United Nations Environment Programme
Transcription
United Nations Environment Programme
UNITED NATIONS EP Distr. GENERAL United Nations Environment Programme UNEP/POPS/EGB.3/INF/3 27 July 2004 ENGLISH ONLY EXPERT GROUP ON BEST AVAILABLE TECHNIQUES AND BEST ENVIRONMENTAL PRACTICES Third session Tokyo, Japan, 11– 16 October 2004 Item 3 of the provisional agenda1 Development of guidelines on best available techniques and provisional guidance on best environmental practices relevant to the provisions of Article 5 and Annex C of the Stockholm Convention on Persistent Organic Pollutants SUBMISSIONS RECEIVED IN RESPONSE TO SECRETARIAT INVITATION OF 16 APRIL 2004 TO PROVIDE COMMENTS ON THE DRAFT GUIDELINES AND GUIDANCE2 Note by the Secretariat 1. At its second session held in Villarrica, Chile, from 8 to 12 December 2003, the Expert Group to develop guidelines on best available techniques and provisional guidance on best environmental practices relevant to the provisions of Article 5 and Annex C of the Stockholm Convention on Persistent Organic Pollutants agreed to undertake intersessional work to prepare the draft guidance and guidelines for its further consideration at its third session be be held from 11 to 16 October 2004 in Japan. The schedule agreed for the intersessional work that can be found in paragraph 61 of UNEP/POPS/EGB.2/3 which is available at: www.pops.int/ documents/ meetings/bat_bep/2nd_session/egb2_followup. 2. A preliminary draft of the guidance and guidelines was completed on 15 April 2005. On 16 April 2004 the Secretariat transmitted a letter inviting comments on the draft to Stockholm Convention Focal Points, UNEP Official Contact Points and heads of delegations that were present at the seventh session of the Intergovernmental Negotiating Committee for an International Legally Binding Instrument for International Action on Certain Persistent Organic Pollutants. The invitation letter and the draft were also posted on the Stockholm Convention website: www.pops.int. The list of those submitting comments, what they commented on and the full submissions are contained in the annex to the present note. 1 2 UNEP/POPS/EGB.3/1. This document has not been formally edited. For reasons of economy, this document is printed in a limited number. Delegates are kindly requested to bring their copies to meetings and not to request additional copies. Annex Submissions received by the Secretariat of the Stockholm Convention on the draft guidelines on BAT and guidance on BEP Submissions by Governments COUNTRY Botswana OBSERVATIONS Comments on open burning, municipal waste incineration, and medical waste incineration. General comments. General comments. Comments on waste incinerators: municipal and hazardous waste and sewage sludge, cement kilns, production of pulp, sinter plants in the iron industry, open burning, secondary lead production, and chemical production processes. Acknowledged receiving request for comments. Comments on Leather dying, chemical production processes, open burning of wastes, residential combustion sources, firing installations. General comments. General comments and comments on Sections: V.A.1, V.A.2, and V.C. Has no comment. General comments on Section V.A.2 and on the need to keep in mind through out the guidance socio-economic considerations . General comments. General comments. General comments Comments on: production of pulp, open burning, Cement kilns, medical waste and municipal incinerators Comments on Sections V.D., VI.B, V.C., and VI.A. Brazil China Colombia Gabon Germany Italy Japan Jordan Mexico Peru Philippines Slovakia Trinidad and Tobago United States of America Submissions by Members of the Expert Group EXPERTS Algeria Canada Kazakhstan Switzerland UNEP OBSERVATIONS Comments on open burning. Comments on sections: V.A.1, VI.C, VI.E, and V.C. Comments on open burning. Comments on Sections: V.A.1, V.B., and VI.C. General comments and comments on Sections on alternatives, residential combustion sources, firing installations for wood and other biomass Submissions by NGOs ORGANIZATION American Forest & Paper Association Arnika Association – Toxics and Waste Programme Canadian Steel Producers Association Cancer Action Finnish Forest Industries GAIA: Global Alliance for Incineration Alternatives Greenpeace International OBSERVATIONS Comments on Pulp and paper General comments and comments on incineration and cement kilns. General comments Comments on open burning and on incineration Comments on Guidelines on BAT for production of pulp using elemental chlorine General comments on consideration of use of alternative non-combustion processes Comments on sections on consideration of alternatives, V.A.1, VI.A, VI.F Compilation of Comments on the draft guidelines on BAT and guidance on BEP received by the Secretariat of the Stockholm Convention Comments submitted by Governments COMMENTS SUBMITTED BY BOTSWANA Guidelines on open burning • Residues from Agricultural undertakings to be shredded and composted instead of burning in open air. This will facilitate the reduction in the level of dioxins and furans released in to the atmosphere. • Controlled composting in a secured area where soil study has been done to find out how the soil could be useful later (if possible chemicals could be used to facilitate the process of composting). • To develop technology that will facilitate and speed composting especially to enrich the soil for Agricultural purposes in semi arid areas. • Burning of inorganic waste should be totally discouraged. Guidelines on municipal waste • Appropriate and affordable technology for rapid assessment and monitoring of pollutants released from different categories of wastes during incineration. This will facilitate easy monitoring of the level of pollutants. • Improved and approved incinerators to be used. Guidelines on medical waste incineration • Affordable and appropriate technology and guidelines for autoclaving of health care waste should be used. 1 COMMENTS SUBMITTED BY BRAZIL 2 3 COMMENTS SUBMITTED BY CHINA 4 5 6 7 8 9 10 COMMENTS SUBMITTED BY COLOMBIA COMENTARIOS DE COLOMBIA DRAFT GUIDELINES BAT/BEP Section V.A.I: Guidance by source category, Annex C, Part II Source Categories –Waste Incinerators (DRAFT 19/04/04): Municipal and hazardous waste and sewage sludge – Coordinated by Mr. Robert Kellam (United States of America) Colombia está de acuerdo con las mejores técnicas disponibles y las mejores prácticas medioambientales de esta guía, sin embargo, es importante señalar que Colombia no puede sostener económicamente incineradores giratorios dedicados exclusivamente para desechos peligrosos. Por lo anterior, el país ha desarrollado algunas pruebas de coprocesamiento de residuos peligrosos en la producción de cemento con desechos como plásticos y tierras contaminados con plaguicidas y llantas usadas, en hornos giratorios de plantas cementeras colombianas cumpliendo todos los valores limites hasta las Dioxinas/Furanos y PCBs de USEPA y de UE. De otra parte, se propone las siguientes medidas para la minimización de liberaciones de Dioxinas y Furanos en esta categoría: Las estrategias al principio se deben concentrar en las fuentes más generadoras de PCDD/PCDF con el lanzamiento de nuevas y modernas tecnologías de producción, producción más limpia y modernos sistemas de control de polución de emisiones. Se proponen las siguientes medidas acerca de procesos industriales liberadores de PCDD/PCDF, con el fin de reducir las liberaciones de dioxinas y furanos: ¾ Conocer los mecanismos de formación de PCDD/PCDF profundamente en las plantas industriales de esta categoría. Experimentalmente se puede demostrar p.ej en caso de los procesos de combustión que • No solo la combustión directa produce PCDD/PCDF • En la zona de enfriamiento de los gases, como precipitadores electrostáticos, se produce casi 10 veces más PCDD/PCDF. • Los filtros de mangas son mejores que los precipitadores electrostáticos, ya que la temperatura de trabajo puede ser <200°C ó 150°C. Por lo tanto se debe aplicar las mejores técnicas disponibles (BAT). En caso de uso de los precipitadores electroestáticos (ESP) se debe siempre utilizar precipitadores electroestáticos fríos (c-ESP) y jamás precipitadores electroestáticos calientes (hESP), en donde “c-” significa la temperatura de trabajo del equipo de <220°C/150°C y “h-” de > 220°C/150°C • El mismo equipo de control de polución de aire a la temperatura de trabajo de >300°C podría emitir cerca 0,3 ng I-TEQ/Nm3 y a la temperatura de trabajo de <200°C < = 0,1 ng I-TEQ/Nm3 . • Un enfriamiento de choques de los gases de salida por debajo de 200°C reduce la generación de PCDD/PCDF. • Las dioxinas y furanos pueden ser oxidadas a alta temperatura de 800—1200°C ó en un catalizador a temperatura baja. 11 • Las dioxinas y furanos después del filtro de mangas pueden ser reducidas de <0,05 ng/m3 a < 0,01 ng/m3 a través de SCR-—DeDiox catalizador . • Las superficies activas de catalizadores metálicos (Cu, Fe, Ni, Si etc.) en la ceniza volante generando PCDD/PCDF pueden ser bloqueados mediante NH3, H2S ó Aminas. • La ceniza volante impregnada con destructores inorgánicos no volátiles puede reducir 99,99% la concentración generada a la temperatura de 200—400°C por los precursores potenciales indicando que los destructores están envenenando las superficies activas de las cenizas volantes. • Desalienta la incineración de desechos sólidos municipales sus inmensos volúmenes consiguiente su significativo potencial de dar lugar a la liberación de PCDD/PCDF y por Se debe animar la aplicación de las mejores tecnologías disponibles (BAT) y las mejores prácticas medioambientales (BEP) en los procesos de incineración de desechos municipales, peligrosos y lodos de tratamiento de aguas residuales de químicos orgánicos e inorgánicos utilizando filtros de mangas junto con un catalizador a descomponer los PCDD/PCDF ó la combinación de filtro de mangas con inyector de sorbente seco (como carbón activo etc.) cumpliendo el valor limite internacional en emisión al aire de 0.1 ng I-TEQ/Nm3 de PCDD/PCDF. Como un mejor indicador de medidas de mitigación de PCDD/PCDF se debe adecuar y actualizar sucesivamente el inventario básico con base en los datos más precisos y factores de emisión, experimentales de ser posible, más específicos y ajustados a la situación real de cada país, dando una base sustentada para aplicar “National Implementation Plan—NIP” adecuadamente. Además se debe fijar los valores límites de PCDD/PCDF en los residuos/lodos de scrubber/suelos, en el vector agua como el valor existente en el vector aire de 0.1 ng I-TEQ/Nm3. De esta manera se muestra el cumplimiento de los estándares del desempeño (Performance Standards) y del desempeño de reportaje (Performance Reporting). Section V.B.: Guidance by source category, Annex C, Part II Source Categories –Cement kilns firing hazardous waste (Draft 15/04/04) –Coordinated by Ms. Ute Karl (Germany) and Ms. Steffi Richter (Germany) Colombia está de acuerdo con las mejores técnicas disponibles (Best Available Techniques --BAT) y las mejores prácticas medioambientales (Best Environmental Practices--BEP) que esta guía propone para el co - procesamiento de desechos peligrosos in-situ en la producción de cemento. Además, de lo expuesto por la guía Colombia propone las siguientes medidas para la minimización de liberaciones de Dioxinas y Furanos: Las estrategias al principio se deben concentrar en los desechos peligrosos más generadores de PCDD/PCDF con el lanzamiento de nuevas y modernas tecnologías de producción--- producción más limpia—y de modernos sistemas de control de polución de emisiones. Se propone lo siguiente acerca de procesos industriales liberadores de PCDD/PCDF, con el fin de reducir las liberaciones de dioxinas y furanos: ¾ Conocer los mecanismos de formación de PCDD/PCDF profundamente en las plantas industriales de esta categoría. Experimentalmente se puede demostrar p.ej en caso de los procesos de combustión que • No solo la combustión directa produce PCDD/PCDF • En la zona de enfriamiento de los gases, como precipitadores electrostáticos, se produce casi 10 veces más PCDD/PCDF. 12 • Los filtros de mangas son mejores que los precipitadores electrostático, ya que la temperatura de trabajo puede ser < 200°C ó 150°C. Por lo tanto se debe aplicar las mejores técnicas disponibles (BAT). En caso de uso de los precipitadores electroestáticos (ESP) se debe siempre utilizar precipitadores electroestáticos fríos (c-ESP) y jamás precipitadores electroestáticos calientes (hESP), en donde “c-” significa la temperatura de trabajo del equipo de <220°C/150°C y “h-” de > 220°C/150°C • El mismo equipo de control de polución de aire a la temperatura de trabajo de >300°C podría emitir cerca 0,3 ng I-TEQ/Nm3 de PCDD/PCDF y a la temperatura de trabajo de < 200°C < = 0,1 ng I-TEQ/Nm3. • Un enfriamiento de choques de los gases de salida por debajo de 200°C reduce la generación de PCDD/PCDF. Se logra este enfriando Clinker a la temperatura <200°C. • Las dioxinas y furanos pueden ser oxidadas a alta temperatura de 800—1200°C ó en un catalizador a temperatura baja. • Las dioxinas y furanos después del filtro de mangas pueden ser reducidas de <0,05 ng/m3 a < 0,01 ng/m3 a través de SCR-—DeDiox catalizador . • Las superficies activas de catalizadores metálicos (Cu, Fe, Ni, Si etc.) en la ceniza volante generando PCDD/PCDF pueden ser bloqueados mediante NH3, H2S ó Aminas. • La ceniza volante impregnada con destructores inorgánicos no volátiles puede reducir 99,99% la concentración generada a la temperatura de 200—400°C por los precursores potenciales indicando que los destructoresestán envenenando las superficies activas de las cenizas volantes. Se debe animar la aplicación de las mejores tecnologías disponibles (BAT) y las mejores prácticas medioambientales (BEP) en los procesos del co-procesamiento de desechos peligrosos en la producción de cemento, utilizando filtro de mangas junto con un catalizador a descomponer los PCDD/PCDF ó la combinación de filtro de mangas con inyector de sorbente seco (como carbón activo etc.) cumpliendo el valor limite internacional en emisión al aire de 0.1 ng I-TEQ/Nm3 de PCDD/PCDF Como un mejor indicador de medidas de mitigación de PCDD/PCDF se debe adecuar y actualizar sucesivamente el inventario básico con base en los datos más precisos y factores de emisión – experimentales de ser posible--más específicos y ajustados a la situación real del país, dando una base sustentada para aplicar “National Implementation Plan—NIP” adecuadamente. Además se debe fijar los valores límites de PCDD/PCDF en Clinker /Particulas Suspendidas Totales PST/lodos de scrubber y en vector agua (en caso se utiliza Scrubber) como el valor existente en el vector aire de 0.1 ng I-TEQ/Nm3. De esta manera se muestra el cumplimiento de los estándares del desempeño (Performance Standards) y del desempeño de reportaje (Performance Reporting). Section V.C.: Guidance by source category, Annex C, Part II Source Categories–Production of pulp using elemental chlorine or chemicals generating elemental chlorine for bleaching (DRAFT15/04/04)–Coordinated by Ms. Hille Hyytiä (Finland) Colombia está de acuerdo con las mejores técnicas disponibles (Best Available Techniques --BAT) y las mejores prácticas medioambientales (Best Environmental Practices--BEP) de esta guía para la producción de pasta utilizando cloro ó químicos que generan cloro para blanqueado con meta de desligninificación. Además, se propone las siguientes medidas para la minimización de liberaciones de Dioxinas y Furanos en esta categoría: 13 ¾ Las estrategias al principio se debe concentrar en los procesos industriales más generadores de PCDD/PCDF con el lanzamiento de nuevas y modernas tecnologías de producción---producción más limpia—y de modernos sistemas de control de polución de emisiones. Se propone las siguientes medidas acerca de procesos industriales liberadores de 2378-TCDD/TCDF, con el fin de reducir estas liberaciones, tomando en cuenta en primer lugar la realidad del país en cuanto a su tecnología vieja: ¾ Conocer profundamente los mecanismos de formación de 2378-TCDD/TCDF en las plantas industriales de esta categoría. Experimentalmente se puede demostrar que evitando la presencia de PCDD/PCDF precursores como inclorados DBD (Dibenzo-p-dioxin) y DBF (Dibenzofuran) en las formulaciones de ciertos “Defoamers” utilizados mientras del blanqueado con cloro en la industria de producción de pasta y papel se puede eliminar la generación de 2378-TCDD/TCDF en la “C-stage” del proceso. • En la producción de pasta Kraft blanqueada se debe recuperar las fibras en las distintas etapas así evitando la generación de lodos durante el tratamiento de efluentes. • No solo la liberación al aire de PCDD/PCDF a través del quemado del licor negro en el ciclo de recuperación a generar energía y recuperar químicos inorgánicos de proceso, aunque evitando la liberación de cenizas. • En la zona de enfriamiento de los gases, como precipitadores electrostáticos, se produce casi 10 veces más PCDD/PCDF. • Los filtros de mangas son mejores que los precipitadores electrostáticos, ya que la temperatura de trabajo puede ser < 200°C ó 150°C. Por lo tanto se debe aplicar las mejores técnicas disponibles (BAT). En caso de uso de los precipitadores electrostáticos (ESP) se debe siempre utilizar precipitadores electrostáticos fríos (c-ESP) y jamás precipitadores electrostáticos calientes (hESP), en donde “c-” significa la temperatura de trabajo del equipo de < 220°C/150°C y “h-” de > 220°C/150°C. Se recomienda la utilización de filtro de mangas. • El mismo equipo de control de polución de aire a la temperatura de trabajo de > 300°C podría emitir cerca 0,3 ng I-TEQ/Nm3 y a la temperatura de trabajo de < 200°C < = 0,1 ng I-TEQ/Nm3. • Un enfriamiento de choque de los gases de salida por debajo de 200°Creduce la generación de PCDD/PCDF. • Las dioxinas y furanos pueden ser oxidadas a alta temperatura de 800—1200°C ó en un catalizador a temperatura baja. • Las dioxinas y furanos después del filtro de mangas pueden ser reducidas de < 0,05 ng/m3 a < 0,01 ng/m3 a través de SCR-—DeDiox catalizador. • Las superficies activas de catalizadores metálicos (Cu, Fe, Ni, Si etc.) en la ceniza volante generando PCDD/PCDF pueden ser bloqueados mediante NH3, H2S ó Aminas. • La ceniza volante impregnada con destructores inorgánicos no volátiles puede reducir 99,99% la concentración generada a la temperatura de 200—400°C por los precursores potenciales indicando que los destructores están envenenando las superficies activas de las cenizas volantes. Se debe animar la aplicación de las mejores tecnologías disponibles (BAT) y las mejores prácticas medioambientales (BEP) en proceso del quemado del material orgánico en el ciclo de recuperación a generar energía y recuperar químicos inorgánicos de proceso, utilizando filtro de mangas junto con un catalizador a descomponer los PCDD/PCDF ó la combinación de filtro de mangas con inyector de sorbente seco (como carbón activo etc.) cumpliendo el valor limite internacional en emisión al aire de 0.1 ng I-TEQ/Nm3 de PCDD/PCDF. 14 Como un mejor indicador de medidas de mitigación de PCDD/PCDF se debe adecuar y actualizar sucesivamente el inventario básico con base en los datos más precisos y factores de emisión, experimentales de ser posible, más específicos y ajustados a la situación real de cada país, dando una base sustentada para aplicar el “National Implementation Plan—NIP” adecuadamente. Además se deben fijar los valores límites de PCDD/PCDF en Productos/Residuos/Particulas Suspendidas Totales PST/lodos de scrubber y en vector agua (en caso se utiliza Scrubber) como el valor existente en el vector aire de 0.1 ng I-TEQ/Nm3. De esta manera se muestra el cumplimiento de los estándares del desempeño (Performance Standards) y del desempeño de reportaje (Performance Reporting). Section V.D.2: Guidance by source category, Annex C, Part II Source Categories –Sinter plants in the iron industry (DRAFT 22/04/04) –Coordinated by Mr. Patrick Finlay (Canada) Colombia está de acuerdo con las mejores técnicas disponibles (Best Available Techniques --BAT) y las mejores prácticas medioambientales (Best Environmental Practices--BEP) de esta guía para las plantas de sinterización en la industria de hierro. Además Colombia propone las siguientes medidas para la minimización de liberaciones de Dioxinas y Furanos en esta categoría: ¾ Las estrategias al principio se deben concentrar en procesos industriales más generadoras de PCDD/PCDF con el lanzamiento de nuevas y modernas tecnologías de producción, producción más limpia, y de modernos sistemas de control de polución de emisiones. Se propone las siguientes medidas acerca de procesos industriales liberadores de PCDD/PCDF, con el fin de reducir las liberaciones de dioxinas y furanos, tomando en cuenta en primer lugar la realidad del país en cuanto a su tecnología vieja: ¾ Conocer los mecanismos de formación de PCDD/PCDF profundamente en las plantas industriales de esta categoría. Experimentalmente se puede demostrar p.e., en caso del proceso de sinterización que: • No solo el proceso de sinterización produce PCDD/PCDF • En la zona de enfriamiento de los gases, como precipitadores electrostáticos, se produce casi 10 veces más PCDD/PCDF. • Los filtros de mangas son mejores que los precipitadores electrostáticos, ya que la temperatura de trabajo puede ser < 200°C ó 150°C. Por lo tanto se debe aplicar las mejores técnicas disponibles (BAT). En caso de uso de los precipitadores electroestáticos (ESP) se debe siempre utilizar precipitadores electroestáticos fríos (c-ESP) y jamás precipitadores electroestáticos calientes (hESP), en donde “c-” significa la temperatura de trabajo del equipo de <220°C/150°C y “h-” de >220°C/150°C. Se recomienda la utilización de filtro de mangas. • El mismo equipo de control de polución de aire a la temperatura de trabajo de >300°C podría emitir cerca 0,3 ng I-TEQ/Nm3 y a la temperatura de trabajo de < 200°C < = 0,1 ng I-TEQ/Nm3. • Un enfriamiento de choques de los gases de salida por debajo de 200°Creduce la generación de PCDD/PCDF. • Las dioxinas y furanos pueden ser oxidadas a alta temperatura de 800—1200°C ó en un catalizador a temperatura baja. • Las dioxinas y furanos después del filtro de mangas pueden ser reducidas de <0,05 ng/m3 a <0,01 ng/m3 a través de SCR-—DeDiox catalizador. 15 • Las superficies activas de catalizadores metálicos (Cu, Fe, Ni, Si etc.) en la ceniza volante generando PCDD/PCDF pueden ser bloqueados mediante NH3, H2S ó Aminas. • La ceniza volante impregnada con destructores inorgánicos no volátiles puede reducir 99,99% la concentración generada a la temperatura de 200—400°C por los precursores potenciales indicando que los destructoresestán envenenando las superficies activas de las cenizas volantes. Se debe animar la aplicación de las mejores tecnologías disponibles (BAT) y las mejores prácticas medioambientales (BEP) en las plantas de sinterización en la industria de hierro utilizando filtro de mangas junto con un catalizador a descomponer los PCDD/PCDF ó la combinación de filtro de mangas con inyector de sorbente seco (como carbón activo etc.) cumpliendo el valor limite internacional en emisión al aire de 0.1 ng I-TEQ/Nm3 de PCDD/PCDF Como un mejor indicador de medidas de mitigación de PCDD/PCDF se debe adecuar y actualizar sucesivamente el inventario básico con base en los datos más precisos y factores de emisión – experimentales de ser posible--más específicos y ajustados a la situación real de cada país, dando una base sustentada para aplicar “National Implementation Plan—NIP” adecuadamente. Además se deben fijar los valores límites de PCDD/PCDF en Residuos /Particulas Suspendidas Totales PST/lodos de scrubber y en vector agua (en caso se utiliza Scrubber) como el valor existente en el vector aire de 0.1 ng I-TEQ/Nm3. De esta manera se muestra el cumplimiento de los estándares del desempeño (Performance Standards) y del desempeño de reportaje (Performance Reporting). Section VI.A: Guidance by source category, Annex C, Part III Source Categories –Open burning of wastes (DRAFT 13/04/04)–Coordinated by Mr. Francis Kihumba (Kenya) and Mr. William Carroll (international Council of Chemical Associations) Colombia está de acuerdo con las mejores técnicas disponibles (Best Available Techniques --BAT) y las mejores prácticas medioambientales (Best Environmental Practices--BEP) que esta guía propone. Además se propone las siguientes medidas para la minimización de liberaciones de Dioxinas y Furanos en esta categoría: ¾ Las estrategias al principio se deben concentrar en las fuentes más generadoras de PCDD/PCDF con el lanzamiento de nuevas y modernas tecnologías de producción---producción más limpia—y de modernos sistemas de control de polución de emisiones. Se proponen las siguientes medidas acerca de las quemas abiertas con el fin de reducir las liberaciones de dioxinas y furanos, tomando en cuenta en primer lugar la realidad del país en cuanto a su tecnología vieja: 1. Conocer profundamente los mecanismos de formación de PCDD/PCDF de esta categoría de desechos de quemas a cielo abierto. • Las quemas a cielo abierto liberan PCDD/PCDF, HCB, PCBs, HAPs, PST, Benceno y CO. Según el Decreto 948/95 de Colombia, se prohiben este tipo de quemas; sin embargo, por falta del seguimiento de las autoridades ambientales se siguen realizando quemas a cielo abierto. Las quemas a cielo abierto son una mala practica. Por lo tanto y de acuerdo con lo planteado por la guía, el enfoque de la implementación del Convenio de Estocolmo debe ser el de buscar alternativas a las quemas abiertas y no el de ensayar mejorar una mala práctica. 