the pollutant in the waste gas. Limit values generally address all

volatile organic compounds except methane (no further distinction is

made, e.g. in terms of reactivity or toxicity);

(v) "normal operation" means all periods of operation except

start-up and shutdown operations and maintenance of equipment;

(w) "substances harmful to human health" are subdivided into two

categories:

(i) halogenated VOCs that have the possible risk of irreversible

effects; or

(ii) hazardous substances that are carcinogens, mutagens or toxic to

reproduction or that may cause cancer, may cause heritable genetic

damage, may cause cancer by inhalation, may impair fertility or may

cause harm to the unborn child.

4. The following requirements shall be satisfied:

(a) emissions of NMVOCs shall be monitored(1) and compliance with

limit values shall be verified. The methods of verification may

include continuous or discontinuous measurements, type approval or

any other technically sound method; furthermore, they shall be

economically viable;

(b) the concentrations of air pollutants in gas-carrying ducts shall

be measured in a representative way. Sampling and analysis of all

pollutants, as well as reference measurement methods to calibrate

any measurement system, shall be carried out according to the

standards laid down by the European Committee for Standardisation

(CEN) or by the International Organisation for Standardisation

(ISO). While awaiting the development of CEN or ISO standards,

national standards shall apply;

(c) if measurements of emissions of NMVOCs are required, they should

be carried out continuously if emissions of NMVOCs exceed 10 kg of

total organic carbon (TOC)/h in the exhaust duct downstream from an

emission reduction installation and the hours of operation exceed

200 hours a year. For all other installations, discontinuous

measurement is required as a minimum. For the approval of

compliance, own approaches may be used provided that they result in

equal stringency;

(d) in the case of continuous measurements, as a minimum

requirement, compliance with the emission standards is achieved if

the daily mean does not exceed the limit value during normal

operation and no hourly average exceeds the limit values by 150 %.

For the approval of compliance, own approaches may be used provided

that they result in equal stringency;

(e) in the case of discontinuous measurements, as a minimum

requirement, compliance with the emission standards is achieved if

the mean value of all readings does not exceed the limit value and

no hourly mean exceeds the limit value by 150 %. For the approval of

compliance, own approaches may be used provided that they result in

equal stringency;

(f) all appropriate precautions shall be taken to minimize emissions

of NMVOCs during start-up and shutdown, and in case of deviations

from normal operation;

(g) measurements are not required if end-of-pipe abatement equipment

is not needed to comply with the limit values below and it can be

shown that limit values are not exceeded.

5. The following limit values should be applied for waste gases,

unless stated otherwise below:

(a) 20 mg substance/m3 for discharges of halogenated volatile

organic compounds (which are assigned the risk phrase "possible risk

of irreversible effects"), where the mass flow of the sum of the

considered compounds is greater than or equal to 100 g/h;

(b) 2 mg/m3 (expressed as the mass sum of individual compounds) for

discharges of volatile organic compounds (which are assigned the

following risk phrases: may cause cancer, heritable genetic damage,

cancer by inhalation or harm to the unborn child; may impair

fertility), where the mass flow of the sum of the considered

compounds is greater than or equal to 10 g/h.

6. For the source categories listed in paragraphs (9) to (21) below,

the following revisions are relevant:

(a) instead of applying the limit values for installations set out

below, the operators of the respective installations may be allowed

to use a reduction scheme (see Appendix II to the present Annex).

The purpose of a reduction scheme is to give the operator the

possibility to achieve by other means emission reductions equivalent

to those achieved if given limit values were to be applied;

(b) for fugitive emissions of NMVOCs, the fugitive emission values

set out below shall be applied as a limit value. However, where it

is demonstrated to the satisfaction of the competent authority that

for an individual installation this value is not technically and

economically feasible, the competent authority may exempt that

installation provided that significant risks to human health or the

environment are not expected. For each derogation, the operator must

demonstrate to the satisfaction of the competent authority that the

best available technique is used.

7. The limit values for VOC emissions for the source categories

defined in paragraph (3) shall be as specified in paragraphs (8) to

(21) below.

