Dioxin characterisation, formation and minimisation during municipal solid waste (MSW) incineration: review

被引:693
作者
McKay, G [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem Engn, Kowloon, Hong Kong, Peoples R China
关键词
municipal solid waste incineration; polychlorinated dibenzodioxins; polychlorinated dibenzofurans;
D O I
10.1016/S1385-8947(01)00228-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The present review discusses the current views on methods to minimise dioxins, namely polychlorinated dibenzodioxins (PCDDs) and dibenzofurans (PCDFs), formation in MSW incineration systems. The structure of this group of compounds is discussed initially and then the toxic equivalence scale is presented for the most common isomers and congeners in the dioxin family. The current status on dioxin limits imposed in various countries and by various organisations is presented. A detailed analysis of the theories leading to dioxin formation in MSW incineration is given, since, this has been one of the most controversial areas of dioxin chemistry for the past 20 years. Three dioxin formation theories were considered possible for a long timed (i) from PCDD/PCDFs originally present in the furnace feedstock; (ii) from precursor compounds (foundation formatting molecules which could react rapidly with other groups in the system to form dioxins) in the MSW feed; (iii) from de novo synthesis of smaller, relatively innocuous chemical molecules combining together to form the dioxins. Methods (ii) and (iii) are based on heterogeneously catalysed reactions. Some researchers are considering possible homogeneous thermal reaction formation of dioxin. This review demonstrates that with the advanced modem MSW combustion systems, option (i) is a most unlikely route and also methods (ii) and (iii) are quite feasible. Based on thermodynamic and kinetic data in the literature, the rate and extent of the formation of dioxins and their precursors by certain mechanisms can definitely be contributing to routes (ii) and (iii). Since even the most advanced MSW combustion systems do not produce complete combustion, predominantly because of inadequate feed preparation and turbulence, some de novo synthesis of precursors can also take place. These 'de novo precursors' could be carried through the combustion unit adsorbed or absorbed on particulate material such as soot and dust, but also these precursors could be formed during the cooling process by heterogeneous catalytic reactions and go on to form dioxins. The maximum rate of formation of PCDD/PCDFs from both sources lies in the temperature range 300-400 degreesC. This knowledge of formation rates and mechanisms provides the basis of designing combustion systems. A two stage approach is adopted firstly, system design to achieve complete combustion and minimise formation; secondly, end-of-pipe treatment systems to remove dioxins. In the first case, combustion temperature should be above 1000 degreesC, combustion residence time should be greater than 1 s, combustion chamber turbulence should be represented by a Reynolds number greater than 50,000, good MSW feed preparation and controlled feed rate are also critical. In the second category, very rapid gas cooling from 400 to 250 degreesC should be achieved, semi-dry lime scrubbing and bag filtration coupled with activated carbon injection adsorption as end-of-pipe treatments can all play a role in prevention or minimisation of dioxins in the final flue gas emission to the atmosphere, (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:343 / 368
页数:26
相关论文
共 220 条
[1]   Isomer distributions of polychlorinated dibenzo-p-dioxins/dibenzofurans formed during de novo synthesis on incinerator fly ash [J].
Addink, R ;
Govers, HAJ ;
Olie, K .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (13) :1888-1893
[2]   FORMATION OF POLYCHLORINATED DIBENZO-PARA-DIOXINS DIBENZOFURANS IN THE CARBON FLY-ASH SYSTEM [J].
ADDINK, R ;
DRIJVER, DJ ;
OLIE, K .
CHEMOSPHERE, 1991, 23 (8-10) :1205-1211
[3]   MECHANISMS OF FORMATION AND DESTRUCTION OF POLYCHLORINATED DIBENZO-P-DIOXINS AND DIBENZOFURANS IN HETEROGENEOUS SYSTEMS [J].
ADDINK, R ;
OLIE, K .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (06) :1425-1435
[4]   INFLUENCE OF HCL AND CL-2 ON THE FORMATION OF POLYCHLORINATED DIBENZO-P-DIOXINS/DIBENZOFURANS IN A CARBON/FLY ASH MIXTURE [J].
ADDINK, R ;
BAKKER, WCM ;
OLIE, K .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (08) :2055-2058
[5]   REDUCTIVE DECHLORINATION OF PCDD/F BY ANAEROBIC CULTURES AND SEDIMENTS [J].
ADRIAENS, P ;
GRBICGALIC, D .
CHEMOSPHERE, 1994, 29 (9-11) :2253-2259
[6]   IMPACT OF POLYCHLORINATED DIBENZO-P-DIOXINS, DIBENZOFURANS, AND BIPHENYLS ON HUMAN AND ENVIRONMENTAL-HEALTH, WITH SPECIAL EMPHASIS ON APPLICATION OF THE TOXIC EQUIVALENCY FACTOR CONCEPT [J].
AHLBORG, UG ;
BROUWER, A ;
FINGERHUT, MA ;
JACOBSON, JL ;
JACOBSON, SW ;
KENNEDY, SW ;
KETTRUP, AAF ;
KOEMAN, JH ;
POIGER, H ;
RAPPE, C ;
SAFE, SH ;
SEEGAL, RF ;
TUOMISTO, J ;
VANDENBERG, M .
EUROPEAN JOURNAL OF PHARMACOLOGY-ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY SECTION, 1992, 228 (04) :179-199
[7]   Comparative study on formations of polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans and related compounds in a fluidized bed solid waste incinerator using long term used sand and fresh sand [J].
Akimoto, Y ;
Nito, S ;
Inouye, Y .
CHEMOSPHERE, 1997, 34 (04) :791-799
[8]   Improvements to the UK PCDD/F and PCB atmospheric emission inventory following an emissions measurement programme [J].
Alcock, RE ;
Gemmill, R ;
Jones, KC .
CHEMOSPHERE, 1999, 38 (04) :759-770
[9]   Dioxin-like PCBs in the environment - Human exposure and the significance of sources [J].
Alcock, RE ;
Behnisch, PA ;
Jones, KC ;
Hagenmaier, H .
CHEMOSPHERE, 1998, 37 (08) :1457-1472
[10]   FORMATION OF DIOXINS - COMPETING RATES BETWEEN CHEMICALLY SIMILAR PRECURSORS AND DE-NOVO REACTIONS [J].
ALTWICKER, ER ;
MILLIGAN, MS .
CHEMOSPHERE, 1993, 27 (1-3) :301-307