2. Prevenir los quemados incontrolados abiertos al cielo de residuos agrícolas (cáscara de arroz, bagazo de caña etc.), para la reclamación térmica de cobre de alambre (quemas abiertas) y de desechos sólidos municipales. Cáscara de arroz p.ej. se puede utilizar en la producción de papel, 16 su procesamiento al “charcoal vineger” como pesticidas naturales evitando la dependencia de los pesticidas con base en química y además como materiales para “Mulching and soil amendment for organic farming”. Se debe animar la aplicación de las mejores tecnologías disponibles (BAT) y las mejores prácticas medioambientales (BEP) para el quemado y no permitir quemas a cielo abierto. Como un mejor indicador de medidas de mitigación de PCDD/PCDF se debe adecuar y actualizar sucesivamente el inventario básico con base en los datos más precisos y factores de emisión – experimentales de ser posible--más específicos y ajustados a la situación real de cada país, dando una base sustentada para aplicar “National Implementation Plan—NIP” adecuadamente. Además se debe ensayar fijar el valor límite de PCDD/PCDF en immisión (calidad del aire) alrededor de las quemas a cielo abierto. Section VI.B.I : Guidance by source category, Annex C, Part III Source Categories – Secondary lead production (DRAFT 22/04/04) –Coordinated by Mr. Patrick Finlay (Canada) Colombia está de acuerdo con las mejores técnicas disponibles (Best Available Techniques--BAT) y las mejores prácticas medioambientales (Best Environmental Practices--BEP) de esta guía para la producción secundaria de plomo. Además se propone las siguientes medidas para la minimización de liberaciones de Dioxinas y Furanos en esta categoría: Las estrategias al principio se deben concentrar en procesos industriales más generadoras de PCDD/PCDF con el lanzamiento de nuevas modernas tecnologías de producción, producción más limpia, y de modernos sistemas de control de polución de emisiones. Se propone las siguientes medidas acerca de procesos industriales liberadores de PCDD/PCDF, con el fin de reducir las liberaciones de dioxinas y furanos: ¾ Conocer profundamente los mecanismos de formación de PCDD/PCDF en las plantas industriales de esta categoría. Experimentalmente se puede demostrar p.ej en caso de los procesos de fundición que • No solo la fundición directa produce PCDD/PCDF • En la zona de enfriamiento de los gases, como precipitadores electrostáticos, se produce casi 10 veces más PCDD/PCDF. • Los filtros de mangas son mejores que los precipitadores electrostáticos, ya que la temperatura de trabajo puede ser < 200°C ó 150°C. Por lo tanto se debe aplicar las mejores técnicas disponibles (BAT). En caso de uso de los precipitadores electrostáticos (ESP) se debe siempre utilizar precipitadores electrostáticos fríos (c-ESP) y jamás precipitadores electrostáticos calientes (hESP), en donde “c-” significa la temperatura de trabajo del equipo de <220°C/150°C y “h-” de >220°C/150°C. Se recomienda la utilización de filtro de mangas. • El mismo equipo de control de polución de aire a la temperatura de trabajo de >300°C podría emitir cerca 0,3 ng I-TEQ/Nm3 y a la temperatura de trabajo de <200°C < = 0,1 ng I-TEQ/Nm3. • Un enfriamiento de choques de los gases de salida por debajo de 200°Creduce la generación de PCDD/PCDF. • Las dioxinas y furanos pueden ser oxidadas a alta temperatura de 800—1200°C ó en un catalizador a temperatura baja. 17 • Las dioxinas y furanos después del filtro de mangas pueden ser reducidas de <0,05 ng/m3 a < 0,01 ng/m3 a través de SCR-—DeDiox catalizador . • Las superficies activas de catalizadores metálicos (Cu, Fe, Ni, Si etc.) en la ceniza volante generando PCDD/PCDF pueden ser bloqueados mediante NH3, H2S ó Aminas. • La ceniza volante impregnada con destructores inorgánicos no volátiles puede reducir 99,99% la concentración generada a la temperatura de 200—400°C por los precursores potenciales indicando que los destructores están envenenando las superficies activas de las cenizas volantes. Se debe animar la aplicación de las mejores tecnologías disponibles (BAT) y las mejores prácticas medioambientales (BEP) en la producción secundaria de plomo utilizando filtro de mangas junto con un catalizador a descomponer los PCDD/PCDF ó la combinación de filtro de mangas con inyector de sorbente seco (como carbón activo etc.) cumpliendo el valor limite internacional en emisión al aire de 0.1 ng I-TEQ/Nm3 de PCDD/PCDF Como un mejor indicador de medidas de mitigación de PCDD/PCDF se debe adecuar y actualizar sucesivamente el inventario básico con base en los datos más precisos y factores de emisión, experimentales de ser posible, más específicos y ajustados a la situación real de cada país, dando una base sustentada para aplicar “National Implementation Plan—NIP” adecuadamente. Además se deben fijar los valores límites de PCDD/PCDF en Residuos /Particulas Suspendidas Totales PST/lodos de scrubber y en vector agua (en caso se utiliza Scrubber) como el valor existente en el vector aire de 0.1 ng I-TEQ/Nm3. De esta manera se muestra el cumplimiento de los estándares del desempeño (Performance Standards) y del desempeño de reportaje (Performance Reporting). Section VI.F: Guidance by source category, Annex C, Part III Source Categories –Chemical production processes (DRAFT 13/04/04) –Coordinated by Mr. William Carroll (international Council of Chemical Associations) Colombia está de acuerdo con las mejores técnicas disponibles (Best Available Techniques -BAT) y las mejores prácticas medioambientales (Best Environmental Practices--BEP) de esta guía. Además se propone las siguientes medidas para la minimización de liberaciones de Dioxinas y Furanos en esta categoría: ¾ Las estrategias al principio se deben concentrar en las fuentes más generadoras de PCDD/PCDF con el lanzamiento de nuevas y modernas tecnologías de producción--producción más limpia—y de modernos sistemas de control de polución de emisiones. Se proponen las siguientes medidas acerca de procesos de producción de químicos con el fin de reducir las liberaciones de dioxinas y furanos: ¾ Conocer profundamente los mecanismos de formación de PCDD/PCDF en las plantas productoras de químicos en esta categoría. Experimentalmente se puede demostrar p.ej en el caso de la destrucción térmica de los productos subsidiarios durante de los procesos de producción de químicos orgánicos y inorgánicos que: • No solo destrucción directa produce PCDD/PCDF • En la zona de enfriamiento de los gases, como precipitadores electrostáticos, se produce casi 10 veces más PCDD/PCDF. • Los filtros de mangas son mejores que los precipitadores electrostático, ya que la temperatura de trabajo puede ser <200°C ó 150°C. Por lo tanto se debe aplicar las mejores técnicas disponibles 18 (BAT). En caso de uso de los precipitadores electroestáticos (ESP) se debe siempre utilizar precipitadores electroestáticos fríos (c-ESP) y jamás precipitadores electroestáticos calientes (hESP), en donde “c-” significa la temperatura de trabajo del equipo de <220°C/150°C y “h-” de >220°C/150°C • El mismo equipo de control de polución de aire a la temperatura de trabajo de >300°C podría emitir cerca 0,3 ng I-TEQ/Nm3 de PCDD/PCDF y a la temperatura de trabajo de < 200°C < = 0,1 ng I-TEQ/Nm3. • Un enfriamiento de choques de los gases de salida por debajo de 200°C reduce la generación de PCDD/PCDF. • Las dioxinas y furanos pueden ser oxidadas a alta temperatura de 800—1200°C ó en un catalizador a temperatura baja. • Las dioxinas y furanos después del filtro de mangas pueden ser reducidas de <0,05 ng/m3 a < 0,01 ng/m3 a través de SCR-—DeDiox catalizador. • Las superficies activas de catalizadores metálicos (Cu, Fe, Ni, Si etc.) en la ceniza volante generando PCDD/PCDF pueden ser bloqueados mediante NH3, H2S ó Aminas. • La ceniza volante impregnada con destructores inorgánicos no volátiles puede reducir 99,99% la concentración generada a la temperatura de 200—400°C por los precursores potenciales indicando que los destructores están envenenando las superficies activas de las cenizas volantes. Se debe animar la aplicación de las mejores tecnologías disponibles (BAT) y las mejores prácticas medioambientales (BEP) p.ej. en la industria de cloro, destrucción térmica de los productos subsidiarios en los procesos de producción de químicos orgánicos y inorgánicos utilizando filtro de mangas junto con un catalizador a descomponer los PCDD/PCDF ó la combinación de filtro de mangas con inyector de sorbente seco (como carbón activo etc.) cumpliendo el valor limite internacional en emisión al aire de 0.1 ng I-TEQ/Nm3 de PCDD/PCDF Como un mejor indicador de medidas de mitigación de PCDD/PCDF se debe adecuar y actualizar sucesivamente el inventario básico con base en los datos más precisos y factores de emisión, experimentales de ser posible, más específicos y ajustados a la situación real del país, dando una base sustentada para aplicar “National Implementation Plan—NIP” adecuadamente. Además se debe fijar los valores límites de PCDD/PCDF en los residuos/productos subsidiarios, en el vector agua y en químicos principales producidos como el valor existente en el vector aire de 0.1 ng I-TEQ/Nm3. Estos químicos producidos con trazas de PCDD/PCDF se deben registrar en un Inventario de Liberación de Sustancias Tóxicas como el que existe en EE.UU –denominado TRI (Toxics Release Inventory) y también en Alemania. De esta manera se muestra el cumplimiento de los estándares del desempeño (Performance Standards) y del desempeño de reportaje (Performance Reporting). 19 COMMENTS SUBMITTED BY GABON 20 COMMENTS SUBMITTED BY GERMANY Federal Environmental Agency Berlin, 18.06.2004 German comments to the Draft guidelines on best available techniques (BAT) and guidance on best environmental practices (BEP) relevant to Article 5 and Annex C of the Stockholm Convention on Persistent Organic Pollutants The draft guidelines on best available techniques and guidance on best environmental practices relevant to Article 5 and Annex C of the Stockholm Convention on Persistent Organic Pollutants are valuable documents for giving countries information how to eliminate and restrict as most as possible PCDD/F releases from different source categories. From our site was noted, that these guidances could for developed and developing countries as well a sophisticated basis to be applied in a flexible manner. The Federal Environmental Agency can give comments to the following source categories: - Leather dyeing and finishing - Chemical production process - Open burning of wastes - Residential combustion sources - Firing installations for wood and other biomass fuels Leather dyeing and finishing As outlined in the Draft Guideline - the occurrence of PCDD/PCDF in the textile and leather industries are due to the use of chlorinated chemicals, esp. PCP, to protect and conserve the raw – material. Available substitutes for preservation should be outlined in the Guidance. The following substitutes are used in Germany since the national phasing out of PCP: 2-Thiocyanatomethylthiobenzothiazole (TCMTB) - o-Phenylphenole (oPP) - 4-Chloro-3-methyl-phenole (CMK) - 2-Octylisothiazolinone (OIT) The mentioned chemicals are assessed as less hazardous for the environment than PCP, but not as inherently safe at all. Chemical production processes There are some minor comments to the guidance, which are included in the text with comments in the context of the relevant chapters. The changes are colored: 1.4.1 Fixed Bed Oxychlorination. Fixed bed reactors resemble multi-tube heat exchangers, with the catalyst packed in vertical tubes held in a tubesheet at top and bottom. 21 Uniform packing of catalyst within the tubes is important to ensure uniform pressure drop, flow, and residence time through each tube. Reaction heat is removed by generating steam on the shell side of the reactor, or by flowing some other heat transfer fluid through it. Temperature control in these reactions is important. The tendency to develop hot spots in a fixed bed can be minimized by packing the reactor tubes with active catalyst and inert diluent mixtures in proportions that vary along the length of the tubes, so that there is low catalyst activity at the inlet, but the activity steadily increases to a maximum at the outlet. Alternatively, tubes can be packed with catalyst formulated to have an activity gradient along the length of the tubes. Multiple reactors in series can also be used in fixed bed oxychlorination, providing a similar activity gradient. Using pure oxygen as feed instead of air permits lower temperature operation and therefore lowers the formation of chlorinated byproducts. However this must be balanced against the cost of energy expended in producing pure oxygen. 6 Staging the air or oxygen feed and grading the catalyst activity flatten the temperature profile and allow improved temperature control.7 1.5 Main Product Isolation. Another common facet of these processes is the need to purify products that will either be sold or used in subsequent process steps. In virtually all cases, organic reaction products will be distilled. Fractional distillation separates streams of desired products and also separates desired product from unwanted high molecular weight materials called “heavy ends” or tars. In the European Union the Integrated Pollution Prevention and Control (IPPC) Directive requires the use of Best Available Techniques (BAT) in generating a plant permit. To facilitate this, BAT Reference Documents (BREFs) are produced under the Directive by the European Integrated Pollution Prevention and Control Bureau (EIPPCB). Several of these are relevant to the application of BAT to processes using chlorination. For example, the BREF relating to Large Volume Organic Chemical Processes produced under the IPPC Directive contains discussion of distillation.6 1.6 By-product Destruction. Undesired materials, including heavy ends are destroyed in thermal processes, with or without oxygen. Figure 4 shows a prototypical heavy ends destruction train with HCl recovery. When there are air, water and solid emissions from these processes, these streams can be analyzed and treated for by-product POPs contamination. In many Countries treatment systems are well-defined by regulation. Further information are available in the BREFs on Large Volume Organic Chemical Processes the and on Treatment of Water and Gas Outputs from the Chemical Sector. 4.1.1 Distillation and Internal Recycling of By-products. Distillation is used primarily to produce product of a purity appropriate to downstream processing. As an example, VCM is manufactured via oxychlorination and purified by distillation. Rigorous distillation is used due to the potential for disruption of subsequent polymerization process by impurities. Unsaturated materials that might act as co-monomers competing in the polymerization and saturated or aromatic materials susceptible to free radical reactions other than polymerization can negatively impact polymerization reaction kinetics. Distillation and high purity are important for good production. Distillation systems can be designed to effect separation of materials of closely- or widely-separated boiling points. The boiling points of chemical products of direct chlorination and the boiling points of competing impurities allow for their practical separation. Their boiling points are also sufficiently different from those of the unintended POPs, however, that virtually complete separation can 22 be accomplished. The Large Volume Organic BREF notes that purified EDC does not contain significant amounts of PCDD/F.6 Destruction of chlorinated by-product materials allows for HCl to be harvested and reused.14 This is deemed “greater impact” because small changes in POPs generation upstream of distillation are not reflected in the quality of desired products after distillation. Distillation is a means of separating the desired product from inadvertend sideproducts used across the chemical production industry from commodities of pesticides. Adapting the design and operation of distillation apparatus is, in principle, relatively straightforward. Residual side product contained in commercial product can be minimized by appropriate design and operation of the distillation apparatus. Effecting more complete separation for materials with boiling points that are not so widely separated as, for example, those of vinyl chloride and the various lower molecular weight side products is for the most part a matter of correct design and construction and operation cost. Differences in concentration of residual byproduct POPs in commercial product may be due to differences in local regulation of products. 4.1.5 Modified Production Pentachlorophenate. of Pentachlorophenol (PCP) and Sodium The following processes are also described in the Toolkit.2 Three routes to PCP are known commercially. Chlorination of phenol by Cl2 over a catalyst, hydrolysis of hexachlorobenzene (HCB) with sodium hydroxide and thermolysis of HCB. The most common route today is the first. Sodium pentachlorophenate can be produced via hydrolysis of HCB, or more commonly, by treatment of PCP by sodium hydroxide. For both products, careful control of reaction conditions (e.g., temperature, chlorine feed rate and purity of catalyst) leads to significant reductions of dioxin microcontaminants. In the US, emission of these materials was reduced from ca 3-4 mg I-TEQ/kg in the mid- to late-1980s to ca 1 mg I-TEQ/kg in the years since 1988 .3 Further information referring PCDD/F-emissions from the chlorine process of titanium dioxid production: There is one plant in Germany, which is performing this type of process (Kronos Titan, Leverkusen). Measurements gave no information of considerable emissions of PCDD/F, at least they are quite below 0,1 ng TE/m3. Open burning of wastes A very helpful draft guidance. Our observation is, that in the context of open burning of wastes more or less measures under Best Environmental Practices (BEP) are more relevant, than those under Best Available Techniques (BAT). This guidance seems to be a quite good example, were BEP – measures could be given priority, or falling under BEP anyway. 23 Residential combustion sources For this draft guidance some comments should be taken into account, with the excuse at the other hand, that for some of them no direct proposal for reviewing is connected. These comments are: • The issue is very difficult and quite complex, as various background conditions are to be considered. But in spite of this fact the scope of the source category should be outlined. This should include a short description, if only households or smaller and medium heating systems should be touched as far as possible connected to a performance range. • The introduction (No. 1.0) presents some very general information about emissions for PCB, HCB and PCDD/F from residential combustion sources. We would like to propose, that any data should be used together with a quotation only and by giving the literature to make them transparently. This relates especially also to tables 1 to 3. It should be also pointed out, that emission data in this context need some background information. For PCB and HCB - as far as we are informed - currently no confidential data are available. From Germany at least, we have regrettably also no reliable data to add. Possibly such data – especially if they are not very reliable - are not needed to a big extend at this stage, as applicable measures should be in the focus of this guidance. But in any case of giving data – these should quoted thoroughly. • The draft guidance is outlining measures in a very general way in many cases. A more descriptive outline of techniques for basic combustion types using oil, natural gas and solid fuels should be added. A differentiation between single and central heating systems should be also included. Having in mind and in spite of the fact, that this guidance will be a big issue especially for developing countries, where simple measures of BEP may be of prior interest, some examples of modern combustion techniques with BAT, used in developed countries should be given. • Under No. 4.2 an information for developing countries is given, that the combustion of plastics in heating systems is occuring. We would propose to delete such any hint, as such a practice is and should be forbidden (deletion of the sentence: “Unfortunately, in developed countries people use plastics as fuel.”) • The opportunity to use regenerative energies (e.g. solar) should be mentioned in the context of residential heating under "further recommendations" (No. 5.0) as alternative to classical "residential combustion". Firing installations for wood and other biomass fuels This paper will be helpful, but no specific focus on the requirements of developing countries can be identified. Some comments to this paper: • Combustion of other biomass, than wood, seems to be a bit little underrepresented. It should be incorporated the information, that combustion of straw, cereals, grass and other grassy material is causing considerably higher PCDD/F – emissions, than combustion of untreated wood. 24 • In the context of descriptions for techniques for PCDD/F-reduction, only techniques to be applicable at bigger non-residential combustion devices are outlined. Some of these measures are only be used (e.g. SCR) in Germany in the case of combustion of treated wood. The application of effective dust precipitators should be given focus, as most PCDD/F are adsorbed at particles. • A huge proportion of PCDD/F – emissions in Germany is emitted from residential combustion devices (in the context, that industrial sources have been reduced to a very large extend during the years). This means, that focus should be given sources of the type of residential combustion. Simple an applicable primary measures according BEP for households are primary needed. So chapter 3 and 6 should include guidance for adequate use of heating systems. Those includes: No co-incineration of wastes (already in chapter 6), Requirement to use licensed, higher-qualitatively fuels (no use of wet and treated wood at all), periodically service for heating systems, stepwise substitution of old potentially high-emission systems, where implementable by modern systems (pelleticed wood combustion, vessels with buffer saving systems). 25 COMMENTS SUBMITTED BY ITALY ITALIAN COMMENTS ON DRAFT GUIDELINES ON BEST AVAILABLE TECHNIQUES AND GUIDANCE ON BEST ENVIRONMENTAL PRACTICES RELEVANT TO ARTICLE 5 AND ANNEX C OF THE STOCKHOLM CONVENTION Italy would like to thank the Executive Secretary, Mr. James B. Willis, for inviting Governments and other relevant organisations to provide comments on the Draft Guidelines on Best Available Techniques and Guidance on Best Environmental Practices, developed by the Expert Group on BAT and BEP. All the 23 documents available up to now are very valuable, and we wish to thank Experts that made a lot of work to perform them in due time. Moreover, we appreciate the choice to include in various sections relevant information taken from BAT reference documents, produced under the information exchange provisions, contained in article 16 (2) of the European Union Directive on Integrated Pollution Prevention and Control. As a general comment, we would like only to suggest to harmonise all the contributions at the end of the process in the final draft to be presented at COP1. In effect, some little differences arise reading the texts: for instance, some sections give an idea about costs of the described techniques, while others do not refer to this aspect. Another characteristic not always mentioned is the achievable reduction level associated with the adoption of the techniques, or their applicability to new and/or existing plants. From our point of view, these information are useful and should not be missed, because their knowledge helps to evaluate the best solution. Some sections make a clear distinction between BAT and BEP, while in others the two are mixed: this may ingenerate confusion in the reader and in the final user of the document. The mandate of the Expert Group is to develop guidelines on best available techniques and to develop provisional guidance on best environmental practices relevant to the provisions of article 5 of the Convention, for consideration by the Conference of the Parties upon entry into force of the Convention (see document UNEP/POPS/INC6/22, Annex VII: “Terms of reference for the Expert Group on Best Available Techniques/Best Environmental Practices”). During the EGB1 meeting it was recognised that BEP is a more overarching notion that might include policies and strategies, while BAT is well defined and conceptually developed in the text of the Convention, (see EGB1 meeting report, point 25 and 26). Therefore, we suggest to separate the descriptions of BATs from those of BEPs in all sections, so helping final users of the guidelines and guidance in choosing of the best solutions. The document of Section II, “Consideration of alternatives”, is the only one that has some paragraphs in square brackets. The introductory note of one of the two co-ordinators clarifies the reason why this happened. We are confident that the difference of views among Experts will overcome during the third meeting of the Expert Group, scheduled in Japan next October. 