8. Storage and distribution of petrol:

Table 1. Limit values for VOC emissions released from the storage

and distribution of petrol, excluding the loading of seagoing ships

>TABLE POSITION>

Note:

The vapour displaced by the filling of petrol storage tanks shall be

displaced either into other storage tanks or into abatement

equipment meeting the limit values in the table above.

9. Adhesive coating:

Table 2. Limit values for NMVOC emissions released from adhesive

coating

>TABLE POSITION>

10. Wood and plastic lamination:

Table 3. Limit values for NMVOC emissions released from wood and

plastic lamination

>TABLE POSITION>

11. Coating processes (metal and plastic surfaces in passenger cars,

truck cabins, trucks, buses, wooden surfaces):

Table 4. Limit values for NMVOC emissions released from coating

processes in the car industry

>TABLE POSITION>

Table 5. Limit values for NMVOC emissions released from coating

processes in various industrial sectors

>TABLE POSITION>

12. Coil coating:

Table 6. Limit values for NMVOC emissions released from coil coating

>TABLE POSITION>

13. Dry cleaning:

Table 7. Limit values for NMVOC emissions released from dry cleaning

>TABLE POSITION>

14. Manufacturing of coatings, varnishes, inks and adhesives:

Table 8. Limit values for NMVOC emissions released from

manufacturing of coatings, varnishes, inks and adhesives

>TABLE POSITION>

15. Printing (flexography, heat set web offset, publication

rotogravure etc.):

Table 9. Limit values for NMVOC emissions released from printing

processes

>TABLE POSITION>

16. Manufacturing of pharmaceutical products:

Table 10. Limit values for NMVOC emissions released from

manufacturing of pharmaceutical products

>TABLE POSITION>

17. Conversion of natural or synthetic rubber:

Table 11. Limit values for NMVOC emission released from conversion

of natural or synthetic rubber

>TABLE POSITION>

18. Surface cleaning:

Table 12. Limit values for NMVOC emissions released from surface

cleaning

>TABLE POSITION>

19. Vegetable oil and animal fat extraction and vegetable oil

refining processes:

Table 13. Limit values for NMVOC emissions released from extraction

of vegetable and animal fat and refining of vegetable oil

>TABLE POSITION>

20. Vehicle refinishing:

Table 14. Limit values for NMVOC emissions released from vehicle

refinishing

>TABLE POSITION>

21. Impregnation of wooden surfaces:

Table 15. Limit values for NMVOC emissions released from

impregnation of wooden surfaces

>TABLE POSITION>

B. Canada

22. Limit values for controlling emissions of volatile organic

compounds (VOCs) from new stationary sources in the following

stationary source categories will be determined on the basis of

available information on control technology and levels, including

limit values applied in other countries, and the following

documents:

(a) Canadian Council of Ministers of the Environment (CCME).

Environmental Code of Practice for the Reduction of Solvent

Emissions from Dry Cleaning Facilities. December 1992. PN1053;

(b) CCME. Environmental Guideline for the Control of Volatile

Organic Compounds Process Emissions from New Organic Chemical

Operations. September 1993. PN1108;

(c) CCME. Environmental Code of Practice for the Measurement and

Control of Fugitive VOC Emissions from Equipment Leaks. October

1993. PN1106;

(d) CCME. A Program to Reduce Volatile Organic Compound Emissions by

40 Percent from Adhesives and Sealants. March 1994. PN1116;

(e) CCME. A Plan to Reduce Volatile Organic Compound Emissions by 20

Percent from Consumer Surface Coatings. March 1994. PN1114;

(f) CCME. Environmental Guidelines for Controlling Emissions of

Volatile Organic Compounds from Aboveground Storage Tanks. June

1995. PN1180;

(g) CCME. Environmental Code of Practice for Vapour Recovery during

Vehicle Refueling at Service Stations and Other Gasoline Dispersing

Facilities. (Stage II) April 1995. PN1184;

(h) CCME. Environmental Code of Practice for the Reduction of

Solvent Emissions from Commercial and Industrial Degreasing

Facilities. June 1995. PN1182;

(i) CCME. New Source Performance Standards and Guidelines for the

Reduction of Volatile Organic Compound Emissions from Canadian

Automotive Original Equipment Manufacturer (OEM) Coating Facilities.