26 COMMENTS SUBMITTED BY JAPAN JAPAN Date: June 23, 2004 Japan’s comments on the Draft guidelines on best available techniques and guidance on best environmental practices relevant to Article 5 and Annex C of the Stockholm Convention on Persistent Organic Pollutants are as follow. General Comments: 1. In current draft guidelines, numerical values such as “Emission Limit Value,” “Achievable Level,” etc., and the measurement data are given as reference information in several parts. However, the following points should be clarified before providing numerical values. First, different measuring methods of PCDD/PCDF are used by countries. Under the circumstance, the same quantity of unintentional PCDD/PCDF emission could be estimated differently according to the measuring method. Therefore, specific conditions under which the numerical values are estimated should be clarified. The second point regards variation of units used by countries. In the guidelines, many units including m3, Rm3, dscm are used. They should be harmonized, for example, by using conversion formulas. 2. Some of the current draft guidelines refer to the release limit values as “Emission Limit Value,” “Achievable Level,” etc.. In order to avoid unnecessary confusion, these expressions should be unified so that it is clear that those levels are referential values. In paragraph 29 of the report of the 2nd session of the Expert Groups on BAT and BEP, it is agreed that the release limit values in guidelines are included as reference information. (See the 2nd session of the Expert Groups on BAT and BEP practices) 3. We would like to provide Japan’s emission standards and effluent standards of dioxins (see attached table). Specific Comments: 4. [Section V. A. 1 Waste Incinerators: Municipal and hazardous waste, and sewage sludge] (Page 8) 3.1 General Incinerator Design, Paragraph 1 With regard to the sentence “Incinerators are designed for full oxidative combustion over a general temperature range of 850-1400ºC.,” we would like to clarify the meaning of “combustion.” In Japan, combustions are categorized according to the temperature under which these combustions are conducted as follows; "-1000ºC: combustion," "1000-1200ºC: calcinations," "1200ºC-: melting." Please instruct us on if the “combustion” in the sentence contradicts with the above categories or not. 5. [Section V. A. 1 Waste Incinerators: Municipal and hazardous waste, and sewage sludge] (Page 13) 3.2.2.3 Refuse-derived fuel, Paragraph 2, 16 The expression ”very large” MWC facilities seems inadequate from Japan’s standard. In Japan, relatively large-scale MWC facilities, including the scale of 30t/16h, are used to incinerate refusederived fuel as it is difficult for small-scale MWC facilities to recover heat efficiently. 6. [Section V. A. 1 Waste Incinerators: Municipal and hazardous waste, and sewage sludge] (Page 35) 6.3.2 Fly Ash and Other Flue Gas Treatment Residue Techniques, Paragraph 12 We propose to amend the sentence into the following: 27 “If the content exceeds the limit, the ash must be stabilized or destruct.” (Reason) Japan possesses a scientific concern that re-incineration of fly ash may discharge undecomposed dioxins. Therefore, re-incineration is not permitted for fly ash treatment in the Waste Management and Public Cleansing Law in Japan. 7. [Section V. A. 2 : Waste Incinerators: Medical Waste] (Page 8) 5. Alternative Techniques Diagram, (APPROPROATE TREATMENT OPTIONS: frame 3) We propose to add the following sentence: Sharps (not infection) Municipal waste incineration (specially adapted for this → purpose) Hazardous waste disposal route(e.g.,sterilization) (Reason) As sterilization is equally effective in treating sharps, sharp wastes are treated in the same manner as infectious wastes under the Infectious Waste Treatment Manual in Japan. Therefore, not only incineration but also sterilization are allowed as a disposal method. 8. [Section V. C : Production of pulp using elemental chlorine or chemicals generating elemental chlorine for bleaching] Our final comment regards Draft Guideline on BAT for production of pulp using elemental chlorine submitted by the secretariat. Due to Japan’s dioxin problems in 1989, oxygen bleaching has been introduced to all bleaching plants. Some of the plants are smoothly converting to ECF and we believe the process will be complete by FY2005. Moreover, most of the technologies mentioned in BAT have already been carried out in Japan. - END Regulations for Emission Gas and Effluent Relating to Dioxins in Japan The control standards for dioxins for the emission gas and effluent have been set in the Law Concerning Special Measures against Dioxins (the Dioxins Law; promulgated on July 16, 1999) at the strictest values achievable at present. Dioxins are defined to include PCDDs, PCDFs and co-planar PCBs in the Dioxins Law. The level of dioxins is expressed as TEQ calculated according to WHO-TEF(1998). 1) Emission standards Type of Specified Scale of facilities Facilities (Capacity of incineration) Waste incinerators More than 4t/h (hearth area is 2t/h – 4t/h more than 0.5 m2 Below 2t/h or capacity of incineration is more than 50 kg/h) Electric steel-making furnaces Sintering facilities for steel industry Facilities for collecting zinc Facilities for manufacturing aluminum base alloy (Unit: ng-TEQ/m3 N) Standards for Standards new facility for existing facility 0.1 1 28 1 5 5 10 0.5 0.1 1 1 5 1 10 5 2) Effluent standards (Unit: pg-TEQ/L) Type of Specified Facilities Standard • Bleaching facilities using chlorine or chlorine compounds used for manufacturing sulfate pulps (kraft pulps) or sulfite pulps. • Cleansing facilities for acetylen used for manufacturing acetylene by carbide method • Cleansing facilities for waste gas used for manufacturing potassium sulfate • Cleansing facilities for waste gas used for manufacturing alumina fiber • Cleansing facilities for dichloroethane used for manufacturing vinyl chloride monomer • Sulfuric acid concentration facilities, cyclohexane separation facilities, and waste gas cleansing facilities used for manufacturing caprolactam (limited to using nitrosyl chloride) • Water washing facilities and waste gas cleansing facilities used for manufacturing chlorobenzene or dichlorobenzene • Filtering facilities, drying facilities and waste gas cleaning facilities used for manufacturing of sodium hydrogen 4-chlorophthalate • Filtering facilities, drying facilities and waste gas cleaning facilities used for manufacturing of 2,3-dichloro-1,4-naphthoquinone • Nitro-derivative and its reductant separation facilities, nitro-derivative and 10 its reductant cleansing facilities, dioxazineviolet cleansing facilities, and hot-air drying facilities used for manufacturing dioxazineviolet • Cleansing facilities for waste gas and wet dust collecting facilities relating to roasting furnaces, melting furnaces or dry kilns used for manufacturing aluminum or aluminum–base alloy • Refining facilities, waste gas cleansing facilities, and wet dust collecting facilities used for recovering of zinc ( limited to zinc recovery from dust that is generated from electric steel-making furnaces and collected by dust-collector) • Cleansing facilities, wet dust collecting facilities, and ash storing facilities which are related to waste incinerators (hearth area is more than 0.5m2 or capacity of incineration is more than 50kg/h) and discharge sewage or waste solution • Resolving facilities for waste PCB or PCB-processed products • Cleansing facilities for PCB contaminated matter or PCB-processed products • Facilities for disposing water discharged from plants or business places with facilities mentioned above • Terminal treatment facilities for sewerage relating to facilities mentioned above Note 1: The standard relating to water discharged from terminal waste disposal facilities is 10pg-TEQ/L based on instructions stipulating standards for maintenance and management based on the Wastes Disposal and Public Cleaning Law. 29 COMMENTS SUBMITTED BY JORDAN 30 COMMENTS SUBMITTED BY MEXICO 31 32 COMMENTS SUBMITTED BY PERU Consideraciones Generales Consideramos muy importante la elaboración y difusión de estas guías técnicas ya que nos permitirán promover la aplicación de las Mejores Técnicas Disponibles (BAT) y las Mejores Prácticas Medioambientales (BEP) sobre Contaminantes Orgánicos Persistentes (COPs) en nuestro país. En el Perú se viene realizando el Proyecto: “Inventario de Existencias de PCBs e Identificación y Cuantificación de Liberación de Dioxinas y Furanos” y se está por dar inicio al proyecto “Plan Nacional de Implementación de para la Aplicación de COPs en el Perú” por lo que estas guías serán de mucha importancia. Sobre los temas que se están por desarrollar en las guías Consideramos necesario recomendaciones en los relacionado a la forma correcta de usar estas guías y a la forma adecuada de aplicarlo, por este motivo pedimos que se tomen en cuenta estas consideraciones durante el desarrollo de la parte C del Capítulo I: “Como usar estas guías”. Tomando en cuenta que en nuestro país todavía no se aplica una normatividad específica en lo referente a la aplicación de Convenios Internacionales como el de Estocolmo, creemos importante que se termine de desarrollar el punto E del Capítulo III en lo referente a aspectos legales para la aplicación de estas guías. Teniendo el Perú una Ley de Cementerios y Servicios Funerarios y siendo la cremación de cadáveres una práctica que se da en nuestra patria, en muchos casos sin tomar en cuenta la liberación de los COPs, creemos muy oportuno y satisfactorio que se desarrolle el punto F del Capítulo VI sobre Cremación, ya que permitirá la aplicación de las BAT y BEP en esta actividad. Sobre temas que proponemos se incluyan Sugerimos que se considere el desarrollo de la Aplicación de BAT y BEP en el Desguace y Desmantelamiento de Navíos y Embarcaciones. Creemos que esta actividad, cuando se lleva a cabo en malas condiciones, no permite una buena separación de COPs como los aceites y PCBs y una mala disposición de las fracciones ligeras (restos de pinturas, aceites, plásticos y otros) libera Dioxinas y Furanos cuando la incineración de estos se realiza en condiciones no controladas. En nuestro país se viene realizando esta actividad y creemos que con la aplicación de las BAT y BEP se controlará la liberación de estos COPs. Sobre los Temas Desarrollados d.1) Incineradores de Desechos Municipales y Peligrosos Si bien es cierto que en las técnicas de combustión del capítulo 6 sobre BAT nos indican los parámetros a controlar para asegurar una buena combustión, creemos necesario que se mencionen las características de las cenizas resultantes de la incineración que se deben analizar y determinar para verificar que se ha realizado una buena combustión. Creemos conveniente que en el capítulo 3 sobre Diseño y Operación de Incineradores de la sección V.A.I correspondiente a la Incineración de Desechos, se incluya diagramas de flujo y su respectiva descripción del proceso de incineración especificando la ruta que sigue el desecho para los diferentes tipos de procesos de incineración. 33 d.2) Incineración de Desechos Hospitalarios En cuanto a la inclusión de BAT y BEP en la incineración de desechos peligrosos y hospitalarios, así como el autoclavado, lo consideramos importante y oportuno ya que en nuestro país se está empezando a utilizar estas técnicas y la aplicación adecuada de estas guías nos permitirá realizarlas sin perjuicio de la salud y el medio ambiente en lo referente a los COPs. En el Perú todavía no aplicamos la incineración de desechos municipales. d.3) Hornos de Cemento De la misma forma la incineración de desechos peligrosos en hornos de cemento en el Perú todavía no es una práctica autorizada y siendo un problema la disposición de residuos peligrosos que contienen COPs como residuos de aceite y envases de plaguicidas, consideramos oportuno y adecuado que se haya desarrollado el capítulo referente a las BAT y BEP en la incineración de residuos peligrosos en hornos de cemento lo que nos permitirá tener una alternativa limpia sin liberación de COPs en la disposición de residuos peligrosos como los plaguicidas. d.4) Idioma y Vocabulario Siendo necesario la difusión de estas guías entre todos los sectores involucrados en nuestro país como el sector industrial en el marco de la Implementación del Convenio de Estocolmo, consideramos adecuado se publiquen estas guías en el idioma español y se establezca un glosario de términos generales utilizados en estas guías. Consideraciones Finales Estando nuestro país en un proceso de desarrollo y considerando que el objetivo del Convenio de Estocolmo es proteger a la salud humana y el medio ambiente frente a los contaminantes orgánicos persistentes, creemos que la aplicación de estas guías en nuestro país serán una gran herramienta para lograr el objetivo. _______________________ Ing. Domitila Briones Yañez DIGESA – Ministerio de Salud PERU 34 COMMENTS SUBMITTED BY THE PHILIPPINES SUBJECT: Comments on the Draft Guidelines on Best Available Techniques and Best Environmental Practices The Philippines currently has two (2) projects associated with POPs: o Philippine Enabling Activity Project – Initial Assistance to the Philippines to Meet Its Obligations Under the Stockholm Convention on Persistent Organic Pollutants (POPs) o Demonstration of Viability and Removal of Barriers that Impede Adoption and Effective Implementation of Available, Non-Combustion Technologies The Draft Guidelines on Best Available Techniques and Best Environmental Practices provides very useful information especially in choosing the most economical yet environmentally-sound technologies and processes in areas where there is a possibility of POPs release into the environment. The guidelines and suggestions are very useful in formulating regulations and policies to further reduce and manage POPs. In the issue of incineration, Republic Act 8749, or the Clean Air Act of the Philippines, banned the use of incineration which is a major contributor to the release of dioxins and furans. We are now in the process of formulating our National Implementation Plan (NIP) which is the final output of the Philippine Enabling Activity Project on POPs. The other activities conducted under this project were the Initial National Inventory on POPs, Capacity and Needs Assessment for the Country’s Compliance to the Stockholm Convention, and the Public Awareness and Information Campaign Program. The Draft Guidelines on BAT and BEP will be used as a basis in prioritizing goals and policies for the country’s compliance to the Stockholm Convention through the NIP. The guidelines listed are comprehensive and covers most of the processes being used in our country. But due to economic constraints, crude equipment and processes are being employed by the industry to perform these processes which lead to release of POPs. Future policies and guidelines on the management of POPs releases will be based from these guidelines and these will be reflected on the priorities and objectives that will be set for the National Implementation Plan (NIP). ANGELITA T. BRABANTE POPs Project Coordinator 35 COMMENTS SUBMITTED BY SLOVAKIA Ministry of the Environment of the Slovak Republic Waste management department Bratislava Number: 14.6.2004 682/2004-min 241/2004-6 809/2004-6.2 [email protected] Slovak comments on draft guidelines on BAT and guidance on BEP relevant to Article 5 and Annex C of the Stockholm Convention on POPs Slovakia welcomes these both document prepared by the Expert Group for next session which be held in October 2004 in Japan. We agree with discussed versions. Concerning the draft guidelines on best available techniques, Slovakia is of the opinion that it is a very important issue also as a basis for the giving a right statement on establishing several new waste recovery and waste disposal installation at regional and district level. It is also needed to ensure the application of the most appropriate combination of environmental control measures and strategies in the practice. To ensure it by the way ”guidance on best environmental practices” seems to be a very good idea in view of the need to ensure control not only waste handling but also the conditions of production processes and of the marketing. We hope that in the future we will be able to find some our experts to joint in discussion by E-mail on several documents from this area thanks to implementation of the Regulation of the European Parliament and of the Council on POPs amending Council Directive 79/117. It seems to be good basis for mutual work government-designated experts in the field of the best available techniques and best environmental practices. In Slovakia there are on going following international projects to help us to be prepared to implement the Stockholm Convention on POPs: 1. “Initial assistance to the SR to meet its obligations under the Stockholm Convention on POPs” 2. “Demonstration of Viability and Removal of Barriers that Impede Adoption and Effective Implementation of Available, Non-combustion Technologies” 3. ”Dioxin emissions in Candidate Countries” 4. Strengthening of Institutional Basis for Safe management of Chemicals” 5. ”Regional approach for the environmentally sound management of POPs as waste in selected CEE countries”. We hope that thanks all these projects Slovakia will be able to find national experts for next mutual work in the field of the best available techniques and best environmental practices and to ensure efficient functioning co-operation in the future. Prepared by: Ing. Marta Fratricova from the Waste Management Department at the Ministry of the Environment of the Slovak Republic (WMD of the MoE of the SR). Approved by: Ing. Peter Gallovic, Head of the WMD at the MoE of the SR Ing.Ivan Mojík, Designated Head of the Environment Protection Section at the MoE of the SR 36 COMMENTS SUBMITTED BY TRINIDAD AND TOBAGO 37 38 COMMENTS SUBMITTED BY THE UNITED STATES OF AMERICA United States Comments on International BAT/BEP Guidelines for Unintentional POP’s Processing of Metals (Papers under sections V.D. & VI. B.) 1) The results presented in the paper for dioxins/furans (D/F) from secondary aluminum production, magnesium production, and sinter plants in the iron and steel industry are consistent with what we know about US plants. 2) For primary aluminum production, the paper presents that D/F were judged not to be significant, and that is consistent with what we found in the US. 3) We have no data for D/F from US electric arc furnaces (EAFs), so we do not know how applicable the results in the paper are. However, the techniques discussed for reducing D/F from EAFs are consistent with some of those we are considering in the US (the US regulation related to EAF’s may get co-control of D/F). Primary measures mentioned in the EAF paper for D/F control are: i) Reducing contaminants such as oil, plastics, and other hydrocarbons in the scrap (which also reduces VOC and volatile HAP) ii) Proper operation of the EAF (reducing air infiltration, replacing the roof cover after charging, avoiding operational delays) iii) Adequately sized evacuation system iv) Continuous parameter monitoring system (to make sure everything is operating properly) Secondary measures include: i) Having an efficient dust collecting system such as a baghouse, because higher dust collection relates to better D/F control. Also mentioned are other control methods using post combustion/rapid water quench and carbon injection, neither of which are used at US plants (some European plants have these). It is indicated that there might be some site-specific considerations (space, configuration, cost) that might limit the applicability of these techniques to existing plants. 4) Overall, secondary steel recommendations for control seem reasonable. Production of pulp using elemental chlorine or chemicals generating elemental chlorine for bleaching (Section V.C.) No comments on these guidelines, other than some grammatical and typographical errors. Open burning of wastes (Section VI. A.) This Annex is well written and clearly understood. For the most part it appears to be technically correct. Comments by section: Section 1 1) We would not qualify those devices that are merely drums as “incinerator.” BAT incineration also includes provisions for removal of particulate matter and acid gases, not just provisions to minimize dioxins. 2) I would not make a comment on the use of open piles as a method of reducing dioxins. The Lemieux et al (2003) study only had 1 data point for open piles and the dioxin emissions data for that 1 test were within the spread of the baseline combustion condition. There are not sufficient data to support assumptions that open pile combustion will have higher (or lower) dioxin emissions. 3) Is there really evidence that fireworks are a substantive source? 4) In the last sentence of Section 1, I think you mean upwind of residential areas not downwind. 39 Section 2 1) The first sentence is not a sentence and perhaps should begin with: “In general, this includes…” 2) “geographical boundaries to be burned” is awkward. Instead, it could read “Intentional burning may not constitute well-controlled combustion, even if the area to be burned is well defined.” (Section 2.1.1) 3) Do inhibitors “adversely effect” dioxin formation? (Section 2.1.1) 4) I have not seen any studies that suggest that application of herbicides or pesticides produced increased risk of PCDD/F formation. (Section 2.1.5) 5) Note that it is not clear that small prescribed burns lead to less PCDD/F than “more devastating inadvertent burns.” (Section 2.1.5) Section 3 1) This section notes that there has been significant study of open burning of wastes. This is not an accurate characterization. Further, the reference provided, #7, deals with forest fires, not waste. (Section 3.1.1) 2) The statement: “Variation in waste among countries” is probably true. However, a reference would help. (Section 3.1.1) 3) “Garbage” and “refuse” are not synonymous. Garbage is putrescible organics; refuse is all of the other stuff. Those are definitions from the field of environmental engineering. (Section 3.1.1) 4) “Burnings should be a last resort…”. The word “open” should be inserted at the beginning of this sentence, otherwise this statement (and perhaps others like it earlier in the document) is not supported by evidence presented in this document. It should not be presented a priori without this sufficient caveate. For example, composting is given the impression as a more favorable option. But what if the compost is used for subsistence farming, resulting in substantial heavy metal ingestion? What if the recycling processes (e.g., waste aluminum) result in substantially more PCDD/F than a modern waste to energy facility? (Section 3.2.5) Section 4 1) Tires do not necessarily have a relatively high amount of sulfur. It would be more accurate to say that tires have a similar amount of sulfur as is found in medium sulfur coals. Open burning of tires produces huge amounts of particulate matter (mostly a carbon black type of particulate) as well as PAHs (particularly Benzo(a)pyrene and benzene). In addition open burning of tires produced an oozing oily liquid that can contaminate ground water. 2) Tires have also been successfully used in rubber modified asphalt which greatly extends the lifetime of the pavement (Section 4.2.4). References Lemieux, P.M.; Gullett, B.K.; Lutes, C.C.; Winterrowd, C.K.; Winters, D.L. (2003), "Variables Affecting Emissions of PCDDs/Fs from Uncontrolled Combustion of Household Waste in Barrels," AWMA J, Vol. 53, pp. 523-531. 40 COMMENTS SUBMITTED BY MEMBERS OF THE EXPERT GROUP COMMENTS SUBMITTED BY PROF. ALAMIR BARKAHOUM (ALGERIA) 1-INCINÉRATION DE BIOMASSE NON ASSOCIÉE À L’ÉNERGIE 1-a Nettoyage pour l’agriculture - Pratiques d’incinération du chaume de blé interdite - Le reste des déchets est enfouis lors des labours - Certains déchets sont transformés en aliments de bétail A) Composition des déchets - Mauvaises herbes - Reste des moissons - Broussailles diverses B) Barrières à l’effet d’éliminer l’incinération à ciel ouvert Remède Barrière Ignorance Education et sensibilisation Manque d’informations Création de cellule d’information au niveau des communes. Manque de Moyens L’état doit aider l’agriculteur par un financement ou des prêts. C) Documents Politiques Spécifiques - Loi n°93-03 du 05/02/83 relative à la protection de l’environnement. - Loi n° 01-19 du 12/12/01 relative à la gestion du contrôle et à l’élimination de déchets. - Loi n° 01-20 du 12/12/01 relative à l’aménagement du territoire et du développement durable. D) Minimisation des Déchets/ Stratégies de Diversion Traitement des sols par des désherbants. E) Alternatives disponibles concernant l’incinération à ciel ouvert Dégradation naturelle pour éviter l’incinération. F) Techniques d’incinération et attributs Les déchets sont brûlés à l’air libre, sans aucun contrôle. G) Techniques d’amélioration Propositions d’incinération contrôlés par combustion bien aérée H) Variation Régionale Trois principales catégories de régions : - Partie nord : oléagineux, primeurs - Haut plateau : céréales - Partie sud : primeurs et palmiers I) Commentaires Les déchets générés par « Nettoyage pour l’Agriculture » ne posent pas véritablement un problème de pollution en Algérie, néanmoins, un contrôle de leur gestion doit être mis en place à l’avenir. I-b Feux de forêts imprévisibles • A) Types de matériaux d’alimentation/composition En Algérie les espèces les plus dominantes sont : - le pin d’Alep : localisé généralement en montagne (Atlas Blidéen, kabylie) 41 - le liège : localisé le long de la côte Est Algérien (jijel, collo). • Il n y a pas de résidus de bois de forêts du fait de l’inexistence d’industrie forestière. • Les grandes surfaces forestières sont gérées par le ministère de l’Agriculture (Direction Générale des Forêts). Les feux de forêts imprévisibles se déclarent généralement durant la période estivale. Ils généralement sont provoqués. • Les types de forêts varient avec la géographie (ex : espèces, densité, taille, etc.) [Non dépendant de l’état de développement du pays] ; Résidus de bois laissé dans les forêts par rapport à tous les arbres/buissons ; • • La biomasse par hectare dépend des espèces, de la géographie, du climat ; • Les différentes espèces peuvent avoir différentes concentrations de produits chimiques dangereux, ex : le contenu du chlore ; • Les forêts peuvent être gérées ou naturelles ; • Les forêts peuvent être traitées avec des produits chimiques, qui constituent soit, des précurseurs des PCDD /PCDF (ex : 2,4,5 d’acide trichlorophénoxyacétique (2,4,5-T) 2,4d’acide dichlorophénoxyacétique (2,4-D) du pentachlorophénol dans le cas des résidus de bois) soit des métaux catalytiques, (ex : du cuivre) soit des inhibiteurs, (ex : du sulfure) ; • Les feux de forêts peuvent être accidentels ou le fait d’incidences. B) Barrières pour éliminer les Feux de Forêts Barrière 1. Départ naturel : température Remède la - Nettoyage et élimination de corps pouvant déclencher un feu. - Aménagement d’accès et d’installation de coupes feux. 2. Imprudence, Ignorance des dangers - Education - Réglementation stricte - Renforcement de moyens de gardiennage. 