August 1995. PN1234;

(j) CCME. Environmental Guideline for the Reduction of Volatile

Organic Compound Emissions from the Plastics Processing Industry.

July 1997. PN1276; and

(k) CCME. National Standards for the Volatile Organic Compound

Content of Canadian Commercial/Industrial Surface Coating Products -

Automotive Refinishing. August 1997. PN1288.

C. United States of America23. Limit values for controlling emissions of VOCs from new

stationary sources in the following stationary source categories are

specified in the following documents:

(a) Storage Vessels for Petroleum Liquids - 40 Code of Federal

Regulations (C.F.R.) Part 60, Subpart K, and Subpart Ka;

(b) Storage Vessels for Volatile Organic Liquids - 40 C.F.R. Part

60, Subpart Kb;

(c) Petroleum Refineries - 40 C.F.R. Part 60, Subpart J;

(d) Surface Coating of Metal Furniture - 40 C.F.R. Part 60, Subpart

EE;

(e) Surface Coating for Automobile and Light Duty Trucks - 40 C.F.R.

Part 60, Subpart MM;

(f) Publication Rotogravure Printing - 40 C.F.R. Part 60, Subpart

QQ;

(g) Pressure Sensitive Tape and Label Surface Coating Operations -

40 C.F.R. Part 60, Subpart RR;

(h) Large Appliance, Metal Coil and Beverage Can Surface Coating -

40 C.F.R. Part 60, Subpart SS, Subpart TT and Subpart WW;

(i) Bulk Gasoline Terminals - 40 C.F.R. Part 60, Subpart XX;

(j) Rubber Tire Manufacturing - 40 C.F.R. Part 60, Subpart BBB;

(k) Polymer Manufacturing - 40 C.F.R. Part 60, Subpart DDD;

(l) Flexible Vinyl and Urethane Coating and Printing - 40 C.F.R.

Part 60, Subpart FFF;

(m) Petroleum Refinery Equipment Leaks and Wastewater Systems - 40

C.F.R. Part 60, Subpart GGG and Subpart QQQ;

(n) Synthetic Fiber Production - 40 C.F.R. Part 60, Subpart HHH;

(o) Petroleum Dry Cleaners - 40 C.F.R. Part 60, Subpart JJJ;

(p) Onshore Natural Gas Processing Plants - 40 C.F.R. Part 60,

Subpart KKK;

(q) SOCMI Equipment Leaks, Air Oxidation Units, Distillation

Operations and Reactor Processes - 40 C.F.R. Part 60, Subpart VV,

Subpart III, Subpart NNN and Subpart RRR;

(r) Magnetic Tape Coating - 40 C.F.R. Part 60, Subpart SSS;

(s) Industrial Surface Coatings - 40 C.F.R. Part 60, Subpart TTT;

and

(t) Polymeric Coatings of Supporting Substrates Facilities - 40

C.F.R. Part 60, Subpart VVV.

 

(1) Monitoring is to be understood as an overall activity,

comprising measuring of emissions, mass balancing, etc. It can be

carried out continuously or discontinuously.

Appendix I

 

SOLVENT MANAGEMENT PLAN

Introduction

1. This Appendix to the Annex on limit values for emissions of

non-methane volatile organic compounds (NMVOCs) from stationary

sources provides guidance on carrying out a solvent management plan.

It identifies the principles to be applied (paragraph (2)), provides

a framework for the mass balance (paragraph (3)) and provides an

indication of the requirements for verification of compliance

(paragraph (4)).

Principles

2. The solvent management plan serves the following purposes:

(a) verification of compliance, as specified in the Annex;

(b) identification of future reduction options.

Definitions

3. The following definitions provide a framework for the mass

balance exercise:

(a) Inputs of organic solvents:

I1. The quantity of organic solvents or their quantity in

preparations purchased that are used as input into the process in

the time-frame over which the mass balance is being calculated.

I2. The quantity of organic solvents or their quantity in

preparations recovered and reused as solvent input into the process.

(The recycled solvent is counted every time it is used to carry out

the activity.)

(b) Outputs of organic solvents:

O1. Emission of NMVOCs in waste gases.

O2. Organic solvents lost in water, if appropriate taking into

account waste-water treatment when calculating O5.

O3. The quantity of organic solvents that remains as contamination

or residue in output of products from the process.

O4. Uncaptured emissions of organic solvents to air. This includes

the general ventilation of rooms, where air is released to the

outside environment via windows, doors, vents and similar openings.

O5. Organic solvents and/or organic compounds lost due to chemical

or physical reactions (including, for example, those that are

destroyed, e.g. by incineration or other waste-gas or waste-water

treatments, or captured, e.g. by adsorption, as long as they are not

counted under O6, O7 or O8).

O6. Organic solvents contained in collected waste.

O7. Organic solvents, or organic solvents contained in preparations,

that are sold or are intended to be sold as a commercially valuable

product.

O8. Organic solvents contained in preparations recovered for reuse

but not as input into the process, as long as they are not counted

under O7.

O9. Organic solvents released in other ways.

Guidance on use of the solvent management plan for verification of

compliance

4. The use of the solvent management plan will be determined by the

particular requirement which is to be verified, as follows:

(a) Verification of compliance with the reduction option mentioned

in paragraph (6)(a) of the Annex, with a total limit value expressed

in solvent emissions per unit product, or as otherwise stated in the

Annex.

(i) For all activities using the reduction option mentioned in

paragraph (6)(a) of the Annex, the solvent management plan should be

put into effect annually to determine consumption. Consumption can

be calculated by means of the following equation:

>REFERENCE TO A GRAPHIC>

A parallel exercise should also be undertaken to determine solids

used in coating in order to derive the annual reference emission and

the target emission each year;

(ii) for assessing compliance with a total limit value expressed in

solvent emissions per unit product or as otherwise stated in the

Annex, the solvent management plan should be put into effect

annually to determine emission of NMVOCs. Emission of NMVOCs can be

calculated by means of the following equation:

>REFERENCE TO A GRAPHIC>

Where F is the fugitive emission of NMVOC as defined in subparagraph

(b)(i) below. The emission figure should be divided by the relevant

product parameter;

(b) Determination of fugitive emission of NMVOCs for comparison with

fugitive emission values in the Annex:

(i) Methodology: The fugitive emission of NMVOC can be calculated by

means of the following equation:

>REFERENCE TO A GRAPHIC>

or

>REFERENCE TO A GRAPHIC>

This quantity can be determined by direct measurement of the

quantities. Alternatively, an equivalent calculation can be made by

other means, for instance by using the capture efficiency of the

process.

The fugitive emission value is expressed as a proportion of the

input, which can be calculated by means of the following equation:

>REFERENCE TO A GRAPHIC>

(ii) Frequency: Fugitive emission of NMVOCs can be determined by a

short but comprehensive set of measurements. This need not to be

done again until the equipment is modified.

 

 

Appendix II

 

REDUCTION SCHEME

Principles

1. The purpose of the reduction scheme is to allow the operator the

possibility to achieve by other means emission reductions equivalent

to those achieved if the limit values were to be applied. To that

end the operator may use any reduction scheme specially designed for

his installation, provided that in the end an equivalent emission

reduction is achieved. Parties shall report on progress in achieving

the same emission reduction, including experience with the

application of the reduction scheme.

Practice

2. If applying coatings, varnishes, adhesives or inks, the following

scheme can be used. Where it is inappropriate, the competent

authority may allow an operator to apply any alternative exemption

scheme which it is satisfied fulfils the principles outlined here.

The design of the scheme takes into account the following facts:

(a) where substitutes containing little or no solvent are still

under development, a time extension must be given to the operator to

implement his emission reduction plans;

(b) the reference point for emission reductions should correspond as

closely as possible to the emissions that would have resulted had no

reduction action been taken.