3. Feux intentionnels pour récupération - Renforcement de gardiennage du bois - Renforcement et application de la législation. 4. Terrains difficiles - Prévoir l’équipement adéquat. élévation de C) Documents Politiques Spécifiques • Application de la législation en vigueur relative à la protection des forêts (décret de 1987). D) Minimisation des occurrences, Taille/Impact • Il existe un plan de renouvellement des forêts qui se traduit annuellement par des campagnes de reboisement (exemple du Barrage vert pour lutter contre la remontée du désert). • Aucune réglementation disponible n’autorise l’incinération à ciel ouvert. • Renouvellement de la forêt • Interdiction de permis pour des brûlages prescrits • Interdiction générale • Réduction des permis (ex : seulement dans les régions éloignées ayant une faible exposition aux humains/ production de l’alimentation) ; 42 • • • • • • Réduction à de la végétation à brûlage rapide Restreint aux régions qui fournissent de bonnes conditions de combustion Dés que cela arrive, il faut protéger les humains, les animaux, et les marchandises de l’impact direct du feu (y compris les avertissements, et peut-être l’évacuation) ; Au déclenchement du feu , s’assurer qu’il y en place un système à activer pour l’éteindre. Au déclenchement de l’incendie, des mesures de prévention/ de minimisation de l’étalement des résidus brûlés doivent être initiées (ex : la gestion des cendres si nécessaire) ; Initiez des contre-mesures pour limiter l’impact. E) Alternatives disponibles concernant l’Incinération à Ciel Ouvert • Nettoyage manuel irrégulier • Les gardes forestiers sont équipés de moyens de communications, en plus d’installation de miradors pour les grands espaces. La protection civile intervient rapidement à l’aide de moyens mis à sa disponibilité. • L’infrastructure d’intervention rapide existe depuis longtemps, mais reste cependant insuffisante quand il s’agit de terrains accidentés. • Nettoyage mécanique (pour les brûlures dues à des incendies) • Les impacts des accidents peuvent être limités seulement par l’intervention rapide pour éteindre le feu • Pour empêcher la gravité : interdiction de l’utilisation / application de précurseurs ou de métaux catalytiques de formation de PCDD/PCDF ; F) Les Incinérations- peuvent varier d’une région à une autre • Les causes d’incendies sont à la fois intentionnelles et accidentelles. • Les feux de forêts se déclenchent pendant la période des grandes chaleurs (forêts sèches, incendies avec flammes). • Dans les zones accessibles, les feux de forêts sont généralement circonscrits rapidement, contrairement aux zones accidentées où les feux ravagent totalement la zone boisée. Les cendres générées se déplacent parfois jusqu’aux zones habitées. • Causes : Intentionnelle « » Accidentelle • Feu chaud à ciel ouvert dans les forêts sèches • Le brûlage lent sans flamme dans un environnement humide (note : l’humidité ne peut pas augmenter indéfiniment) • La longueur de temps du feu et donc, le nombre d’arbres/ buissons brûlés G) Techniques d’amélioration abattements Il n’existe pas d’incinération de déchets de forêt à ciel ouvert programmées. Ce type de déchets se dégradent naturellement. H) Variations régionales I) Commentaires Les feux de forêts accidentels, ne peuvent pas être évités, et se produisent surtout en été (Juillet-Août). Divers mesures sont prises par les pouvoirs publics, pour minimiser le déclenchement des feux de forêts (nettoyage des espaces, surveillance renforcée, et existence d’un plan ORSEC pendant la période estivale). I-c Nettoyage de la végétation pour préparer la moisson • A) Composition des déchets. Matériau organique dérivé des plantes. Une source de plantes spécifique peut varier, et peut avoir un petit effet. 43 B) Barrières pour éliminer les incinérations à ciel ouvert Barrière 1- Ignorance, manque d’informations 2 - Moyen A) B) C) • • Remède Education et sensibilisation L’état doit aider l’agriculteur par un financement sous forme de prêt Documents Politiques Spécifiques Minimisation des déchets Alternatives disponibles à l’incinération à ciel ouvert Retrait mécanique avec addition de nutriments Les techniques de plantation sans incinération (pour des cultures appropriées) D) Techniques d’incinération et Attributs E) Techniques d’Amélioration • Choix des jours pour permettre la réduction de l’exposition des humains à la fumée F) Commentaires 2- FEUX DE DÉCHARGES PUBLIQUES (Intentionnels ou imprévisibles) A) Composition des déchets Les déchets solides mis en décharge, subissent une récupération à hauteur de 20 %. Les produits récupérés pour un éventuel recyclage sont :les matières plastiques et certains matériaux. Cette récupération est faite par des « chiffonniers » qui leur permet un gain substantiel. Ces décharges publiques ne sont pas totalement gérées ce qui entraîne pour la majorité d’entre elles des combustions non contrôlées. B) Barrières pour éliminer les incinérations à ciel ouvert Barrière 1.Recherche de terrains adéquats (sol imperméable loin des habitations, voies d’accès rapides etc. …) 2. Accès non contrôlé 3. Canalisation des Bio gaz formés 4.Tri en amont (à partir de la ménagère) 5. Ramassage Remède *Etude d’impact pour l’implantation des décharges contrôlées *Gestion rigoureuse des CET *Mise en place de centres d’ enfouissement techniques à travers le territoire national. *Meilleures pratiques de gestion (clôture, gardiennage, contrôle des déchets, etc. …) *Dans les CET au stade de la réalisation, des bio gaz formés sont collectés et brûlés (torchères) *Utilisation des bio gaz comme source d’énergie. *Sensibilisation *Mettre à la disposition des ménagères des sachets de couleur différente pour le tri. *Rentabiliser et renforcer les moyens de collectes *Ramassage des déchets à des horaires convenables. C) Documents politiques • Des textes réglementaires concernant la gestion des déchets solides existent : - Loi n°93-03 du 05/02/83 relative à la protection de l’environnement. - Loi n° 01-19 du 12/12/01 relative à la gestion du contrôle et à l’élimination de déchets. 44 - Loi n° 01-20 du 12/12/01 relative à l’aménagement du territoire et du développement durable. • Avec l’ouverture prochaine des centres d’enfouissement technique (CET) l’incinération à ciel ouvert bne posera plus de problème ; les bio gaz sont brûlés à travers les torchères. D) Minimisation des Déchets / Stratégies de Diversion • La stratégie algérienne en matière de gestion des déchets solides, se base essentiellement sur les points suivants : Le tri en amont qui permettra de recycler certains déchets et produire un composant pour les besoins de l’agriculture. E) Alternatives disponibles à l’incinération à ciel ouvert de ces déchets Les centres d’enfouissement techniques représentent une alternative à l’incinération des déchets à ciel ouvert.. Dans ce cadre, l’Algérie, a lancé un programme de réalisation de 48 CET. Ces CET régleront le problème d’utilisation de grandes surfaces et les émanations de fumées. F) Techniques d’incinération et attributs Dans les zones rurales, les habitants incinèrent eux mêmes leurs déchets. G) Techniques d’amélioration A travers le tri qui se fera en amont, il est possible d’améliorer l’incinération en évitant les combustions génératrices de dioxines et furannes. H) Variations Régionales/Commentaires Dans les grandes agglomérations les déchets générés sont plus diversifiés et susceptibles d’émettre des dioxines et furannes et leur gestion doit être prise en charge d’une manière différente que la gestion des déchets provenant des zones rurales. 3- DÉCHETS RÉSIDENTIELS A) Composition des Déchets L’organisme chargé de la gestion des déchets au niveau d’Alger (NETCOM) envisage une étude sur la composition des déchets produits par la population de la ville. La quantité de ces déchets a été estimée en 2003 à un million de tonne, constitués principalement de déchets ménagers (humides). B) Barrières pour éliminer l’incinération à ciel ouvert Barrière Remède .1. Recherches de terrains adéquats *Etude d’impact pour l’implantation des (sol imperméable loin des habitations, décharges contrôlées voies d’accès rapides etc …) *Gestion rigoureuse des CET *Mise en place de centres d’enfouissement techniques à travers le territoire national. 2.Accès non contrôlé Meilleures pratiques de gestion (clôture, gardiennage, contrôle des déchets, etc 3.Canalisation des Bio gaz formés Dans les CET au stade de la réalisation, des bio gaz formés sont collectés et brûlés (torchères) *Utilisation des bio gaz comme source d’énergie. 4.Tri en amont (à partir de la ménagère *Sensibilisation *Mettre à la disposition des ménagères des sachets de couleur différentes pour le tri. 5. Ramassage *Rentabiliser et renforcer les moyens de 45 collectes *Ramassage des déchets à des horaires convenables. 4) DÉCHETS COMMERCIAUX • • A) Composition des déchets Aucune étude n’a été faite concernant ce type de déchets. D’une manière générale, les déchets commerciaux sont considérés comme les déchets municipaux et sont donc collectés et mis en décharge comme des déchets ménagers. B) Barrières à l’élimination d’incinération à ciel ouvert Barrière Remède 1. Aucune distinction *Réglementation juridiquement contraignante. *Sensibilisation. 2. Pas de tri *Faciliter et encourager les tris * Mettre les moyens à la disposition des concernés pour faciliter le tri. 3. Décharges spécifiques à ce type *Ouvrir des décharges adéquates. de déchets 4. Quantité insuffisante pour *Prévoir des collectes périodiques. justifier la collecte 5. Moyens de collecte non *Mettre les moyens adéquats de collecte de ces spécifiques. déchets. C) Documents politiques Spécifiques • Interdire la mise en décharge de ce type de déchets avec les déchets ménagers. • Selon le principe pollueur –payeur, une taxe sur les déchets est instaurée en Algérie. • L’Algérie est dotée d’une réglementation concernant la gestion de déchets solides. • Un programme interministériel, sur la gestion des déchets solides, et donc des déchets commerciaux, a été initié et mis en application. D) Minimisation des déchets/ Stratégies de Diversion Les emballages utilisés en Algérie proviennent en majeure partie de l’importation. Actuellement, il n’existe pas de structures qui utilisent des techniques de réduction de ces déchets. Certains emballages sont récupérés par le recyclage (cartons, plastiques, emballage métallique). E) Alternatives disponibles à l’incinération à ciel ouvert Comme déjà proposé plus haut, prévoir des cycles de collectes périodiques, et l’ouverture de décharges publiques appropriées à ce type de déchets. Un tri, avec possibilité de recyclage sur site peut être envisagé pour la réduction des déchets. F) Pratiques d’incinération : Dans ce domaine, l’Algérie n’a pas d’expérience car aucune pratique d’incinération n’a été mise en œuvre. G) Techniques d’Amélioration Il n’existe pas d’incinération de déchets de forêt à ciel ouvert programmées. Ce type de déchets se dégradent naturellement A) Commentaires Les déchets sont généralement volumineux, donc il est plus facile de procédé a un tri. Prévoir des unités de récupération permettant de réduire ces déchets. 46 Ce type de déchets nécessite une gestion demandant des moyens spécifiques. 5-DÉCHETS DE CONSTRUCTION ET DE DÉMOLITION A) Composition des Déchets Les déchets de construction et de démolition se composent principalement de béton, d’acier, de brique et à un degrés moindre de verre et de bois. Des sites appropriés existent à travers le territoire Algérien. Ces déchets sont concassés et utilisés dans le revêtement des routes. B) Barrières à l’élimination d’incinération à ciel ouvert Barrière 1. Manque de moyens de recyclage 2. Manque de décharges appropriées 3. Pas de tri avant la mise en décharge 4. Technique de demolition 5. Recyclage Remède *Encourager l’ouverture de centres de recyclage *Aménager des espaces appropriés pour recevoir ces déchets *Encourager les entrepreneurs à réaliser un tri en amont. *Utilisation des techniques modernes de démolition (explosifs, etc …) *Valoriser les produits recyclés (Gravats pour revêtement, acier, bois) C) Documents spécifiques • • Inciter les investisseurs dans le recyclage de ces déchets, en valorisant les différents produits. Prendre des dispositions réglementaires pour le contrôle et le processus de démolition et de mise en décharge. D) Minimisation des déchets/ Stratégies de Diversion • Lors des démolitions de constructions, une séparation des divers composants (béton, briques, acier, bois, verre, etc…) se fait généralement sur site. Les produits récupérés sont réutilisés. E) Alternatives disponibles à l’incinération à ciel ouvert En Algérie, cette catégorie de déchets ne subit pas d’incinération à ciel ouvert. F) Techniques d’incinération- peuvent varier d’une région à une autre • Aucune incinération G) Techniques d’Amélioration • Aucune incinération H) Variations régionales I) Commentaires • Une grande partie des déchets de démolition, en raison de leur valeur ajoutée ; est réutilisée, dans divers secteurs notamment dans les travaux publics et matériaux de construction. • Il existe des sites spécialement aménagés pour recevoir ces déchets. 47 6- EQUIPEMENTS MILITAIRES/MUNITIONS 7- INCINÉRATION À CIEL OUVERT DES DÉBRIS POST CATASTROPHIQUES A) Composition des déchets • • • Déchets de démolition d’habitations (dans le cas d’un séisme). Déchets provenant d’inondations (boues, détrituces de toutes sortes). Explosions accidentelles d’usines (hydrocarbures, produits chimiques et le bâti). B) Barrières pour l’élimination de l’incinération à ciel ouvert Barrière 1 Réglementation vigilance Remède de *Prévoir une réglementation stricte et contraignante permettant une vigilance plus accrue. 2. Pas de contrôle et de suivi *Mettre en place un comité intersectoriel pour le contrôle et le suivi. *Mettre en place un comité de contrôle et de suivi, au niveau des installations à haut risque pour une bonne application des textes en vigueur. 3. Manque de communication *Equipements de brigades d’intervention en matériel adéquat. 4. Manque de moyens d’intervention *Education hygiène et sécurité et rapide information sur les risques, vulgarisation des conduites à tenir en cas de catastrophe. 5. Manque de plan de prévention et *Chaque secteur doit avoir un plan exercices de stimulation. d’intervention rapide. *Prévoir des exercices de stimulation annuellement. 6. Formation de personnel *Former des spécialistes à cet effet (Protection civile, santé, forces armées). .et manque C) Documents politiques spécifiques • Application de la législation en vigueur relative à la protection des forêts (décret de 1987). D) Minimisation des déchets/stratégie de diversion • Prévention : agir en amont • • • Respect des normes de sécurité (construction et matériaux) Prévoir des brigades d’intervention rapide Gestion rationnelle des déchets après une catastrophe. E) Alternatives disponibles à l’incinération à ciel ouvert • Récupération et recyclage le plus large possible. F) Techniques d’incinération et attributs G) Techniques d’Amélioration F/G/H Techniques d’incinération/d’amélioration/ commentaire 48 • Dans le cas de l’Algérie, les déchets provenant des catastrophes, sont pour certains recyclés et récupérés et pour le reste mis en décharge. 8- FEUX ACCIDENTELS A) Composition des déchets Bois, papier textiles, plastiques, essence, vernis, asphalte. Le pourcentage dépend du type d’objets en feu ( Ex : maisons, commerce, agricoles, constructions publiques et voitures et autres véhicules B) Barrière à l’élimination d’incinération à ciel ouvert Barrière 1. Manipulation imprudente de feux 2. Equipements électriques défectueux et installations électriques vétustes. 3. Accidents de la circulation. 4. Accidents dans l’industrie 5. Activités criminelles Remède *Education et information sur les risques. *Norme de sécurité des produits *Contrôle périodique des installations. *Mesures de prévention et campagnes de sensibilisation. *Respect des normes de sécurité *Contrôle périodique des équipements. *Surveillance et gardiennage *Vigilance et mesures de sécurité. C) Documents politiques spécifiques • Loi sur les risques majeurs et les grandes catastrophes ( juillet 2003). D) Minimisation des déchets • Intervention efficace et rapide des équipes d’intervention E) Alternatives disponibles Aucune F) Techniques d’incinération Pas d’incinération G) Techniques d’amélioration • Former et sensibiliser et éveiller les consciences • Améliorer les mesures d’intervention • Renforcer les contrôles de sécurité. H) Commentaires • Dans le cas de l’Algérie, après un feu accidentel, les déchets générés sont mis en décharge et ne subisse aucune incineration. 49 COMMENTS SUBMITTED BY MR. PATRICK FINLAY (CANADA) -----Original Message----From: Ternan,Sarah [NCR] [mailto:[email protected]] Posted At: 16 June 2004 22:47 Posted To: SSC Conversation: Canada Comments RE: Draft Guidelines and Guidance on BAT and BEP Subject: Canada Comments RE: Draft Guidelines and Guidance on BAT and BEP Importance: High On behalf of Patrick Finlay, Canada's member of the Stockholm Convention Expert Group on Best Available Techniques (BAT) and Best Environmental Practices (BEP), please find below comments and information for various source sector draft BAT/BEP documents for consideration. Regards, Sarah Ternan for Patrick Finlay Environment Canada ----------------------------------------------------------Section V.A.1 - Waste Incinerators: Medical, Hazardous and Sewadge Sludge Under Section 3.3.1.2 there should be a distinction made between chlorinated and non-chlorinated wastes when discussing temperatures. Temperatures of 850-1000 C can be considered adequate for destruction of non-chlorinated hazardous waste; while 1000-1200 C is considered adequate for destruction of chlorinated hazardous waste, i.e. dioxins and furans, PCBs and HCB. This issue is raised as these guidelines identify "pass through" as one source of unintentional POP release. Also - for consideration by the authors/country leads for both the document noted above and section V.A.2 (Medical Waste incinerators) - Canadian emission limits for the above designated sources can be found in the attached files (Canada-wide Standards for Dioxins and Furans, May, 2001 and accompanying stack test requirements). http://www.ccme.ca/initiatives/standards.html?category_id=50#23 <<d_f_incin_stk_tst_rqmts_e.pdf>> <<d_and_f_standard_e.pdf>> Section VI.C Residential Combustion Sources Additional clarification would be beneficial for Tables 1 & 3. A reference or notation of the source of the emission factors should be included for these tables. In Table 3 - it's suggested that further explanation be included to better clarify the differences in the two sets of PCDD/PCDF release estimates. For the section on recommendations, it is suggested that an annex of information sources relating to 'improved wood stoves' be compiled and included, as may be possible. Such a list of information sources could be useful for all countries (developed, developing and those with economies in transition) in developing their National Implementation Plans and associated Action Plans. Section VI.E Firing installations for wood and biomass Suggest that the recommendation in Table 3 regarding the primary measure "Increased residence time of flue gases upstream of the boiler" be further expanded and/or clarified. Section V.C Production of Pulp It's recommended that sections 1.3 and 2.2.1 be included in the BAT/BEP document for this source (in response to the question posed by the country lead/author). Additional information and details could be appended or included, as deemed appropriate to assist countries in the effective minimization/elimination of UPOPs from pulp production generally. 50 COMMENTS SUBMITTED BY PROF. MARAT ISHANKULOV (KAZAKHSTAN) Dear colleagues, My comments on the proposed variant of “Best Available Techniques – Best Environmental Practices (BAT-BEP) for Open Burning of Waste” text are as follows. 1. I think it advisable in Section 1,0 (General Guidance) to make a special note of whom the Guidance is addressed. In my opinion, it is most urgently needed by developing countries and countries with economies in transition. In these countries all forms of open burning are widely spread, frequently without any scientifically-based background. Besides, the use of best techniques and best environmental practices in this field is a key to solving social problems of local communities and promoting their democratization. For this reason I highly appreciate this very section - «open burning» of the Guidance on BAT & BEP. 2. The classification of open burning types is not perfect yet in spite of all efforts to improve it. Though this part of the Guidance BAT and ВЕР considers only open burning of waste, item 4.3 addresses not only waste. Such categories as «crude oil» and «oil well» do not fall into waste. Military Ordinance/Munitions (item 4.4) are not waste as well. 3. I propose my own view of the problem (table). Titles of classification categories (upper row) of the table are relative. We can name them not as types, class, category, etc. as it is done in the proposed variant. What is important is their hierarchy, consistency, complete account of all open burning categories. 4. I have no any additional proposals on sections 2.0, 3.0 and 4.0. Different prevention methods can be proposed for inclusion into them (prevention measures), technological control approaches to the by-products emission. Table Categories of open burning of production and consumption waste, natural resources and products as sources of POPs by-products Type Open burning of production and consumption waste, Natural resources, products in conditions favoring formation of POPs byproducts (low Subtype Open burning of production and consumption waste Kind Intended burning Class Homogeneous 51 Subclass Vegetation Category 1. Agricultural/crop residue 2. Land Clearing Debris). 3. Yard Waste(vegetation). 4. Burning of pressed dung for cooking and heating purposes Animal 5. Burning of animal carcasses Mineral (organomineral) Artificial (organic synthesis products) 6. Burning of sewer sludge 7. Waste water sediments 8. Agricultural Plastic 9. Tires. 10. Cable. Type temperatures, chlorine and organic substances presence) Subtype Open burning of natural resources Kind Class Mixed Unintended burning Mixed Intended burning Homogeneous Unintended burning Homogeneous Subclass 17. Landfills/dumps 18. Construction debris Vegetation 19. Savanna and forest Mineral (organomineral) 20. Petroleum gas flares at gas and oil fields in chloride class landscapes (ocean coast, sea and lake shores). 21. Forest and grassland fires. Vegetation Mineral (organomineral) Open burning of products Category 11. Household waste. 12. Medical waste. 13. Industrial non-hazardous waste. 14. Сonstruction/Demolition/Post disaster Debris 15. Automobile shredder fluff 16. Electronics waste 22. Crude Oil. 23. Oil well/Oil Spills Unintended burning Mixed 24. Vehicle fires 25. Fires in production areas and dwellings. Intended burning Mixed 26. Fireworks 27. Military Ordinance/Munitions. 52 COMMENTS SUBMITTED BY MR. HANS-PETER FAHRNI (SWITZERLAND) 53 54 55 COMMENTS SUBMITTED BY DR. HEIDELORE FIEDLER (UNEP) Dear Maria Cristina, I apologize for the delay with submission of my comments to the draft guidelines. Nevertheless, I hope that they will find entry into the existing guidance. My comments includes additional information for amendment of the present drafts and specific comments on individual documents and some comments related to several documents. For the first group of additional comments, I kindly ask you to forward the documents attached to this e-mail to the respective coordinators of documents; however, it should be taken into account that all papers issued by publishing companies are subject to copyright and cannot be put on the WebPage. Kind regards, Heidi Fiedler General comments on style and inconsistencies: - Apply abbreviations and acronyms as defined in the Stockholm Convention throughout all documents, e.g., PCDD/PCDF (and not PCDD/Fs, PCBs, etc.) throughout all text; - Note: the terms "dioxins" and "furans" are not used in the Stockholm Convention and, more important, they are wrong since these terms refer to other chemicals and not to PCDD and PCDF; - Note that UPOP(s) is not an agreed acronym. Personally, I do not like it. If considered to introduce an acronym for unintentional POPs, then it should be u-POPs; - Insert a blank between numbers and units (including %, °C); - Volumes have to be harmonized: the European and Asian authors use Nm³ (normal cubic meter) whereas the Canadian use Rm³ (Reference cubic meter). Since Nm³ is the wider used standardization (besides 25 EU countries also in the Aarhus POPs Protocol), I suggest to take Nm³ as the basis for these guidance documents; - Commonly used concentrations should be used throughout all documents: Stack concentrations should be given in ng TEQ/Nm³, ash or solids concentrations in ng TEQ/kg, concentrations in liquids in pg TEQ/L; - Limits of detection are not interesting to the chemists. Hat is meant here is limit of quantification (LOQ and not LOD); - The term "level" cannot be used when numeric values are given. 0.1 ng/Nm³ is a (mass) concentration and not a level. Subsequently, we have to talk about limit concentrations or limit values. If such numbers are legally binding or recommended does not matter. A law/directive/ordinance will make it legally binding whereas a guideline/orientation is only a reference and not legally binding; - All acronyms have to be introduced in text, including chemicals such as SO2, NH3, etc. Preferentially, each document should have a list of acronyms used, which may later be summarized into one list; - the apostrophe cannot be used when a plural is meant, e.g., POP's; - ppm is not a SI unit and should not be used; - AMESA is a trade name and should not be used as a generic term when referring to a continuous sampling method (there are others available that serve the same purpose; e.g., DioxinMonitoringSystems); Ref.: Consideration of Alternatives: I recognize that the text provided to define the borderlines of "alternatives" as agreed and requested in the mentioned conference call were not included into the draft. I kindly ask the coordinators to consider inclusion. Ref.: Residential combustion sources This document needs much input since there is almost no information included on PCDD/PCDF. The references given in the Toolkit for category 3 may be consulted. When listing various firing installations, categorization has to be made as to the type of the fuels especially to the physical state 56 (solid, liquid, gaseous) and to its purity. Addition of wastes to the fuels results in higher release of PCDD/PCDF which has been demonstrated in solid residues and stack emissions. I attach a publication summarizing some of the important findings: Lavric et al. (2004): Dioxin levels in wood combustion-a review. Biomass and Energy. The list of references should be taken into account for further reading. Biomass-Wood combustion_2003.p.. Ref.: Firing installations for wood and other biomass See the above paper by Lavric for additional information. Further reading include Materialien 172 of BUWAL <http://www.umweltschweiz.ch/imperia/md/content/luft/fachgebiet/f/feuerungen/10.pdf> Mohn et al. <http://www.empa-ren.ch/Internet-Files/Programm/Aktuelles/aktualitaeten/StatusSeminar/pdf-files/Mohn-J.pdf> Marutzky <http://www.wki.fraunhofer.de/projekte/abschluss08206.pdf> Dissertation <http://www.biblio.tu-bs.de/ediss/data/20010723a/20010723a.pdf> Finally, this presentation contains some interesting technical details <http://www.wtb.tue.nl/woc/ptc/education/4S600/Section4-combustionprinciples+emissions.pdf> Additional reading: - the inventory reports of Landesumweltamt Nordrhein-Westfalen on behalf of the EU provide information on performances of European plants, especially as additional information to the ferrous and non-ferrous metal sectors - both are available for download from the EU dioxin Website <http://europa.eu.int/comm/environment/dioxin/>: LUA (1997): Identification of Relevant Industrial Sources of Dioxins and Furans in Europe. Materialien No. 43. Landesumweltamt Nordrhein-Westfalen, Essen, 1997 LUA (2000): The European Dioxin Emission Inventory - Stage II. Final Report December 2000. Materialien No. 59. Landesumweltamt Nordrhein-Westfalen, Essen 2001 Other remarks: - Subsequently to the finalization of the documents, I suggest to take out of the individual documents issues that are common to many of the documents. This should be done to first save space and make the individual guidance better understandable and second to avoid contradictory statements/requirements. Examples include: handling of ashes from thermal processes, reporting and documentation, sampling and analysis; - in the same way, all flue gas cleaning technology can be summarized and listed in one document and afterwards referred to in the other documents; e.g., cement and waste incineration documents Dr. Heidelore Fiedler Scientific Affairs Officer UNEP Chemicals International Environment House 11-13, chemin des Anémones CH-1219 Châtelaine (GE) Switzerland Tel.: +41 (22) 917-8187; mobile: +41 (79) 477-0833 Fax: +41 (22) 797 3460 E-mail: [email protected] 57 COMPILATION OF SUBMISSIONS ON THE DRAFT GUIDELINES ON BAT AND GUIDANCE ON BEP RECEIVED BY THE STOCKHOLM CONVENTION SECRETARIAT COMMENTS SUBMITTED BY NGOS COMMENTS SUBMITTED BY THE AMERICAN FOREST & PAPER ASSOCIATION AMERICAN FOREST & PAPER ASSOCIATION GROWING WITH AMERICA SINCE 1861 Comments of the American Forest & Paper Association on: Section V.C. Guidance by source category: Annex C, Part II Source Categories “Production of pulp using elemental chlorine or chemicals generating elemental chlorine for bleaching” Draft of April 15, 2004 Preamble These comments are provided by the American Paper & Forest Association to assist the Expert Group in the development of Best Available Techniques and Best Environmental Practices for the elimination of specific polychlorinated dibenzo-pdioxins and polychlorinated dibenzofurans that may be formed during the bleaching of chemical pulp and emitted to waterways. ( AF&PA contact: Dr. John L. Festa). General Comments on “Draft Guidelines on BAT for production of pulp using elemental chlorine” The current, “Draft Guidelines on BAT for production of pulp using elemental chlorine” accurately identifies the relevant UPOPs that have the potential for formation when pulp is produced with elemental chlorine. The draft guidelines, with some exceptions noted below, describe the internationally recognized, scientifically sound, and widely implemented, Best Available Techniques for their reduction and elimination. Furthermore, the success of these Best Available Techniques has been well documented. Relevant international regulatory standards are also provided to guide Parties to the Stockholm Convention on Persistent Organic Pollutants toward implementation of the Convention. Section 1.3 Other sources of UPOPs in pulp mills Section 1.3 (1.3.1 – 1.3.5) is deficient in a number of respects: • • • The descriptions of the releases are general in nature; There is no description of the relevant UPOPs for each potential release; There is no discussion of mechanisms of formation or sources of contamination of the relevant UPOPs; 58 • There is no discussion of appropriate and demonstrated Best Available Techniques for reduction or elimination of relevant UPOPs; • There is no documentation of successful implementation of Best Available Techniques; and • There is no guidance provided to the Parties of relevant regulatory standards and the background upon which such standards are based. For these reasons AF&PA recommends this chapter be removed until each of the above noted issues has been fully addressed and supported by additional information, and/or required research, technology development and economical implementation. Section 2.2.1 Upstream and downstream aspects Section 2.2.1 while emphasizing bleaching processes where chlorine is still practiced, for the most part, discusses technology options for elimination of chlorinated organic compounds in general. Development of BAT/BET for elimination of chlorinated organic chemicals is clearly outside the scope of the treaty. For this reason alone, AF&PA recommends this chapter be removed from the guidelines. In addition, AF&PA believes this section should be removed based on the following summary. Since the late 1980s, the international scientific community has rigorously examined and rejected the hypothesis that the presence of and the amount of chlorinated organic substances is a measure of potential adverse environmental effects. More importantly, the scientific community has rejected the hypothesis that decreased chlorinated organic emissions will result in improved effluent quality and environmental protection. Overwhelming scientific evidence indicates these hypotheses are flawed for the following reasons: • Chlorinated organic compounds, as measured by the amount of chlorine attached to organic substances, is not a predictor of bioassay responses for either primary or secondary treated effluents1. • There are no established causal relationships between ecological effects and the concentration of chlorinated organic substances2. • Factors other than the presence or absence of chlorine containing organic substances determine ecological responses. Natural compounds extracted from wood in pulping processes and released to the environment have been identified as one likely cause. • Ecological responses to fish have been found downstream of mills with and without chlorine- and/or chlorine dioxide-based bleaching3. • Model ecosystem studies have shown no relationship between the concentration of chlorinated organic substance and observed environmental effects4. O’Connor, B.I., Kovacs, T.G., Voss, R.H. and Martel, P.H. A Study of the Relationship Between Laboratory Bioassay Response and AOX Content for Pulp Mill Effluents. Journal of Pulp and Paper Science: Vol. 19. No. 1. January 1993 2 Priha, M. Ecotoxicological Impacts of Pulp Mill Effluents in Finland. 1994 Proceedings International Fate and Effects of Pulp and Paper Mill Effluents Conference, Vancouver B.C. St. Lucie Press, Florida, (1996) 3 Williams, T.G., Carey, J.H., Burnison, B.K., Dixon, D.G., and Lee, H.-B. Rainbow Trout Mixed Function Oxygenase Responses Caused by Unbleached and Bleached Pulp Mill Effluents: A Laboratory Study. 1994 Proceedings International Fate and Effects of Pulp and Paper Mill Effluents Conference. Vancouver B.C. St. Lucie Press, Florida, (1996) 1 59 • Environmental effects assessed by field studies in receiving waters do not correlate with the concentration of chlorinated organic substances5. Finally, the discussion of technologies minimizing bleach plant effluent volume, delignification, enzyme pretreatment, chemical substitution, effluent treatment, sludge disposal and combustion processes while relevant in the development of overall environmental regulations for protection of the ecosystem, are not relevant in this BAT guideline for elimination of UPOPs. Specific Comments on “Draft Guidelines on BAT for production of pulp using elemental chlorine” Summary The last line of the second paragraph should be amended as follows: “… have been identified as potentially being produced ...” The next sentence should be amended as follows: “… can be taken for decreasing and/or eliminating …” The summary would benefit by adding the following to the measures that can taken for decreasing and/or elimination the formation of 2378-TCDD and 2378-TCDF: • • Maximize knot removal; Eliminate pulping of wood chips contaminated with polychlorinated phenol; and • Reduce application of molecular chlorine by decreasing active chlorine multiple. Section 1.2.1 Process Steps in general The third line should be amended as follows: “… residue cleaning and de-knotting …” Section 1.2.2 Pulping Methods Applied Something is missing at the end of the second paragraph; see the following: “… in the case of ? are continuous processes ? are vertical tower constant flow digesters …” The last line of the last paragraph should be amended as follows: Tana, J. and Lehtinen, K-J., The Aquatic Environmental Impact of Pulping and Bleaching Operations - An Overview. Finnish Environmental Agency, Helsinki, (1996). 5 Munkittrick, K.R., Servos, M.R., Carey, J.H. and Van Der Kraak, G.J. Environmental Impacts of Pulp and Paper Wastewater: Evidence for a Reduction in Environmental Effects at North American Pulp Mills Since 1992. IAWQ, 1996 Proceedings of the 5th Forest Industries Waste Water Symposium.Vancouver, B.C., June 1996. 4 60 “… it is achieved using non-chlorinated compounds such as dithionite or peroxides …” The use of the term “non-chlorinated” is unnecessary, as chlorine was never used for mechanical pulp bleaching. Section 1.2.2.3 Sulphite Pulping Processes The last sentence could be amended as follows: “… Sulphite pulps are relatively bright compared to kraft pulps and are also relatively easy to bleach with oxygen based chemicals such as peroxides …” The comment that they are easy to bleach without chlorine chemicals is not necessary. Section 1.2.3 Bleaching The first sentence of the third paragraph should be amended as follows: “… ECF pulp bleached with chlorine dioxide accounts for the predominant share of roughly three-quarters6 of the bleached pulp produced worldwide …” The last sentence of the third paragraph should be amended as follows: “… Roughly 20% of the bleached pulp produced world-wide is still bleached with some elemental chlorine…” In the preceding sentence, “some” need not be underlined. The emphasis is not necessary. Section 1.2.3.3 Elimination mechanisms for 2378-TCDD/F This section should be amended as follows: • The title of Figure 2 should be: “… 2378-TCDF formation with different chlorine dioxide substitution level” • The next sentence should be “… 2378-TCDD/F formation will be reduced and ultimately eliminated by increasing chlorine dioxide substitution …” • The next paragraph should be amended as follows: “… The summary effect of active chlorine multiple and chlorine dioxide substitution and precursor concentration can be seen in the figure 3. The level of the dioxin formation under these conditions, i.e., high active chlorine multiple and low chlorine dioxide substitution, is expected to vary depending on the DBD content of the brownstock …” • The title of Figure 3 should be: “… Effect of precursor content, active chlorine multiple and chlorine dioxide substitution level on 2378-TCDD formation …”. The figure does not show the effect of precursor content. • The last sentence of the next paragraph should be removed. The fact that ECF bleaching leads to the formation of a relatively small amount of chlorinated compounds is true but not relevant to the discussion of the elimination of 23786 Trends in World Bleached Chemical Pulp Production: 1990-2002. Alliance for Environmental Technology. December, 2002. 61 TCDD/F. The latter half of the sentence discussing 85% substitution is unclear and confusing. Section 1.3 Other sources of UPOS in pulp mills The title should be amended to “… Other sources of UPOPs in pulp mills …” Section 1.3 (1.3.1 – 1.3.5) is deficient in a number of respects: • • • The descriptions of the releases are general in nature; There is no description of the relevant UPOPs for each potential release; There is no discussion of mechanisms of formation or sources of contamination of the relevant UPOPs; • There is no discussion of appropriate and demonstrated Best Available Techniques for reduction or elimination of relevant UPOPs; • There is no documentation of successful implementation of Best Available Techniques; and • There is no guidance provided to the Parties of relevant regulatory standards and the background upon which such standards are based. For these reasons AF&PA recommends this chapter be removed until each of the above noted issues has been fully addressed and supported by additional information, and/or required research, technology development and economical implementation. Section 2.2.1 Upstream and downstream aspects Section 2.2.1 while emphasizing bleaching processes where chlorine is still practiced, for the most part, discusses technology options for elimination of chlorinated organic compounds in general. Development of BAT/BET for elimination of chlorinated organic chemicals is clearly outside the scope of the treaty. For this reason alone, AF&PA is of the opinion that this chapter should be removed from the guidelines. In addition, AF&PA recommends this section be removed based on the following summary. Since the late 1980s, the international scientific community has rigorously examined and rejected the hypothesis that the presence of and the amount of chlorinated organic substances is a measure of potential adverse environmental effects. More importantly, the scientific community has rejected the hypothesis that decreased chlorinated organic emissions will result in improved effluent quality and environmental protection. Overwhelming scientific evidence indicates these hypotheses are flawed for the following reasons: • Chlorinated organic compounds, as measured by the amount of chlorine attached to organic substances, is not a predictor of bioassay responses for either primary or secondary treated effluents7. • There are no established causal relationships between ecological effects and the concentration of chlorinated organic substances8. O’Connor, B.I., Kovacs, T.G., Voss, R.H. and Martel, P.H. A Study of the Relationship Between Laboratory Bioassay Response and AOX Content for Pulp Mill Effluents. Journal of Pulp and Paper Science: Vol. 19. No. 1. January 1993 8 Priha, M. Ecotoxicological Impacts of Pulp Mill Effluents in Finland. 1994 Proceedings International Fate and Effects of Pulp and Paper Mill Effluents Conference, Vancouver B.C. St. Lucie Press, Florida, (1996) 7 62 • Factors other than the presence or absence of chlorine containing organic substances determine ecological responses. Natural compounds extracted from wood in pulping processes and released to the environment have been identified as one likely cause. • Ecological responses to fish have been found downstream of mills with and without chlorine- and/or chlorine dioxide-based bleaching9. • Model ecosystem studies have shown no relationship between the concentration of chlorinated organic substance and observed environmental effects10. • Environmental effects assessed by field studies in receiving waters do not correlate with the concentration of chlorinated organic substances11. • Finally, the discussion of technologies minimizing bleach plant effluent volume, delignification, enzyme pretreatment, chemical substitution, effluent treatment, sludge disposal and combustion processes while relevant in the development of overall environmental regulations for protection of the ecosystem, are not relevant in this BAT guideline for elimination of UPOPs. Section 3 Performance standards Under 2378-TCDD/2378-TCDF ppq To Water and the USA Ammonium based and specialty sulphite, the measurement point is: “… in bleach plant effluent…” Section 4 Performance Reporting The final sentence of the first full paragraph should be amended as follows: “… The testing period reverts back to monthly testing if either a quarterly test or an annual test detects dioxins or furans exceeds the level of quantitation (LOQ) … “ Williams, T.G., Carey, J.H., Burnison, B.K., Dixon, D.G., and Lee, H.-B. Rainbow Trout Mixed Function Oxygenase Responses Caused by Unbleached and Bleached Pulp Mill Effluents: A Laboratory Study. 1994 Proceedings International Fate and Effects of Pulp and Paper Mill Effluents Conference. Vancouver B.C. St. Lucie Press, Florida, (1996) 10 Tana, J. and Lehtinen, K-J., The Aquatic Environmental Impact of Pulping and Bleaching Operations - An Overview. Finnish Environmental Agency, Helsinki, (1996). 11 Munkittrick, K.R., Servos, M.R., Carey, J.H. and Van Der Kraak, G.J. Environmental Impacts of Pulp and Paper Wastewater: Evidence for a Reduction in Environmental Effects at North American Pulp Mills Since 1992. IAWQ, 1996 Proceedings of the 5th Forest Industries Waste Water Symposium.Vancouver, B.C., June 1996. 9 63 COMMENTS SUBMITTED BY ARNIKA ASSOCIATION –TOXICS AND WASTE PROGRAMME Comments on „Draft guidelines and guidance on BAT and BEP for the sources of dioxins and other unintentionally produced POPs identified in Annex C of the Stockholm Convention“ The submitted „Draft guidelines and guidance on BAT and BEP for the sources of dioxins and other unintentionally produced POPs identified in Annex C of the Stockholm Convention“ (quoted as „Draft guidelines and guidance on BAT and BEP“ further) will undoubtedly represent an important document for parties of the Stockholm Convention. This document should serve in particular to fulfilment of the requirements of the Stockholm Convention which requires: „…each country to reduce the total releases derived from anthropogenic sources of [POPs], with the goal of their continuing minimization and, where feasible, ultimate elimination.” Annex C of the Stockholm Convention further states: “When considering proposals to construct new facilities or significantly modify existing facilities using processes that release chemicals listed in this Annex [i.e. dioxins, furans, PCBs and HCB], priority consideration should be given to alternative processes, techniques or practices that have similar usefulness but which avoid the formation and release of such chemicals.” (Annex C, Part V (B)(b)) When reviewing the „Draft guidelines and guidance on BAT and BEP“ from the point of view of the two above-mentioned quotations of the text of the Convention, it has to be stated that the Draft is not in accordance with them or it does not fulfil even a half of them. For this reason, we require revision of the Draft. Specifically, in the case of incineration of wastes, either in incinerators or in cement kilns, an important part is avoidance of these practices. The description of the Best Environmental Practice should contain also a description of the specific sources included into Part V. Therefore, in the case of incineration of municipal wastes, we lack description of methods used in the cities and states which adopted „Zero waste“ policy as their waste management policy. The Australian city Canberra could serve as an example for a description of such method. Similarly, in the case of description of medical waste incineration, we lack a more detailed description of alternative methods of medical waste treatment. The comprehensive report prepared by Health Care Without Harm network „Non-Incineration Medical Waste Treatment Technologies“ can be used as a source for such description. We recommend to do this when revising the „Draft guidelines and guidance on BAT and BEP“. One of the important methods resulting in reduction of POPs releases is, for example, elimination of PVC, as a material comprising chlorine, from the waste which is incinerated or deposited into landfills. Incineration of PVC and other chlorinated substances results in higher likelihood of POPs formation, as proved by numerous studies. Therefore, we hope that recommendation to eliminate PVC, and, optionally, further materials, from the flow of wastes into incinerators and landfills, will be incorporated into the „Draft guidelines and guidance on BAT and BEP“. From our point of view, BEP in the case of PVC is reduction of its use with the goal of its total replacement. In the countries which have experience with introduction of full informing of the public about flows of toxic chemicals through publicly available Pollutant Release and Transfer Register, reduction of all toxic chemicals releases is evident. For this reason, we believe that the list of BEP in the „Draft guidelines and guidance on BAT and BEP“ should include also establishment of PRTRs. From this point of view, recommendation to the parties of the Convention to adopt PRTR Protocol to Aarhus Convention should be considered. The „Draft guidelines and guidance on BAT and BEP“ reflect, to a certain extent, loopholes in „The Standardized Toolkit for Identification and Quantification of Dioxin and Furan Releases“, or more precisely, its shortcomings concerning releases of other unwanted by-products (PCBs and HCB), and 64 in the field of assessment of the content of unwanted by-products in solid and liquid residues. We lack such assessment in the part dealing with incineration of wastes in cement kilns. If HCB is formed during incineration of hazardous wastes in incinerators, then certain emissions of this chemical can be expected also during incineration of wastes in cement kilns as it was measured in Poland (see further detail comments). It is not possible to be satisfied with the statement that the emissions of HCB and PCB are not subject to regulatory monitoring in cement plants. All technologies, including incineration of hazardous wastes (both in incinerators and in cement kilns), plasma arc, pyrolysis and others should be compared according to their Destruction Efficiencies in full TEQs scale, in the „Draft guidelines and guidance on BAT and BEP“. Therefore the following part is specifically focused on POPs waste destruction. Criteria for destruction of POPs waste Parties are to take measures according to the Stockholm Convention so that POPs wastes are: ∼ ∼ Disposed of in such a way that the persistent organic pollutant content is destroyed or irreversibly transformed so that they do not exhibit the characteristics of persistent organic pollutants... …not permitted to be subject to disposal operations that may lead to recovery, recycling, reclamation, direct