3. The following scheme shall operate for installations for which a

constant solid content of product can be assumed and used to define

the reference point for emission reductions.

(a) The operator shall forward an emission reduction plan which

includes in particular decreases in the average solvent content of

the total input and/or increased efficiency in the use of solids to

achieve a reduction of the total emissions from the installation to

a given percentage of annual reference emissions, termed the target

emission. This must be done in the following time frame:

>TABLE POSITION>

(b) The annual reference emission is calculated as follows:

(i) the total mass of solids in the quantity of coating and/or ink,

varnish or adhesive consumed in a year is determined. Solids are all

materials in coatings, inks, varnishes and adhesives that become

solid once the water or the volatile organic compounds are

evaporated;

(ii) the annual reference emissions are calculated by multiplying

the mass determined as in subparagraph (i) by the appropriate factor

listed in the table below. The competent authorities may adjust

these factors for individual installations to reflect documented

increased efficiency in the use of solids;

>TABLE POSITION>

(iii) the target emission is equal to the annual reference emission

multiplied by a percentage equal to:

- (The fugitive emission value + 15), for installations in the

following sectors:

- vehicle coating (solvent consumption < 15 Mg/year) and vehicle

refinishing,

- metal, plastic, textile, fabric, film and paper coating (solvent

consumption between 5 and 15 Mg/year),

- coating of wooden surfaces (solvent consumption between 15 and 25

Mg/year),

- (The fugitive emission value + 5) for all other installations;

(iv) compliance is achieved if the actual solvent emission

determined from the solvent management plan is less than or equal to

the target emission.

 

 

ANNEX VII

 

TIMESCALES UNDER ARTICLE 3

1. The timescales for the application of the limit values referred

to in Article 3(2) and (3), shall be:

(a) for new stationary sources, one year after the date of entry

into force of the present Protocol for the Party in question;

(b) for existing stationary sources:

(i) in the case of a Party that is not a country with an economy in

transition, one year after the date of entry into force of the

present Protocol or 31 December 2007, whichever is the later;

(ii) in the case of a Party that is a country with an economy in

transition, eight years after the entry into force of the present

Protocol.

2. The timescales for the application of the limit values for fuels

and new mobile sources referred to in Article 3(5), and the limit

values for gas oil referred to in Annex IV, Table 2, shall be:

(i) in the case of a Party that is not a country with an economy in

transition, the date of entry into force of the present Protocol or

the dates associated with the measures specified in Annex VIII and

with the limit values specified in Annex IV, Table 2, whichever is

the later; and

(ii) in the case of a Party that is a country with an economy in

transition, five years after the date of entry into force of the

present Protocol or five years after the dates associated with the

measures specified in Annex VIII and with the limit values in Annex

IV, Table 2, whichever is the later.

This timescale shall not apply to a Party to the present Protocol to

the extent that that Party is subject to a shorter timescale with

regard to gas oil under the Protocol on Further Reduction of Sulphur

Emissions.

3. For the purpose of the present Annex, "a country with an economy

in transition" means a Party that has made with its instrument of

ratification, acceptance, approval or accession a declaration that

it wishes to be treated as a country with an economy in transition

for the purposes of paragraphs (1) and/or (2) of this Annex.

 

 

ANNEX VIII

 

LIMIT VALUES FOR FUELS AND NEW MOBILE SOURCES

INTRODUCTION

1. Section A applies to Parties other than Canada and the United

States of America, section B applies to Canada and section C applies

to the United States of America.

2. The Annex contains limit values for NOx, expressed as nitrogen

dioxide (NO2) equivalents, and for hydrocarbons, most of which are

volatile organic compounds, as well as environmental specifications

for marketed fuels for vehicles.

3. The timescales for applying the limit values in this Annex are

laid down in Annex VII.

A. Parties other than Canada and the United States of America

Passenger cars and light-duty vehicles

4. Limit values for power-driven vehicles with at least four wheels

and used for the carriage of passengers (category M) and goods

(category N) are given in Table 1.