reuse or alternative uses for POPs. Criteria from Stockholm Convention: A suitable destruction process/technology therefore should: ∼ ∼ ∼ ∼ Prevent the formation of dioxins, furans and other by-product POPs. Prevent the release of dioxins/furans and other by-product POPs. Not generate any wastes with POPs characteristics. Not utilise any POPs disposal methods which are non-destructive, such as landfilling or recycling in any form. By undersigned NGOs endorsed criteria for destruction of (historical) POPs waste originally prepared by Greenpeace: • • An effective destruction efficiency of 100% - taking into account all inputs and releases; Complete containment of all process streams to enable testing and reprocessing if necessary to ensure; • No uncontrolled releases from the process. Further Considerations when evaluating technologies: • • • • Eliminate inappropriate technologies (based on guidance/criteria) – E.g. formation of POPs/releases of POPs/POPs wastes/landfill etc Destruction Efficiency (based on inputs vs. all outputs) Ability to contain all process streams Ability to reprocess materials, residues, gases, liquids if required 65 • • • • • Availability of complete process information (analytical data) Track record/commercial availability Safety/OH&S Hazardous materials use Community acceptability We prefer to use a concept of Destruction Efficiency rather than Destruction and Removal Efficiency commonly used during the evaluation of technologies for POPs destruction. Difference between these two concepts is quite clear from paper prepared by D. Luscombe as Greenpeace factsheet (NonIncineration Technology Fact Sheet #2). Few detail comments In Section V.B. “Cement kilns firing hazardous waste”, Table 1: “Summary of PCDD/PCDF measurements data” is contained. This Table attempts to summarise the measured concentrations of PCDD/PCDF in flue gases. There were done measurements on cement kilns co-burning waste as fuel in the Czech Republic in 2002 - 2003. Only in one case a level of 0.005 ng I-TEQ/m3 was measured. The rest of results (12 measurements together) were in a range of 0.023 - 2.3 ng I-TEQ/m3. In three cases, the results exceeded the limit of 0.1 ng I-TEQ/m3. Measurements done in Poland in a cement kiln co-incinerating non-hazardous waste found that emissions of PCBs and HCB rose many times in comparison with a cement kiln burning coal only, what is contrary to statement in chapter 3.4 of Section V.B. of the „Draft guidelines and guidance on BAT and BEP“: “However, some measurements have revealed that HCB could not be detected, i. e. HCB emissions is most probably not an issue for the cement industry.” Cement kiln Co-incinerating waste Burning coal PCDD/F ng-TEQ/m3 0.070 0.055 PCBs ng-TEQ/m3 8.95 4.45 HCB ng-TEQ/m3 44.2 2.90 Ref.: Grochowalski A., Sprawozdanie z przeprowadzonych pomiarow i oznaczania stezenia PCDDs/PCDFs, HCB i PCBs, 30.09.2002; http://ks.ios.edu.pl/gef/doc/GF-POL-INV-R1.PDF Comment to Section V.B., chapter 3. Process Outputs: Recycling cement kiln dust (CKD) directly to the kiln generally results in a gradual increase in alkali content of generated dust that may damage cement kiln linings, produce inferior cement, and increase particle emissions.i In Europe, CKD is commonly added directly to the product cement.ii This practice may well explain the PCDD/PCDF levels of 5.1 to 17.8 ng I-TEQ/kg in clinker that has been reported by Denmark,iii since PCDD/PCDF levels as high as 297 ng I-TEQ/kg are known to occur in CKD.iv Elevated PCDD/PCDF levels in CKD suggest that fugitive emissions of CKD constitute significant releases of PCDD/PCDF. Fugitive emissions of CKD associated PCDD/PCDF occur not only with operation of kilns but also subsequent handling, storage and disposal of CKD. For example, the Environmental Protection Agency offered the following evaluation:v may and with U.S. Additionally, particulate emissions of fugitive dust are the major contributor of CKD to EPA's indirect foodchain pathway model. The Agency's quantitative modeling of ``indirect'' food chain pathways, both aquatic and agricultural, indicates potential human health effects, both cancer and non-cancer. A wide range of chemical constituents, including arsenic, cadmium, chromium, barium, thallium, lead, and dioxins, were indicated as constituents of concern at various plants. Because some CKD disposal units are located near, and in some instances immediately adjacent to, farm fields, rural residences with gardens, or surface waters containing fish, there is potential 66 for indirect risk from the consumption of CKD-contaminated beef, vegetables and fish, as well as ingestion of CKD-contaminated water during recreational swimming. In Section V.A.1. “Municipal and hazardous waste, and sewage sludge”, there is stated in Table 6.3 that by incinerating 1 tonne of MSW, 210 kg of bottom ash is produced. In the Czech MSWI it is up to 370 kg according to records from the MSWI Termizo Liberec. You can find more detailed data from Poland useful for medical waste incineration guidelines in section V.A.2. in Annex to our Comments. Conclusions As follows from the previous text, we require completion, or, optionally, revision of the „Draft guidelines and guidance on BAT and BEP“ in order to contain: - „Zero waste“ policy examples as realistic alternative to municipal waste incineration avoiding new POPs releases generated by waste incineration and/or by fires on landfills; - more detailed description of alternatives to incineration of medical wastes; - more detailed description of alternatives to incineration of hazardous wastes; - separate dealing with incineration of hazardous wastes in the „Draft guidelines and guidance on BAT and BEP“, because this is a waste different in many aspects from municipal waste; - more detailed description of chemical treatment of fly and boiler ashes, resulting in decomposition of POPs; - comparison of all technologies by means of Destruction Efficiencies based on full TEQ and/or all POPs releases assessment; - reduction of PVC and other substances, incinerating of which, or, optionally, firing of which on landfills, or in the case of which household and/or open burning of waste leads to POPs releases; - establishment of publicly available PRTRs incorporating full information on POPs in all recorded flows, as information systems which, in its consequence, result in reduction of releases of toxic chemicals in general. These comments were endorsed by following NGOs and experts: Ing. Milan Havel, Ing. Petr Hrdina and RNDr. Jindrich Petrlik, Arnika Association, Czech Republic Dr. Mahmood A. Khwaja, Sustainable Development Policy Institute (SDPI), Islamabad. Pakistan Pawel Gluszynski, Waste Prevention Association - 3R, Krakow, Poland Boryana Hrissimova, independent environmental expert, Sofia, Bulgaria Ralph Ryder, Communities Against Toxics, United Kingdom Dr. Paul Connett, Professor of Chemistry, St. Lawrence University, Canton, NY, USA Ellen Connett, Editor, Waste Not, Canton, NY, USA Huub Scheele, Both ENDS, Amsterdam, The Netherlands 67 Ing. Cestmir Hrdinka, Executive director, Health Care Without Harm Europe, Prague, Czech Republic (undersigning the comments related to medical waste) Donald L. Hassig, Director, Cancer Action NY, USA Eugeniy Lobanov, Foundation for Realization of Ideas (FRI), Belarus Igor Hadjamberdiev "PAN Central Asia network" Kyrgyzstan-Uzbekistan-Tadjikistan Miroslav Beranek, Czech Ecological Society, Czech Republic Sonia S. Mendoza, President, Mother Earth Foundation, Philippines Vratislav Bina, Civic Association Suchomasty, Czech Republic Any reactions please send to: Arnika Association - Toxics and Waste Programme Chlumova 17 130 00 Praha 3 Czech Republic tel. and fax number: + 420 222 781 471 e-mail: [email protected] ANNEX: Table 1. Non-incineration medical waste treatment technologies certified for the Polish market: G.P.P.U. (Polish) Ecodas (French) Meteka (Austrian) Newster (Italian) Sintion (Austrian) Chemical Autoclave + Thermal Microwave Treatment Sintion 1.1. Newster 10 Installation Autoclave TSO 150 Autoclave T.300 Microwave Medister 360 Level sterilisation sterilisation sterilisation sterilisation sterilisation Maximum quantity [TPA] * 350 300 130 370 **120 Capacity [kg/cycle] 70 35 12 – 18 10 – 25 12 Chamber capacity [m ] 0,93 0,35 0,06 0,13 0,103 Installation dimension L x W x H [m] 2,4x1,5x2,7 1,85x2,1x3 1,7x1,05x0,8 Installation mass [kg] 3150 2000 480 1100 430 Power supply type [V] 3 x 380 380 3 x 380 3 x 380 3 x 400 11,2 17 no data 30 no data 166 000 € 130 000 € 70 000 € 85 000 € 50 000 € 3 Power [kW] Price net [excluding VAT] 68 1,2x0,8x1, 0,84x1,2x1,1 4 G.P.P.U. (Polish) Ecodas (French) Meteka (Austrian) Newster (Italian) Sintion (Austrian) without steam generator without steam generator yes yes yes 24 – 36 12 12 12 12 - 18 Water use per cycle [m3] 0,25 0,1 0,05 0,15 – 0,3 no data Steam use per cycle [kg] 30 15 – – – Energy use per cycle [kWh] 5 3 8,5 0,6 1 none The price includes all equipment Term of guarantee [month] Chemical use per cycle [kg] Cycle time [minute] Shredder Chamber unload none none 40 – 90 40 – 60 55 15 – 25 10 – 30 yes yes no yes no automatic manual ~ 90 < 50 automatic Waste temperature right after process [oC] * ** none 0,3 – 0,5 {14 – 15% NaClO} gravitational gravitational 80 - 100 80 50 Maximum cycle time, and full load; operational for 7466 hours per year (85%). Sintion requires 8 hours break per twenty-four hours. Investment costs recalculated for maximum capacity [€ net/tonne] 2000 1500 512 474 433 500 Newster Ecodas G.P.P.U. Outdated incinerator 229 Modern incinerator 0 538 416 Sintion 683 Meteka 1000 Modern incinerator: equipped with secondary chamber; filters and scrubber, and automatic monitoring control system as required by Directive 2000/76/EC. [Average price based on three proposed installations, in 2002/2003.] 69 Outdated incinerator: equipped with secondary chamber; filters and scrubber, without automatic monitoring control system as required by Directive 2000/76/EC, and [possibly] not meeting the EU emission standard. [Average price based on seven installations built in late 90’s.] All incinerators have average capacity 300 kg/h. Source: Urządzenia do unieszkodliwiania zakaźnych odpadów medycznych i weterynaryjnych dostępne na rynku krajowym [Medical waste treatment technologies available on the Polish market], OTZO/WPA, Kraków, March 2003. ___________________________________ i U.S. Environmental Protection Agency, 1998. Technical Background Document on Ground Water Controls at CKD Landfills. Draft. Washington, D.C.: Office of Solid Waste, U.S. Environmental Protection Agency. ii Lohse, J., Wulf-Schnabel, J., 1996. Expertise on the Environmental Risks Associated with the Co-Incineration of Wastes in the Cement Kiln "Four E" of CBR Usine de Lixhe, Belgium. Hamburg, Germany: Okopol. http://www.oekopol.de/Archiv/Anlagen/CBRBelgien.htm iii Hansen, E., 2000. Substance Flow Analysis for dioxins in Denmark. Environmental project No. 570. Copenhagen, Denmark: Danish Environmental Protection Agency. iv U.S. Environmental Protection Agency, 1998. Draft Risk Assessment for Cement Kiln Dust Used as an Agricultural Soil Amendment. Draft Report. Washington, D.C.: Office of Solid Waste, U.S. Environmental Protection Agency, 16 June 1998. v U.S. Environmental Protection Agency, Standards for the Management of Cement Kiln Dust; Proposed Rule. 40 CFR Parts 259, 261, 266, and 270. Federal Register: August 20, 1999 (Volume 64, No. 161, pp. 45631-456971. 70 COMMENTS SUBMITTED BY CANADIAN STEEL PRODUCERS ASSOCIATION Comments on the Draft Guidelines on Best Available Techniques (BAT) Relevant to Article Five and Annex C of the Stockholm POPs Convention Submitted by the Canadian Steel Producers Association ♦ Draft guidelines have been prepared on a number of sources not identified in Annex C to the Stockholm Convention. This includes secondary lead production, primary aluminiun production, magnesium production, secondary steel and primary metals. No rationale is presented as to why they have been included, nor was there any consultation before the documents for these sources were prepared. Only those sources cited in Annex C of the Convention should be included in the preparation of draft Guidance on BAT/BEP. ♦ The table of contents lists sections on how to use the guidelines and guidance with the indication that they are yet to be developed. This content of this section is an important part of the guidelines and it should clearly indicate that these documents are “guidance” that offers a range of approaches for jurisdictions and industrial sectors. The fact that the documents represent guidance should be clear in the language and tone of the Guidelines. It would be appropriate to indicate at the beginning of the discussion for each source that the techniques and practices most appropriate to a specific industrial source will be affected by considerations specific to an industry and jurisdiction, and will be affected by competitive and cost considerations. ♦ The language used in a number of the guidance documents dealing with the various metals sectors goes beyond guidance in dealing with areas such as achievable levels and monitoring and reporting. It is appropriate to indicate an achievable level of emissions based on experience from a range of countries, but schedules for reaching them should be the decision of the appropriate jurisdiction. Again, it is appropriate to recommend a monitoring program that meets accepted criteria and reporting of results, but the frequency of testing and details related to any program should again be the decision of the responsible jurisdiction. This is the approach adopted in the guidance document for Chemical Production Processes. ♦ In best available techniques, available is clarified to mean “those techniques that are accessible to the operator and that are developed on a scale that allow implementation in the relevant industrial sector, under economically and technical viable conditions, taking into consideration the costs and advantages”. This is not reflected in certain statements in the draft guidelines, for example on page 12 of the Draft Guidance for Secondary steel production, which states that “it should be feasible for all plants to implement some or all of the pollution prevention practices identified below”, without any discussion of the costs of implementing the measures. ♦ All guides should be reviewed to ensure consistency from the perspective of what is covered and how specific items are handled (see third bullet above). 71 COMMENTS SUBMITTED BY CANCER ACTION CANCER ACTION NY www.canceractionny.org Cancer Prevention by Pollution Minimization 5/27/04 James B. Willis, Executive Secretary Stockholm Convention United Nations Environment Programme 11-13 chemin des Anemones CH-1219, Chatelaine, Geneva, Switzerland Dear Executive Secretary Willis, Cancer Action NY submits the following comments upon the Expert Group on BAT/BEP guidance on open burning of waste. In Section 1.0 of the guidance, it is stated: “Countries should work diligently to establish and implement sound practices including resource reduction, reuse, recycling, composting, modern sanitary landfilling, and BAT incineration.” Comment No.1. BAT incineration should not be included as an alternative to open burning of wastes due to the fact that environmentally significant levels of dioxins and dioxin-like compounds are created and released by the most carefully regulated incineration. Non-combustion disposal techniques and technologies should be the only recommended alternatives to open burning. In Section 1.1, it is stated: “In the short term, where there are not realistic alternatives to open burning, practical process modifications that are likely to reduce unintentional POPs generation include:4 • • • • • Reduction in the amount of material discarded via open burning. Consistent with the convention, this is the first line of improvement. Removal of non-combustibles, including glass and bulk metals, and materials of low fuel value. Supply of sufficient air Steady burning or rate of mass loss Minimization of smoldering, possibly with direct extinguishments” Comment No. 2. Removal of PVC plastics from the waste to be disposed of by open burning should also be recommended. PVC plastic smolders in an open fire. Smoldering, sooty combustion is a significant source of dioxins and dioxin-like compounds. In the following sections: 3.1.2, 3.1.3, and 4.1.3, BAT incineration is recommended as an alternative to the open burning of wastes. Comment No. 3. Please see Comment No. 1. In Section 4.2.4, it is stated that efficient combustion of shredded tires has been demonstrated in cement kilns, wood and coal combustors. Comment No. 4. Regardless of how efficient the combustion of shredded tires is for producing heat energy, emissions from this fuel use are relatively high in particulates. The most environmentally sound disposal method for waste tires is incorporation into road surfacing materials. 72 General Comments Comment No. 5. No mention is made in the guidance of the importance of public health education to the elimination of open waste burning. In many areas where open waste fire disposal takes place there exist numerous public health entities, including: local, regional and national public health departments. Residents are more inclined to change behaviors based upon warnings of adverse health effects, which come directly from government health agencies rather than from other sources such as environmental groups or government planning offices. Elimination of the open burning of wastes is the responsibility of government as a matter of public health protection. Dioxin exposure, which takes place by way of consumption of animal fat foods, imposes a significant cancer risk upon the residents of industrialized nations. The US Environmental Protection Agency (US EPA) has published a dioxin reassessment, which includes, “Part III: Integrated Summary and Risk Characterization for 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) and Related Compounds”. This document provides a quantification of dioxin exposure cancer risk. Epidemiologic studies of several exposed groups: workers who manufactured or applied dioxin contaminated pesticides, including pentachlorophenol, and 2,4,5-T; victims of an industrial accident in Seveso, Italy, which released kilogram quantities of dioxin; and US Air Force personnel engaged in Project Ranch Hand, the spraying of Agent Orange during the Vietnam War, demonstrate a linear relationship between dioxin exposure and increased cancer risk. According to US EPA, the average American consumes a quantity of animal fat sufficient to impose a dioxin and dioxin-like compound exposure of 1 pg dioxin TEQ/kg bw/day. This level of exposure is associated with a 1 in 1000 excess risk of developing cancer. Doubling one’s intake of animal fat food results in a doubled cancer risk. During the 1970s and 1980s, dioxin and dioxinlike compound levels in animal fat foods were considerably higher than current levels. Those who consumed animal fat produced over that time period have a significantly higher lifetime cancer risk; 1 in 100 represents a reasonable estimate of cancer risk for this group. Comment No. 6. Labeling of animal fat foods for dioxin and dioxin-like compound content constitutes a powerful educational tool for increasing public awareness of the need to eliminate the burning of waste in open fires. The consumer will seek out information on the source of this contamination. A public thus informed will support governmental policies implemented for the establishment of environmentally sound waste disposal practices. Thank you for this opportunity to contribute to the development of BAT/BEP guidance that will lead to the elimination of open waste burning as a source of the releases of dioxins and dioxin-like compounds to the environment. Respectfully submitted, Donald L. Hassig, Director Cancer Action NY Board of Directors: Frederick E. Biggs, Patricia M. Biggs, and Lewis M. Shepard Director, Donald L. Hassig 531 CR 28, Ogdensburg, NY 13669 [email protected] 73 CANCER ACTION NY www.canceractionny.org Cancer Prevention by Pollution Minimization June 10th, 2004 James B. Willis, Executive Secretary Stockholm Convention United Nations Environment Programme 11-13 chemin des Anemones CH-1219, Chatelaine, Geneva, Switzerland Re: Comments upon the Expert Group on BAT/BEP guidance on Waste Incinerators: Municipal and Hazardous Waste, and Sewage Sludge Dear Executive Secretary Willis, Cancer Action NY submits the following comments upon the Expert Group on BAT/BEP guidance on Waste Incinerators: Municipal and Hazardous Waste, and Sewage Sludge. This guidance needs to include a fully developed protocol for guarding against illegal fuel use. Unauthorized fuels can lead to significant increases in dioxin and dioxin-like compound formation. Inspection of waste, which is addressed in the guidance, is an important part of obtaining information about what is actually being burned. Records of all inspections should be maintained at the facility, and also provided to the government regulatory entity responsible for environmental protection. The public should have full access to these records. Due to the fact that inspection yields only sporadic snapshots of waste composition, additional means for determining what materials are being incinerated must be incorporated into the protocol. Testing of bottom ash for metals concentration will provide necessary information about fuel use. If fuel usage changes to include materials with a higher copper and/or iron content, dioxin emissions will increase due to the catalytic effect of these metals on dioxin formation. Such a change in fuel can be readily detected by ash testing. Incinerator bottom ash should be tested regularly for copper and iron concentrations. If it is discovered that these metals are present in the fuel over a considerable range of concentrations, it will be necessary to stack test when the higher metal content fuel is in use to determine how great an impact this fuel has on dioxin emissions. An ash testing protocol can serve as a deterrent to the burning of unauthorized waste materials. Only by following the protocol described above is it possible to accumulate the data that would be necessary to enforce fuel use restrictions. Without fuel use restrictions, dioxin and dioxin-like compound emissions will vary significantly from stack test results, thereby making the true emissions of the facility greater than what stack testing would indicate. Thank you for this opportunity to provide input on the development of the incineration guidance. Respectfully submitted, Donald L. Hassig, Director Cancer Action NY Board of Directors: Frederick E. Biggs, Patricia M. Biggs, and Lewis M. Shepard Director, Donald L. Hassig 531 CR 28, Ogdensburg, NY 13669 [email protected] 74 COMMENTS SUBMITTED BY THE FINNISH FOREST INDUSTRIES From: Luukko Kari [mailto:[email protected]] Sent: Wednesday, June 23, 2004 11:54 AM To: Cristina Cardenas Cc: [email protected] Subject: comments to the 2nd draft Dear receiver, Enclosed please find the Finnish forest industries' comments to the UNEP draft document "Guidelines on BAT for production of pulp using elemental chlorinE". Best Regards, <<Draft2 Comments 11.6.2004.doc>> Kari Luukko Mr. Kari Luukko Research Manager, Dr. Tech. Finnish Forest Industries Federation P.O. Box 336 (Snellmaninkatu 13) FIN-00171 Helsinki FINLAND tel. +358 (0)9 132 6622, +358 (0)40 565 6622 fax. +358 (0)9 132 4445 mailto: [email protected] 75 2 nd DRAFT GUIDELINES ON BAT FOR PRODUCTION OF PULP USING ELEMENTAL CHLORINE OR CHEMICALS GENERATING ELEMENTAL CHLORINE FOR BLEACHING SUMMARY ..................................................................................................................................... 77 1 INTRODUCTION..................................................................................................................... 77 1.1 GENERAL INFORMATION ABOUT PULP AND PAPER INDUSTRY ................................................... 77 1.2 PROCESS DESCRIPTION ........................................................................................................ 78 1.2.1 Process Steps in general ............................................................................................ 78 1.2.2 Pulping Methods Applied............................................................................................. 78 1.2.2.1 The Kraft (Sulphate) Pulping Process ..................................................................... 79 1.2.2.2 Lime and Soda processes ....................................................................................... 81 1.2.2.3 Sulphite Pulping Processes..................................................................................... 81 1.2.3 Bleaching..................................................................................................................... 82 1.2.3.1 Bleaching with chlorine and hypohlorous acid......................................................... 82 1.2.3.2 Formation of 2378-TCDD/F .................................................................................... 83 1.2.3.3 Elimination mechanisms for 2378-TCDD/F ............................................................. 84 1.3 OTHER SOURCES OF UPOS IN PULP MILLS............................ ERROR! BOOKMARK NOT DEFINED. 1.3.1 Releases to water from recycled fibre processing......... Error! Bookmark not defined. 1.3.2 Releases from process sludges. ................................... Error! Bookmark not defined. 1.3.3 Releases to air from burning of organic materials in the recovery cycle to generate energy and recover inorganic process chemicals...... Error! Bookmark not defined. 1.3.4 Releases to air from burning wood and biomass to generate energyError! Bookmark not defin 1.3.5 Releases / Transfer into products (pulp or paper)......... Error! Bookmark not defined. 2 BEST AVAILABLE TECHNIQUES (BAT) FOR PRODUCTION OF PULP USING ELEMENTAL CHLORINE .............................................................................................................. 86 2.1 PRIMARY MEASUREMENTS ..................................................................................................... 86 2.2 SECONDARY MEASUREMENTS ............................................................................................... 86 2.2.1 Upstream and downstream aspects.............................. Error! Bookmark not defined. 3 PERFORMANCE STANDARDS ............................................................................................ 87 4 PERFORMANCE REPORTING.............................................................................................. 88 References 76 Draft Guidelines on BAT for production of pulpusing elemental chlorine or chemicals generating elemental chlorine for bleaching Summary Annex C Part II (c) of the Convention identifies ”production of pulp using elemental chlorine or chemicals generating elemental chlorine” as an industrial source category having ”the potential for comparatively high formation and release of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/PCDF), hexachlorobenzene (HCB), and polychlorinated biphenyls (PCB).” Of these compounds HCB and PCB are not formed during pulp bleaching. Only polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/PCDF) have been identified as being unintentionally produced during the production of pulp using elemental chlorine. Of the 17 PCDD/PCDF congeners with chlorine in the 2,3,7 and 8 positions, only two congeners, namely 2,3,7,8-tetrachlorodibenzo-p-dioxin (2378-TCDD) and 2,3,7,8-tetrachlorodibenzofuran (2378-TCDF), have been identified as potentially being produced during chemical pulp bleaching using chlorine. As a summary, the following primary measures can be taken for eliminating or decreasing the formation of 2378-TCDD and 2378-TCDF: • • Eliminate elemental chlorine via replacing with chlorine dioxide (ECF bleaching), or with chlorine free chemicals (TCF bleaching) Reduce application of elemental chlorine via decreasing chlorine multiple or increasing substitution of chlorine dioxide for molecular chlorine Introduction General information about pulp and paper production Pulp and paper are manufactured from wood, recycled paper and many types of agricultural residue. Wood and the main non-wood materials used in papermaking are a complex mixture of the same substances – cellulose (40-45%), hemicelluloses (25-35%), lignin (20-30%) and extractives (2-15%). Most ligno-cellulosic and cellulosic materials of fibrous structure may be processed into various grades of papers and paperboard. Fibres from different raw materials are, however, not alike. They differ considerably in their morphological and chemical characteristics, which make them more or less suitable for papermaking. Pulping and bleaching technology must be matched to the quality and characteristics of the pulp and paper grades to be produced. No single pulping or bleaching process can produce pulp suitable for all uses. For instance, newsprint is a high volume product of moderate strength, opacity and printability and a relatively short life. Therefore, a high yield of pulp at the expense of maximum achievable strength and brightness can be manufactured from the raw materials and there is a lower bleaching requirement due to natural brightness of the pulps. On the other hand packaging papers need strength if they are to be fit for use and here it is necessary to accept a lower yield via a different manufacturing route in order to obtain this 77 strength but again the bleaching requirement may be low if this is a middle layer board . Further characteristics such as the brightness and its durability as required by outer packaging layers and printing and writing papers that may need to last for many years without yellowing, mean that and here the level of delignification and bleaching applied may need to be high. The amount of effort needed in bleaching can therefore vary widely. Apart from hardwood and softwood species normally used in pulping, in some parts of the world a very high proportion of primary cellulose fibres originate from nonwood raw materials such as bagasse, cereal straw, bamboo, reeds, grasses, jute, kenaf, flax and sisal [TAPPI, 1987]. Over 10% of world pulp production is made from these non-wood fibres and in some countries it is the dominant fibre source, for instance in China and India. Pulp and paper mills may be integrated or non-integrated. Non-integrated pulp mills (market pulp) are only manufacturing pulp that is then sold on the open market. Nonintegrated paper mills use purchased pulp for their paper production. In integrated pulp and paper mills, the activities of pulp and paper making are undertaken on the same site. With recovered paper manufacturing the level of integration is high; nearly all recovered paper mills include recovered paper processing, some of them adding purchased pulp. Compared to pulp production a relatively high number of small and medium-sized paper manufacturing facilities are in operation in many countries. A difference in relation to the scale of production is seen in different parts of the world with the capacities ranging from small mills of a few tens of tonnes per day through to major industrial complexes processing 1,000 to 1,500 tonnes per day. Process Description Process Steps in general The main processes involved in making pulp, cellulose and paper products are: raw material handling and preparation, such as transport, storage, wood debarking, chipping and agricultural residue cleaning and de-noding; then pulping; pulp processing and bleaching and finally paper or paperboard making. Cellulose rich pulp products are also manufactured as raw material for other industrial processes, the manufacture of rayon, cellophane and some products in the chemical industry for example. The industry is a divergent production process and so there is a wide range of techniques, using different pulping chemicals and process conditions as well as different bleaching sequences, that deliver the desired fibre product characteristics from a range of available raw fibre types and mixtures. The methods employed vary across the world both in relation to the characteristics of the fibre types available, the products to be made from them and the local pollution control restrictions that apply. Pulping Methods Applied 78 The manufacture of pulp uses mechanical, thermomechanical, chemimechanical and chemical methods. Mechanical and thermomechanical methods are used in integrated mills to make naturally bright, high yield pulps mainly used for newsprint manufacture. Chemical pulping methods are used in integrated and non integrated pulping mills. Pulps produced in different ways have different properties that make them suited to particular products. Pulping is the process of converting the virgin fibre into a form suitable for making paper and paperboard grades. In chemical pulping the fibres are broken down chemically: chemicals are used in a cooking process to enter the fibre lumen and dissolve lignin in the cell walls to gain access to the compound middle lamella (CML). Lignin has to be removed from the CML to free the fibres. The lignin and many other organic substances are thus put into solution. This happens in pressure vessels, called digesters, which in the case of batch processes are heated, pressurissed vertical stationary vessels for wood and often spherical ones arranged to rotate to unload the contents, for non-woods, or in the case of continuous processes are vertical tower constant flow digesters. Mechanical pulping processes use grinding for logs and disc refiners for chips. In these processes, mechanical shear forces are used to pull the fibres apart and the majority of the lignin remains with the fibres, although there is still some significant dissolution of organics. The first step is followed by secondary disc refining and direct supply to a paper machine. Mechanical pulps can often be used without bleaching, but where brightening is done it is achieved using non chlorinated compounds such as dithionite or peroxides. The main chemical semi-chemical and chemimechanical pulping techniques are: • • • • • • Lime, lime-soda especially non-wood fibres; Cold soda uses sodium hydroxide pre treatment at ambient temperatures, alone or with sodium carbonate; especially hardwood and non-wood fibres; (semi chemical). Soda AQ sodium hydroxide alone or with sodium carbonate and a catalyst anthraquinone, hardwood and non-wood fibres; (chemical, similar to kraft but without sulphur), reduced odour. Sulphate (kraft) uses a mixture of sodium hydroxide and sodium sulphide under alkaline conditions to dissolve the ligninfrom wood and most non-wood fibres; (chemical method). Sulphite - acid bisulphite, bisulphite, alkaline and neutral sulphite methods, (Ca, Mg, NH4, Na) different bases, including anthraquinone, under a range of pH, to dissolve the lignins, most wood fibres; (chemical and semichemical methods). Organosolv methods, wood and non-wood applications, some proven on mill scale: • Alcohol as a solvent (not in commercial use), organic acids as solvent; • Hybrid processes. The Kraft (Sulphate) Pulping Process 79 The kraft or sulphate process is an alkaline cooking liquor process and it is the dominating pulping process world wide (84 % of the world chemical pulp production and 63% of total chemical and mechanical pulp production). The kraft process uses a sodium based alkaline pulping solution consisting of sodium sulphide (Na2S) and sodium hydroxide (NaOH). Used cooking liquor (black liquor) is recovered to generate white liquor for the first pulping step. At mills with chemical recovery, most of the dissolved wood substances are combusted and the wastewater mainly contains the organics in condensates plus, at bleached mills, the substances dissolved during bleaching and the residues of the bleaching chemicals. Many small mills do not recover the liquor. The recovery of non-wood fibre liquors is problematic due to the high silica content of fibre materials, the rapid increase of the liquor viscosity during evaporation and difficulties in achieving high solids content in the concentrated liquor fed to the recovery system. However, this area of recovery technology is currently receiving much attention with some claims for viable processes. 80 Figure 1. Pulping process flows - kraft pulping example (EIPPCB BREF, 2001) Lime and Soda processes These are processes using simple alkaline cooking liquors in a similar process to kraft pulping but without the use of sulphur compounds. At mills with no chemical recovery, all the dissolved wood substances and pulping/bleaching chemicals remain in the wastewater apart from the volatiles incidentally released to atmosphere. The de-lignification ability is inadequate for low yield, high white, wood pulping. Its application to non-wood pulps is widespread and it is also used with oxygen for straw pulping. In the soda process, the chemistry is simplified as there is no added sulphur to form undesirable by-products and the hydroxide can be recovered by lime causticization of the sodium carbonate smelt. After cooking, pulps that are not to be bleached are refined to separate the fibres. Sulphite Pulping Processes 81 The sulphite pulping process is based on aqueous sulphur dioxide (SO2) and a base, calcium, sodium, magnesium or ammonium. This method is losing its importance and only 10% of the world pulp is produced by this method. Alkaline sulphite mills for non-wood fibres are often operated as a batch process and chemical recovery is generally not practised at such mills due to their small size and the complexity of chemical recovery from what is normally a sodium based process. Compared to kraft pulps sulphite pulps are relatively bright and are also relative easy to bleach with oxygen based chemicals such as peroxides. Bleaching The objective of bleaching is to further remove the small quantity of residual lignin left after cooking. All lignin cannot be removed selectively enough in a single bleaching stage, but pulp is usually bleached in three to five stages, using combinations of oxygen, hydrogen peroxide, ozone, peracetic acid, Caro’s acid, sodium hypochlorite, chlorine dioxide, chlorine and other chemicals or treatments. The first two stages primarily release and extracts lignin and the subsequent stages removes the lignin residues and finishes the product. These bleaching sequences are applied to maximise the bleaching effect of each component. Water is used to perform intermediate washes to remove extracted wastes from the pulp. Bleaching sequences where chlorine based chemicals are used are called Chlorine Chemical Bleaching (CCB). If molecular chlorine and hypochlorite are excluded, the abbreviation is Chlorine Dioxide Bleaching (CDB), or Elemental Chlorine Free Bleaching (ECF). If the sequence uses only oxygen based chemicals like oxygen, ozone, alkaline or acidic peroxide the term Oxygen Chemical Bleaching (OCB), or Totally Chlorine Free (TCF) can be used. ECF pulp bleached with chlorine dioxide accounts for the predominant share of roughly three-quarters of the bleached pulp produced worldwide. TCF pulp only accounts for about 6% and is primarily produced in mills in Northern and Central Europe. Roughly 20% of the bleached pulp produced world-wide is still bleached with some elemental chlorine. Hardwood and straw pulps are easier to bleach by non chlorine methods due to their lower lignin content to begin with and the bleaching effort required for sulphite pulps is less due to their higher pre bleach brightness. Bleaching with chlorine and hypohlorous acid Electrophilic bleaching chemical agents such as chlorine and hypochlorous acid may be used to achieve further delignification after pulping. These electrophilic bleaching agents react with all unsaturated structures, namely lignin structures, polysaccharide degradation products such as hexenuronic acid and extractive stuctures that contain carbon-carbon double bonds. These electrophilic bleaching agents are able to react with different unsubstituted aromatic carbon atoms in lignin to either: a) chlorinate (when the carbon is not bonded with an oxygen atom), b) chlorinate and depolymerize (via displacement of an α-hydroxyl group), or c) just depolymerize without chlorination (via hydroxylation) . 82 These chlorination or depolymerization reactions make lignin alkaline soluble and it can be removed from pulp in the alkaline bleaching stages of the bleaching sequence. The chlorination of non-aromatic structures, such as hexenuronic acid, does not lead to the formation of polychlorinated aromatic degradation products. Some examples of bleaching sequences when chlorine is used: CEH (non-woods) CEHD CEHDED (higher brightness) CEDED (CD)EDED With an oxygen de-lignification stage or reinforced extraction stage then: OCEH (non-woods) (D+C)(EO)D (non-woods) With oxygen de-lignification and reinforced extraction then: O(D+C)(EO)D (non-woods) O-(CD)EDED O-(CD)(EO)DED Bleaching sequence letters : C is elemental chlorine Cl2 E is alkaline extraction NaOH H is hypochlorite D is chlorine dioxide ClO2 (CD) is mixtures of chlorine and chlorine dioxide O is oxygen (EO) is alkaline extraction with oxygen Formation of 2378-TCDD/F Dioxins and furans (only 2378-TCDD and 2378-TCDF) may be formed in the bleaching process in which chlorine is used. Most of the formation of the 2378-TCDD and 2378-TCDF are generated in the C-stage via the reaction of chlorine with precursors of TCDD namely dibenzo-p-dioxin (DBD) and precursor of TCDF which is unchlorinated dibenzofuran (DBF). When these precursors are chlorinated, the key reaction is electrophilic aromatic substitution. The rate of this reaction will be dependent both on the concentration of the precursor and the concentration of chlorine. The levels of 2378-TCDD and 2378-TCDF are not determined by the content of the lignin in the pulp /R.M.Berry, B.I.Fleming et. al/ . The unchlorinated dioxin precursors are prevalent in certain mineral oils which are part of some defoamer formulations used in the pulp and paper industry and are the major source of precursors. Wood itself may be source of dioxin precursor. In particular compression wood contains higher concentrations of precursors than 83 normal wood. Compression of wood also contains higher levels of coumaryl-type lignin which may be a source of DBD- and DBF-like precursors. Elimination mechanisms for 2378-TCDD/F Preventing formation of 2378-TCDD and 2378-TCDF in the bleaching will be achieved mainly by decreasing the amount of chlorine used in the first bleaching stage. This can be done by reducing atomic chlorine multiple through use of oxygen and peroxide reinforced extraction stage and increased chlorine dioxide substitution. Figure 2. shows how formation 2378-TCDF will be reduced by increasing ClO2 substitution: when ClO2 substitution level is more than 85 % 2378-TCDF is not detectable in waste waters coming from the mill. 84 Figure 2. 2378-TCDF formation with different chlorine dioxide substitution level The summary effect of active chlorine multiple and chlorine dioxide substitution level can be see in the figure 3. The level of dioxin formation under these conditions, i.e., high active chlorine multiple and low chlorine dioxide substitution, is expected to vary depending on the DBD precursor content of the brownstock. 35 30 2,3,7,8 25 20 TCDD, 15 ppt 10 5 0 20 40 % ClO2 60 80 0.28 Substitution 100 0.20 0.24 0.16 0.12 Active chlorine multiple Figure 3. Effect of active chlorine multiple and chlorine dioxide substitution level on 2378-TCDD formation. 85 Elemental chlorine can completely be replaced by chlorine dioxide (Elemental Chlorine-Free bleaching ECF). In comparison withchlorine bleaching, ECF bleaching using chlorine dioxide leads to the formation of a relatively small amount of chlorinated compounds, but does not lead to the formation of 2378-TCDD/F. Chlorine is produced as a side product in some chlorine dioxide manufacturing methods, but in all cases this amount is too small for the unintentional production of 2378-TCDD/F. As a summary, the following measures can be made for eliminating or decreasing the formation of 2378-TCDD and 2378-TCDF: • • • Eliminate elemental chlorine via replacing with chlorine dioxide (ECF bleaching), or with chlorine free chemicals (TCF bleaching) Reduce application of elemental chlorine via decreasing chlorine multiple or increasing substitution of chlorine dioxide for molecular chlorine Minimize precursors like DBD and DBF entering the bleach plant by using precursor-free additives and good washing such Best Available Techniques (BAT) for production of pulp using elemental chlorine Primary measurements The principal Best Available Techniques to minimization or elimination of formation of 2378-TCDD/F are as follows and they are independent of the raw material (wood or non-wood) used in the process: • Eliminate molecular chlorine via replacing with chlorine dioxide (ECF bleaching), or with chlorine free chemicals (TCF bleaching) • Reduce application of molecular chlorine via decreasing chlorine multiple or increasing substitution of chlorine dioxide for molecular chlorine • • • Utilize DBD and DBF-free defoamers • • • Eliminate pulping of wood chips contaminated with polychlorinated phenol Effective brown stock washing to enable the reduction of chlorine multiple Maximize knot and dirt removal to enable the reduction of chlorine multiple Secondary measurements 86 The following general measures are suggested: • Substitution. The identification and substitution of potentially harmful substances with less harmful alternatives. Use of a detailed inventory of raw materials used, chemical composition, quantities, fate and environmental impact. • Investment planning/cycles, co-ordination of process improvements to reduce technical bottleneck delays to the introduction of better techniques. • Training, education and motivation of personnel. Training, education and motivation of staff and operators. People operate pulp and paper mills. Therefore, training of staff can be a very cost-effective way of reducing discharges of harmful substances. • Process control monitoring and optimisation. To be able to reduce different pollutants simultaneously and to maintain low releases, improved process control is required. Raw materials specification and monitoring of raw materials for precursor materials. • Adequate maintenance. To maintain the efficiency of the process and the associated abatement techniques at a high level, sufficient maintenance has to be ensured. • Environmental management system. A system which clearly defines the responsibilities for environmentally relevant aspects in a mill. It raises awareness and includes goals and measures, process and job instructions, check lists and other relevant documentation. Incorporation of environmental issues in process change controls. • Development of environmental monitoring and standard monitoring protocols. • Release monitoring for new facilities. Demonstrate performance of combustion processes and releases to water. Performance standards( Is this chapter necessary?) The following table summarises this information as it is applied to bleached kraft pulp mills: New Plant EU Canada - 2378-TCDD / 2378-TCDF ppq To Water 2378-TCDD / 2378-TCDF ng/kg To Sludge Non-measurable1 87 PCDD / PCDF ng/m3 STP TEQ To Air 0.1 0.1 Defoamers DBD and DBF ppb DBD <10 Federal – In treated final effluent USA Kraft and 2378-TCDD <10 10 / 100 Soda 2378-TCDF 31.9 In bleach plant effluent 2378-TCDD <10 USA 2378-TCDF <10 Ammonium -In bleach plant based and effluent speciality sulphite Australia 2378-TCDD <15 2378-TCDF none – In treated final effluent DBF <40 1. Non measurable - means a concentration less than the level of quantification as defined in the Reference Method. The current level of quantification is 15 ppq. Performance Reporting Performance reporting is recommended as follows: For dioxin and furan releases to water – a monthly testing period. A mill may adopt quarterly sampling if it has had no measurable concentrations in its last three consecutive monthly samples, a mill may adopt annual sampling if it has had no measurable concentrations in its last three consecutive quarterly samples. The testing period reverts back to monthly testing if either a quarterly test or an annual test exceeds the level of quantitation (LOQ). Treatment sludges used for agricultural benefit may also need to be tested before use. Where emissions testing is not possible (e.g., analytical capacity is not readily available), the use of PCDD/PCDF release factors associated with a similar mill type and operation is suggested as an interim performance reporting requirement until such time as annual emissions testing and analysis is available. Emission factors for releases of PCDD/PCDFs from mills are presented at page 184 in the UNEP Standardized Toolkit for Identification and Quantification of Dioxin and Furan Releases, May 2003 (URL:www.pops.int). The commonality of this issue across all sector guides would indicate that it needs to be covered as a separate report and draw on the information on performance levels and testing methods contained in each of the individual sector guides. 88 References: [AGIC, 1990] Australian Government, Industry Commission, Pulp and Paper: Bleaching and the Environment, Report no 1, May 1990, Australian Government Publishing Service Canberra, ISBN 0 644 12529 2. See http://www.pc.gov.au/ic/inquiry/01pulp/finalreport/01pulp.pdf [Pulp&paper Canada] R.M.Berry, B.I.Flemming, et. al. Toward preventing the formation of dioxins during chemical pulp bleaching. Pulp&Paper Canada, 90:8 1989. [CBNS, 1996] Pulp and Paper Production, Zeroing Out The Dioxin in the Great Lakes: Wthin Our Reach, Center for the Biology of Natural Systems (CBNS), Queens College, New York, June 1996. See http://www.cbns.qc.edu/cbns_ch5.pdf [CEPA Regulations (SOR/92-268), 1992] Canadian Pulp and Paper Mill Defoamer and Wood Chip Regulations (SOR/92-268), Canadian Department of Justice. See http://www.ec.gc.ca/NOPP/DIVISION/EN/detail.cfm?par_docID=99 [EA S6.01, 2000] IPPC S6.01 Integrated Pollution Prevention and Control (IPPC) Technical Guidance for the Pulp and Paper Sector, The Environment Agency for England and Wales, SEPA & EHS, Nov 2000. See http://environmentagency.gov.uk/business/444304/444635/107293/?version=1&lang=_e [EIPPCB BREF, 2001] Integrated Pollution Prevention and Control (IPPC) Reference Document on Best Available Techniques in Pulp and Paper Industry, European Commission, EIPPCB, December 2001. See: http://eippcb.jrc.es [Finnish BAT Report, 1997] The Finnish Background Report for the EC Documentation of Best Available Techniques for Pulp and Paper Industry. The Finnsih Environment 96, Ministry of Environment in Finland, Edita Ltd, Helsinki 1997, ISBN 952-11-0123-7 [PMS&T FAPET, Series, 1999] Johan Gullichsen and Hannu Paulapuro, Papermaking Science and Technology Series, 19 Volumes, FAPET Oy, Jyväskylä 1999. ISBN 952-5216-00-4 (Series). [PMS&T Vol 6, FAPET 1999] Johan Gullichsen and Carl-Johan Fogelholm, Chemical Pulping, Papermaking Science and Technology, Vols 6 A and B, FAPET Oy, Jyväskylä 1999. ISBN 952-5216-07-1. See http://fapet.fi [SEPA-Report 4713-2, 1997] Aspects on Energy and Environment Costs in Connection with Production of Kraft Pulp, Recycled Fibre and TMP. Jaakko Pöyry Consulting AB. 1997 [SYKE, No 17, 1996] J. Tana and K.J. Lehtinen: The Aquatic Environmental Impact of Pulping and Bleaching Operations – An Overview. Finnish Environment Agency (SYKE), 1996. ISBN 952-11-0028-1. [TAPPI, 1987] Pulp and Paper Manufacture Volume 3, Secondary Fibers and NonWood Pulping, F. Hamilton, B. Leopold and M.J. Kocurek, TAPPI, 1987. 