Heavy-duty vehicles

5. Limit values for engines for heavy-duty vehicles are given in

Tables 2 and 3 depending on the applicable test procedures.

Motorcycles and mopeds

6. Limit values for motorcycles and mopeds are given in Table 6 and

Table 7.

Non-road vehicles and machines

7. Limit values for agricultural and forestry tractors and other

non-road vehicle/machine engines are listed in Tables 4 and 5. Stage

I (Table 4) is based on ECE Regulation 96, "Uniform provisions

concerning the approval of compression-ignition (CI) engines to be

installed in agricultural and forestry tractors with regard to the

emissions of pollutants by the engine".

Fuel quality

8. Environmental quality specifications for petrol and diesel are

given in Tables 8 to 11.

Table 1. Limit values for passenger cars and light-duty vehicles

>TABLE POSITION>

Table 2. Limit values for heavy-duty vehicles - European

steady-state cycle (ESC) and European load-response (ELR) tests

>TABLE POSITION>

Table 3. Limit values for heavy-duty vehicles - European transient

cycle (ETC) test((The conditions for verifying the acceptability of

the ETC tests when measuring the emissions of gas-fuelled engines

against the limit values applicable in row A shall be re-examined

and, where necessary, modified in accordance with the procedure laid

down in Article 13 of Directive 70/156/EEC.))

>TABLE POSITION>

Table 4. Limit values (stage I) for diesel engines for non-road

mobile machines (measurement procedure ISO 8178)

>TABLE POSITION>

Note:

These limits are engine-out limits and shall be achieved before any

exhaust after-treatment service.

Table 5. Limit values (stage II) for diesel engines for non-road

mobile machines (measurement procedure ISO 8178)

>TABLE POSITION>

Table 6. Limit values for motorcycles and three- and four-wheelers (

> 50 cm3; > 45 km/h) to be applied from 17 June 1999((Type approval

shall be refused as from the given date if the vehicle's emissions

do not meet the limit values.))

>TABLE POSITION>

Note:

For three- and four-wheelers, the limit values have to be multiplied

by 1,5.

Table 7. Limit values for mopeds (< = 50 cm3; < 45 km/h)

>TABLE POSITION>

Table 8. Environmental specifications for marketed fuels to be used

for vehicles equipped with positive-ignition engines

Type: Petrol

>TABLE POSITION>

Note:

Parties shall ensure that, no later than 1 January 2000, petrol can

be marketed within their territory only if it complies with the

environmental specifications set out in Table 8. Where a Party

determines that banning petrol with a sulphur content which does not

comply with the specifications for sulphur content in Table 8, but

does not exceed the current content, would raise severe difficulties

for its industries in making the necessary changes in their

manufacturing facilities by 1 January 2000, it may extend the time

period of marketing within its territory until 1 January 2003 at the

latest. In such a case the Party shall specify, in a declaration to

be deposited together with its instrument of ratification,

acceptance, approval or accession, that it intends to extend the

time period and present written information on the reason for this

to the Executive Body.

Table 9. Environmental specifications for marketed fuels to be used

for vehicles equipped with compression-ignition engines

Type: Diesel fuel

>TABLE POSITION>

Note:

Parties shall ensure that, no later than 1 January 2000, diesel fuel

can be marketed within their territory only if it complies with the

environmental specifications set out in Table 9. Where a Party

determines that banning diesel fuel with a sulphur content which

does not comply with the specifications for sulphur content in Table

9, but does not exceed the current content, would raise severe

difficulties for its industries in making the necessary changes in

their manufacturing facilities by 1 January 2000, it may extend the

time period of marketing within its territory until 1 January 2003

at the latest. In such a case the Party shall specify, in a

declaration to be deposited together with its instrument of

ratification, acceptance, approval or accession, that it intends to

extend the time period and present written information on the reason

for this to the Executive Body.