89 [TU Darmstadt, 2002] U. Hamm and L. Göttsching: Comparison of the aquatic environmental impact resulting from the production of ECF and TCF sulphate pulp, Concise assessment of current knowledge VDP – INFOR project (No. 19), Institut für Papierfabrikation, TU Darmstadt (Institute for Papermaking, Darmstadt Technical University), December 2002. [USC, 1989] U.S Congress, Office of Technology Assessment, Technologies for Reducing Dioxin in the Manufacture of Bleached Wood Pulp, OTA-BP-O-54 (Washington, DC: U.S. Government Printing Office, May 1989). See: http://govinfo.library.unt.edu/ota/Ota_2/DATA/1989/8931.PDF [USEPA, 2003] Effluent Guidelines – Final Pulp and Paper Cluster Rule, Federal Register: April 15, 1998 (Volume 63, Number 72), USEPA. See: http://www.epa.gov/waterscience/pulppaper/cluster.html [VTT Biotechnology, 2003] VTT Biotechnology, Marcus Wallenberg Prize 2003, See http://www.mwp.org and http://vtt.fi [World Bank, 1998] World Bank Pollution Prevention and Abatement Handbook 1998 – Toward Cleaner Production. See http://wwwwds.worldbank.org/servlet/WDS_IBank_Servlet?pcont=details&eid=000094946_990 40905052283 90 DEFINITIONS ADt & ODt Air dried tonne of paper (paper contains around 7% water under ambient conditions). ODt oven dried. AOX Adsorbable Organic Halogen APP Alkaline peroxide process BAT Best Available Techniques Bleaching Sequence letters : C is elemental chlorine Cl2 E is alkaline extraction NaOH H is hypochlorite D is chlorine dioxide ClO2 (CD) is mixtures of chlorine and chlorine dioxide O is oxygen (EO) is alkaline extraction with oxygen P is hydrogen peroxide (EOP) is alkaline extraction with oxygen and hydrogen peroxide aP is hydrogen peroxide in acidic conditions (PO) is peroxide pressurised with oxygen (DN) is chlorine dioxide with subsequent neutralisation Z is ozone Paa is peracetic acid Ca is Caro’s acid (sulphuric acid and hydrogen peroxide) Pxa is mixed peracids Q is chelation stage X is enzyme treatment BOD Biochemical Oxygen Demand COD Chemical Oxygen Demand CTMP Chemi-thermo-mechanical-pulping processes (using sulphite or APP) DAF Dissolved air flotation DBD Dibenzodioxin DBF Dibenzofuran DTPA Diethylene triamino pentaacetic acid ECF Elemental chlorine free (pulp bleached without elemental chlorine) EDTA Ethylene diamine tetra-acetic acid EMS Environmental Management System Kappa No The Kappa number is an indirect measure of the residual lignin content in a pulp measured via the consumption of an oxidant chemical (e.g. potassium permanganate). Measure used for process control. Integrated-mill A mill in which both pulping and papermaking take place I-TEQ International Toxicity Equivalents or TEQ (Toxic Equivalents) I-TEF International Toxicity Equivalency Factor or TEF (Toxicity Equivalence Factor) NTA Nitrilo triacetic acid PAE Polyamidoamine-epichlorhydrin resins PAM Polyacrylamides PCDDs Polychlorinated dibenzo-para-dioxins PCDFs Polychlorinated dibenzofurans PCP Pentachlorophenol PCB Polychlorinated biphenyls PEI Polyethyleneimines 91 RCF Recycled fibre TCDD 2,3,7,8 –tetrachloro-para-dibenzodioxin TCDF 2,3,7,8 – tetrachloro dibenzofuran TCF Totally chlorine free (pulp bleached without any chlorine compounds) TOC Total Organic Carbon Wood-free Paper made from pulp from which the lignin has been largely dissolved by chemical mean 92 COMMENTS SUBMITTED BY GAIA: GLOBAL ALLIANCE FOR INCINERATION ALTERNATIVES 93 94 95 96 97 98 99 COMMENTS SUBMITTED BY GREENPEACE INTERNATIONAL greenpeace international Ottho Heldringstraat 5, 1066 AZ, Amsterdam, Netherlands t +31 514 8150 f +31 20 514 8151 k.v.k. reg. 41200415 stichting greenpeace council www.greenpeace.org 16 June 2004 Comments on draft guidelines on best available techniques and guidance on best environmental practices relevant to Article 5 and Annex C of the Stockholm Convention on Persistent Organic Pollutants By Pat Costner Senior Science Advisor Greenpeace International We appreciate this opportunity to comment on the latest draft guidelines and guidance. It was agreed at EGB-2 that a section on alternatives would included in the draft guideline/guidance document. Reflecting that agreement, “Consideration of Alternatives” is listed as the second chapter in the table of contents of this document. It was also agreed to include similar, appropriately specific alternatives chapters in each of the guidance/guidelines for individual source categories. However, as is evident, all of the latter documents do not include an alternatives chapter and, consequently, require revision to correct this oversight. Below are brief comments, both specific and general, on the guidelines/guidance document as a whole as well as on guidance/guidelines for several of the individual source categories. Chapter/Section Comment 1.A. Purpose Despite its title, there is no mention in this segment of the actual purpose of the guidelines and guidance. • The purpose of the guidelines and guidance can be broadly described as providing Parties with information that will help them to achieve the goal of the Stockholm Convention with respect to unintentionally produced POPs (UPOPs) – the “continuing minimization and, where feasible, ultimate elimination” of UPOPs. • The purpose of the guidelines and guidance can be described more specifically as providing Parties with information that will help them to meet their obligations to promote and in some cases require the use of best available techniques (BAT) and to promote the use of BEP in order to achieve the goal of the Stockholm Convention with respect to UPOPs – the “continuing minimization and, where feasible, ultimate elimination” of UPOPs. We suggest that this segment is revised so that it begins with one or both of the above statements, or reasonably similar text. 100 II. Consideration The title of this section –“Consideration of alternatives” as it is listed of alternatives in the table of contents – is so vague that many readers are likely to skip past it and go directly to the apparent “meat” of the document, “V. Guidance/guidelines by source category: Annex C, Part II Source Categories,” and “VI. Guidance/guidelines by source category: Annex C, Part III Source Categories.” A more meaningful title – “Consideration of alternative processes, activities and chemicals” – can be taken from the text of the Convention, e.g., in the preamble – “Recognizing the importance of developing and using environmentally sound alternative processes and chemicals” -- and in Annex C, Part V.A – “When considering proposals to construct new waste disposal facilities, consideration should be given to alternatives such as activities to minimize the generation of municipal and medical waste, including resource recovery, reuse, recycling, waste separation and promoting products that generate less waste.” With several types of suggested text distinguished by color, this section is difficult to read and the meaning of the text is hard to discern. However, the general approach -- a “checklist” methodology -- has considerable merit and should be retained. In addition, this section requires substantial revision if it is to serve as the overarching discussion of alternatives to be included in this guidance/guideline as agreed at EGB-2. V.A. Waste incinerators: 1. Municipal and hazardous waste and sewage sludge This draft guidance/guideline includes a large mass of information. However, a significant share of that information is repetitive. For example, flue gas treatment is addressed in great detail both in section 4.0 and yet again in sub-section 6.2. At the same time, important information is lacking. For example, while the widespread use of waste incinerators in developed nations as well as some developing nations is noted, there is no accompanying description of the contribution of waste incinerators to UPOPs releases to air, water, land, products and residues in some of these same countries, although such data are readily available. Similarly, there is no mention of the relatively numerous studies and reviews that have examined the association between impacts on public health and the environment and waste incinerators. While the details of incinerator designs can be appreciated, the size of this document could be markedly reduced, its organization improved and its contents simplified by referring readers who desire a high level of detail to the EU BREF. In addition to the agreement at EGB-2 to include an overarching discussion of alternatives, it was also agreed to include guidance on alternatives in the guideline/guidance for each source category. Following the model of the overall guideline/guidance document, based on its table of contents, the alternatives sub-section of this guideline/guidance for waste incinerators should follow the introduction or, as it is called here, “1.0 Background.” 101 However, as this guideline/guidance is currently organized, the one section that might be construed as addressing alternatives occurs near the end of the report. It is listed in the table of contents as “9.0 Alternative and Emerging Technologies” and titled in the text as “9.0 Emerging Technologies.” The information in this sub-section consists only of brief discussions of pyrolysis and gasification, thermal depolymerization, plasma technologies, and high temperature melting. Some of these are considered to be incineration technologies by some authorities, such as the European Commission, and all are potential sources of UPOPs. The purpose of this guidance/guideline is described in “1.0 Background” as follows: The environmentally sound design and operation of waste incinerators requires the use of best environmental practices and best available techniques to prevent or minimize the formation and release of the unintentional POPs. The purpose of this guidance is to identify such practices and techniques, summarize their effectiveness, and estimate their relative cost, for consideration by the Parties in the development of national action plans under the Stockholm Convention on Persistent Organic Pollutants”. We suggest revising the above purpose so that it is compatible with the obligations defined by the Convention with respect to UPOPs and UPOPs sources. For example, the Convention clearly recognizes that “alternatives such as activities to minimize the generation of municipal and medical waste, including resource recovery, reuse, recycling, waste separation and promoting products that generate less waste, including resource recovery, reuse, recycling, waste separation and promoting products that generate less waste” (see Annex C, Part V.A) as BAT/BEP for UPOPs sources including waste incinerators. It is interesting to note that this guidance states that “poorly designed or operated incinerators can lead to the unintentional formation and release of persistent organic pollutants (dioxins and furans [PCDD/F], and unintentionally produced polychlorinated biphenyls [PCBs] and hexachlorobenzene [HCB].” There is no argument that UPOPs formation and releases may be much higher with poorly designed and operated incinerators. However, the formation and release of UPOPs from even the most modern, well-designed and operated waste incinerators is welldocumented. Similarly inaccurate statements are made with respect to hazardous waste incinerators and sewage sludge incinerators. The notion of folding together of BAT/BEP for municipal waste incinerators, hazardous waste incinerators and sewage sludge incinerators can be seen to have merit in that it potentially avoids the repetition of certain types of information, such as flue gas cleaning techniques. However, in this document, it has also created a circumstance in which the section on BEP for waste incineration offers information on waste minimization for municipal waste only. Since this guidance/guidelines is intended for use by Parties that are developing countries, the information presented that can be expected to be relevant predominantly to industrialized countries should be clearly 102 identified. For example, the contents of municipal wastes differ greatly, depending on levels of development, as indicated by gross national product. For example, in developing countries, municipal waste commonly has a higher moisture content and higher levels of inert materials such as dirt and sand so that volume and weight reductions achieved by incineration may be considerably less, the mass of bottom ash may be larger, energy recovery may be considerably reduced, etc. Such factors should be presented and discussed in this guidance/guideline. Many developing countries have no hazardous waste or lined, monitored landfills for the disposal of incinerator ash and no municipal wastewater treatment systems that can appropriately treat incinerator scrubber water. The economic implications of such factors should also be addressed in this document. It is also interesting to note that there is no mention of chlorine in Section “2.0 Formation and Release of Unintentional POPs,” while it is mentioned in Section “3.2.1 Delivery, Storage and Pre-Treatment of MSW” --“Recycling paper, cardboard, and plastics will reduce the energy value of the waste but may also reduce available chlorine” – with no explanation of why reducing available chlorine is relevant to UPOPs formation and release. We suggest revising Section 2.0 so that the role of chlorine in UPOPs formation is explained. Toward that end, we offer the following explanation of PCDD/F formation which can be suitably simplified: The prerequisites for PCDD/F formation in thermal processes are the following: • • • • Chlorine in the form of gaseous, elemental chlorine; as organic chlorine, such as chlorobenzene, polyvinyl chloride (PVC), etc.; or as inorganic chloride, such as hydrogen chloride, sodium chloride (table salt), etc.; Carbon in the form of macromolecular carbon in fly ash, soot , and/or the activated carbon that is used to reduce releases in flue gases, or in the form of organically-bound carbon in compounds that have escaped combustion or formed as products of incomplete combustion; Oxygen as gaseous, elemental oxygen or as oxygen in organic or inorganic forms e.g., PCDD/PCDF formation can take place in a nitrogen atmospherei; and Hydrogen in any form.. PCDD/PCDF formation in thermal processes is thought to occur primarily through these pathways: 1. High-temperature, gas-phase formation in homogeneous12 reactions of chlorine, either in elemental form or as hydrogen chloride, and gaseous precursors13; 12 In this context, the term “homogeneous’ means that all reactants are in the same physical state (gaseous, liquid or solid), while in “heterogeneous” reactions, reactants differ in their physical states. 103 2. Relatively low-temperature formation from the reaction of macromolecular14 carbon, which occurs in fly ash, soot and activated carbon, with organic or inorganic chlorine present in the fly ash, (often referred to as de novo formation); and 3. Formation in heterogeneous reactions of gas-phase organic precursors with metal oxides, metal chlorides or other catalytically active constituents on fly ash, other particulates or solid surfaces. . The relative importance of these pathways varies, depending on conditions. However, the two latter pathways are thought to be most important in modern, well-operated incinerators. Conditions that favour PCDD/PCDF formation in thermal processes are as follows: • • VI.A Open burning of wastes Elevated temperatures: Formation of PCDD/PCDF in the combustion zones of lab- and full-scale combustion systems has been reported to occur in the range of 500-1000 oC . ii, iii, iv Formation in post-combustion zones, including air pollution control devices, of full-scale incinerators via de novo synthesis or another heterogeneous pathway has been found to occur at temperatures as low as 150 oC. v However, the optimum temperature for PCDD/PCDF formation in the post-combustion zone has been reported to range between 650 and 250 °C, with maximum formation at approximately 300 °C. vi Metals (for example, copper and iron, vii zinc,viii and manganeseix) can serve as catalysts that increase and expedite PCDD/PCDF formation. However, some studies have shown that metals may not be required.x . In “1.1 General Process Consideration”, we suggest the following revised text: In the short term, where there are no realistic alternatives to open burning, practical techniques that are likely to reduce UPOPs generation include: • Reduce as much as possible the amount of material burned, O Remove non-combustibles such as glass and bulk metals O Remove other materials of low fuel value; O Remove wet materials; 13 A precursor is a substance from which another substance is formed, for example, chlorobenzenes and chlorophenols are precursors of PCDD/PCDF formation in combustion processes. A precursor is commonly regarded as being somewhat similar in chemical structure to the substance for which it is a precursor. 14 Macromolecular carbon is carbon that possesses a structure in which all of the carbons are linked by chemical bonds. 104 • • • • O Remove chlorine-containing materials such as PVC, salty food scraps, etc.; O Remove metal-containing materials such as scrap wire, cans, etc. Supply sufficient air, e.g., do not compact wastes; Burn in piles rather than confined spaces such as barrels; Maintain a steady rate of combustion; and Minimize smoldering by, if needed, extinguishing the fire. We note that there are numerous studies, including open burning of various materials, that have found increased chlorine content in the materials burned to correlate with increased PCDD/PCDF formation. An annotated bibliography of such studies has been prepared by Costner (2001).xi In section 3.1.2, we suggest deletion of the following sentence: “The preferred combustion alternative is BAT incineration with energy recovery, however combustors run the gamut from BAT incineration through a continuum of decreasing technology and efficiency to open pile or pit or “barrel” burning.” In section 3.2.1 Material Composition, we suggest including PVC among the materials in “Construction waste” as well as “Demolition waste.’ In section 3.1.3 Strategies and Policy Instruments to Avoid, Reduce or Divert Waste, we suggest including policies that reduce and/or change the character of consumer products and materials that, upon becoming wastes, contribute to the formation and release of UPOPs when subjected to open burning. Such products and materials include those that are made of or contain chlorinated materials, such as PVC plastic. In section 3.2.3 Strategies and Policy Instruments to Avoid, Reduce or Divert Waste, we suggest including policies that reduce and/or change the character of construction products and materials that, upon becoming wastes, contribute to the formation and release of UPOPs when subjected to open burning. Such products and materials include those that are made of or contain chlorinated materials, such as PVC siding, PVC pipe, etc. In section 4.1.3 Strategies and Policy Instruments to Avoid, Reduce or Divert Waste, we suggest including policies that reduce and/or change the character of agricultural film which, upon becoming a waste, contributes to the formation and release of UPOPs when subjected to open burning. Such agricultural films include those that are made of or contain chlorinated materials, such as PVC plastic. In section 4.2.4 Alternatives, Barriers to Use and Policy Instruments to Remove Barriers, we suggest including the following in the text: Dedicated tire incinerators have been identified as UPOPs sources,xii while co-combustion tires and coal is associated with increased 105 PAH emissions.xiii VI.F. Chemical production processes We suggest that the following is included as the introductory section of this document; The World Chlorine Council describes chemical production processes in which formation of PCDD/PCDF occurs as follows:xiv “Dioxins can be formed in chemical processes, where the element chlorine is involved.” The other basic prerequisites for PCDD/PCDF formation in industrialchemical processes are the presence of carbon, oxygen and hydrogen. For example, PCDD/PCDF formation takes place during the manufacture of elemental chlorine when graphite electrodes are used, as is commonly the case in China.xv USEPA (1997) described the factors that influence PCDD/PCDF formation in the manufacture of organic chemicals as follows: xvi “A number of factors influence the amount of dioxins and furans that may be formed in a given manufacturing process, including temperature, pH, catalyst, and reaction kinetics. … Four major mechanisms have been postulated for the formation of halogenated dioxins and furans in the manufacture of halogenated organic chemicals: (1) direct halogenation of dioxins or furans …); (2) reaction of an ortho halogen with a phenate…; (3) loss of the halogen (e.g., chlorine or bromine) from a halogenated phenate to form halogenated furans … ; and (4) reactions between ortho- and meta-substituted halogens ….” With regard to PCDD/PCDF formation in the manufacture of organic chemicals, Fiedler et al. (2000) noted as follows: xvii “In wet-chemical processes the propensity to generate PCDD/PCDF during synthesis of chemical compounds decreases in the following order: Chlorophenols < Chlorobenzenes < Aliphatic chlorinated compounds < Inorganic chlorinated compounds” i Wikstrom, E., Tysklind, M., Marklund, S., 1999. Influence of variation of combustion conditions on the primary formation of chlorinated organic micropollutants during municipal solid waste combustion. Environ. Sci. Technol. 33: 4263-4269. 106 ii Wikstrom, E., Tysklind, M., Marklund, S., 1999. Influence of variation of combustion conditions on the primary formation of chlorinated organic micropollutants during municipal solid waste combustion. Environ. Sci. Technol. 33: 4263-4269. iii Zimmermann, R., Blumenstock, M., Heger, H., Schramm, K.-W., Kettrup, A., 2001. Emission of nonchlorinated and chlorinated aromatics in the flue gas of incineration plants during and after transient disturbances of combustion conditions: Delayed emission effects. Environ. Sci. Technol. 35: 1019-1030. iv Stanmore, B., 2004. The formation of dioxins in combustion systems. Combustion & Flame 136: 398-427. v Chang, M., Lin, J., 2001. Memory effect on the dioxin emissions from municipal waste incinerator in Taiwan. Chemosphere 45: 1151-1157 vi Tuppurainen, K., Halonen, I., Rukokojarvi, P., Tarhanen, J., Ruuskanen, J., 1998. Formation of PCDDs and PCDFs in municipal waste incineration and its inhibition mechanisms: A review. Chemosphere 36: 1493-1511. vii Ryan, S., Altwicker, E., 2004. Understanding the role of iron chlorides in the de novo synthesis of polychlorinated dibenzo-p- dioxins/dibenzofurans. Environ. Sci. Technol. 38: 1708-1717 viii Hinton W.S., Lane A.M., Synthesis of polychlorinated dioxins over MSW incinerator fly ash to identify catalytic species. Chemosphere, 23, 831-840, 1991. ix Halonen, I., Tarhanen, J., Ruokojarvi, P., Tuppurainen, K., Ruuskanen, J., 1995. Effect of catalysts and chlorine source on the formation of organic chlorinated compounds. Chemosphere 30: 1261-1273. x Sidhu, S., Kasti, N., Edwards, P., Dellinger, B., 2001. Hazardous air pollutants formation from reactions of raw meal organics in cement kilns. Chemosphere 42: 499-506. xi Costner, P., 2001. Chlorine, Combustion and Dioxins: Does Reducing Chlorine in Wastes Decrease Dioxin Formation in Waste Incinerators? Amsterdam, Netherlands: Greenpeace International. xii U.S. Environmental Protection Agency, 2000. Exposure and Human Health Reassessment of 2,3,7,8Tetrachlorodibenzo-p-Dioxin (TCDD) and Related Compounds. Part I: Estimating Exposure to Dioxin-Like Compounds. Volume 2: Sources of Dioxin-Like Compounds in the United States, EPA/600/P-00/001Bb, Draft Final Report, September 2000. www.epa.gov/ncea xiii Levendis, Y., Atal, A., Carlson, J. 1998. On the Correlation of CO and PAH Emissions from the Combustion of Pulverized Coal and Waste Tires Environ. Sci. Technol. 32: 3767-3777 xiv World Chlorine Council, 1998. Dioxins and Furans in the Chemical Industry. http://www.eurochlor.org/chlorine/issues/dioxins.htm (Accessed 16 March 2004). xv Xu, Y., Zhang, Q., Wu, W., Li, W., 2000. Patterns and levels of PCDD/F in a Chinese graphite electrode sludge. Chinese Science Bulletin 45: 1471- 1475. xvi U.S. Environmental Protection Agency, 1997. Locating and Estimating Air Emissions from Sources of Dioxins and Furans. EPA 454/R-97-003. Research Triangle Park, NC: U.S. Environmental Protection Agency. xvii Fiedler, H., Hutzinger, O., Welsch-Pausch, K., Schmiedinger, A., 2000. Evaluation of the Occurrence of PCDD/PCDF and POPs in Wastes and Their Potential to Enter the Foodchain. Final Report. Study on behalf of the European Commission, DG Environment. Bayreuth, Germany: University of Bayreuth. 107
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