Table 10. Environmental specifications for marketed fuels to be used

for vehicles equipped with positive-ignition engines

Type: Petrol

>TABLE POSITION>

Note:

Parties shall ensure that, no later than 1 January 2005, petrol can

be marketed within their territory only if it complies with the

environmental specifications set out in Table 10. Where a Party

determines that banning petrol with a sulphur content which does not

comply with the specifications for sulphur content in Table 10, but

does comply with Table 8, would raise severe difficulties for its

industries in making the necessary changes in their manufacturing

facilities by 1 January 2005, it may extend the time period of

marketing within its territory until 1 January 2007 at the latest.

In such a case the Party shall specify, in a declaration to be

deposited together with its instrument of ratification, acceptance,

approval or accession, that it intends to extend the time period and

present written information on the reason for this to the Executive

Body.

Table 11. Environmental specifications for marketed fuels to be used

for vehicles equipped with compression-ignition engines

Type: Diesel fuel

>TABLE POSITION>

Note:

Parties shall ensure that, no later than 1 January 2005, diesel fuel

can be marketed within their territory only if it complies with the

environmental specifications set out in Table 11. Where a Party

determines that banning diesel fuel with a sulphur content which

does not comply with the specifications for sulphur content in Table

11, but does comply with Table 9, would raise severe difficulties

for its industries in making the necessary changes in their

manufacturing facilities by 1 January 2005, it may extend the time

period of marketing within its territory until 1 January 2007 at the

latest. In such a case the Party shall specify, in a declaration to

be deposited together with its instrument of ratification,

acceptance, approval or accession, that it intends to extend the

time period and present written information on the reason for this

to the Executive Body.

B. Canada

9. New vehicle emission standards for light-duty vehicles,

light-duty trucks, heavy-duty vehicles, heavy-duty engines and

motorcycles: Motor Vehicle Safety Act (and successor legislation),

Schedule V of the Motor Vehicle Safety Regulations: Vehicle

Emissions (Standard 1100), SOR/97-376, (28 July, 1997), as amended

from time to time.

10. Canadian Environmental Protection Act, Diesel Fuel Regulations,

SOR/97-110 (4 February 1997, sulphur in diesel fuel), as amended

from time to time.

11. Canadian Environmental Protection Act, Benzene in Gasoline

Regulations, SOR/97-493 (6 November 1997), as amended from time to

time.

12. Canadian Environmental Protection Act, Sulphur in Gasoline

Regulations, Canada Gazette, Part II, June 4 1999, as amended from

time to time.

C. United States of America

13. Implementation of a mobile source emission control programme for

light-duty vehicles, light-duty trucks, heavy-duty trucks and fuels

to the extent required by sections 202(a), 202(g) and 202(h) of the

Clean Air Act, as implemented through:

(a) 40 Code of Federal Regulations (C.F.R.) Part 80, Subpart D -

Reformulated Gasoline;

(b) 40 C.F.R. Part 86, Subpart A - General Provisions for Emission

Regulations;

(c) 40 C.F.R. Part 80, section 80.29 - Controls and Prohibitions on

Diesel Fuel Quality.

 

 

ANNEX IX

 

MEASURES FOR THE CONTROL OF EMISSIONS OF AMMONIA FROM AGRICULTURAL

SOURCES

1. The Parties that are subject to obligations in Article 3(8)(a),

shall take the measures set out in this Annex.

2. Each Party shall take due account of the need to reduce losses

from the whole nitrogen cycle.

A. Advisory code of good agricultural practice

3. Within one year from the date of entry into force of the present

Protocol for it, a Party shall establish, publish and disseminate an

advisory code of good agricultural practice to control ammonia

emissions. The code shall take into account the specific conditions

within the territory of the Party and shall include provisions on:

- nitrogen management, taking account of the whole nitrogen cycle,

- livestock feeding strategies,

- low-emission manure-spreading techniques,

- low-emission manure-storage systems,

- low-emission animal housing systems,

- possibilities for limiting ammonia emissions from the use of

mineral fertilisers.

Parties should give a title to the code with a view to avoiding

confusion with other codes of guidance.

B. Urea and ammonium carbonate fertilisers

4. Within one year from the date of entry into force of the present

Protocol for it, a Party shall take such steps as are feasible to

limit ammonia emissions from the use of solid fertilisers based on

urea.

5. Within one year from the date of entry into force of the present

Protocol for it, a Party shall prohibit the use of ammonium

carbonate fertilisers.

C. Manure application

6. Each Party shall ensure that low-emission slurry application

techniques (as listed in guidance document V adopted by the

Executive Body at its seventeenth session (Decision 1999/1) and any

amendments thereto) that have been shown to reduce emissions by at

least 30 % compared to the reference specified in that guidance

document are used as far as the Party in question considers them

applicable, taking account of local soil and geomorphological

conditions, slurry type and farm structure. The timescales for the

application of these measures shall be: 31 December 2009 for Parties

with economies in transition and 31 December 2007 for other

Parties(1).

7. Within one year from the date of entry into force of the present

Protocol for it, a Party shall ensure that solid manure applied to

land to be ploughed shall be incorporated within at least 24 hours

of spreading as far as it considers this measure applicable, taking

account of local soil and geomorphological conditions and farm

structure.

D. Manure storage

8. Within one year from the date of entry into force of the present

Protocol for it, a Party shall use for new slurry stores on large

pig and poultry farms of 2000 fattening pigs or 750 sows or 40000

poultry, low-emission storage systems or techniques that have been

shown to reduce emissions by 40 % or more compared to the reference

(as listed in the guidance document referred to in paragraph (6)),

or other systems or techniques with a demonstrably equivalent

efficiency(2).

9. For existing slurry stores on large pig and poultry farms of 2000

fattening pigs or 750 sows or 40000 poultry, a Party shall achieve

emission reductions of 40 % in s ofar as the Party considers the

necessary techniques to be technically and economically feasible(3).

The timescales for the application of these measures shall be: 31

December 2009 for Parties with economies in transition and 31

December 2007 for all other Parties(4).

E. Animal housing

10. Within one year from the date of entry into force of the present

Protocol for it, a Party shall use, for new animal housing on large

pig and poultry farms of 2000 fattening pigs or 750 sows or 40000

poultry, housing systems which have been shown to reduce emissions

by 20 % or more compared to the reference (as listed in the guidance

document referred to in paragraph (6)), or other systems or

techniques with a demonstrably equivalent efficiency(5).

Applicability may be limited for animal welfare reasons, for

instance in straw-based systems for pigs and aviary and free-range

systems for poultry.

 

(1) For the purpose of the present Annex, "a country with an economy

in transition" means a Party that has made with its instrument of

ratification, acceptance, approval or accession a declaration that

it wishes to be treated as a country with an economy in transition

for the purposes of paragraphs (6) and/or (9) of this Annex.

(2) Where a Party judges that other systems or techniques with a

demonstrably equivalent efficiency can be used for manure storage

and animal housing in order to comply with paragraphs (8) and (10),

or where a Party judges the reduction of emissions from manure

storage required under paragraph (9) not to be technically or

economically feasible, documentation to this effect shall be

reported in accordance with Article (7)(1)(a).

(3) Where a Party judges that other systems or techniques with a

demonstrably equivalent efficiency can be used for manure storage

and animal housing in order to comply with paragraphs (8) and (10),

or where a Party judges the reduction of emissions from manure

storage required under paragraph (9) not to be technically or

economically feasible, documentation to this effect shall be

reported in accordance with Article (7)(1)(a).

(4) For the purpose of the present Annex, "a country with an economy

in transition" means a Party that has made with its instrument of

ratification, acceptance, approval or accession a declaration that

it wishes to be treated as a country with an economy in transition

for the purposes of paragraphs (6) and/or (9) of this Annex.

(5) Where a Party judges that other systems or techniques with a

demonstrably equivalent efficiency can be used for manure storage

and animal housing in order to comply with paragraphs (8) and (10),

or where a Party judges the reduction of emissions from manure

storage required under paragraph (9) not to be technically or

economically feasible, documentation to this effect shall be

reported in accordance with Article (7)(1)(a).