In the study the most important and known polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzo-furans (PCDFs) emission sources are presented and known methods of reduction of dioxin emission to the atmosphere are discussed in detail. It is indicated that the most relevant emission source is a combustion process. The mechanism of dioxin formation in thermal processes is presented in brief. The author characterized primary methods of reduction of PCDDs/PCDFs emission encompassing the interference into the combustion process to minimize their formation and discussed known secondary methods aimed at their removal from the stream of waste gases. It was attempted to make a critical assessment of PCDD/Fs reduction methods described in literature. 1. Introduction On 23 May, 2001 in Stockholm there was signed the Convention concerning persistent organic pollutants (POPs). The reason for the convention was the necessity to regulate the issues connected with the production and utilization of certain organic substances—the so-called persistent organic pollutants. The convention introduced relevant limitations in the production, application, export, and import of POPs, as well as strict requirements concerning the record and monitoring. One of the most important decisions of Convention was the commitment to the continuous minimization or the final elimination of the release of such substances as dioxins and furan (PCDD/Fs), hexachlorobenzene (HCB) (as a precursor of dioxin synthesis) as well as polychlorinated biphenyls (PCBs)—as compounds with similar toxicity to dioxins, to the environment This indicates the necessity of the implementation of the best available techniques (BAT) to the industrial practice in the following fields: waste incineration, paper-mills using chlorine for whitening, steel mills and copper, aluminum and zinc mills, refineries utilizing waste oils, crematories, power plants, and thermal-electric power plants as well as the other activities. Polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans are categorized as the so-called endocrine disrupters—the substances disturbing the activity of the endocrine system. Since 1970s PCDD/Fs have been thought to belong to the group of the strongest poisons among the known chemical compounds so far. Nevertheless, in spite of very high toxicity of certain dioxins and furans with regard to some animal organisms, one may find it difficult to compare PCDD/Fs with the other strong toxins present in the environment. This is because their activity is not instantaneous in the
References
[1]
A. Poland and J. C. Knutson, “2,3,7,8-tetrachlorodibenzo-p-dioxin and related halogenated aromatic hydrocarbons: examination of the mechanism of toxicity,” Annual Review of Pharmacology and Toxicology, vol. 22, pp. 517–554, 1982.
[2]
D. W. Boening, “Toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin to several ecological receptor groups: a short review,” Ecotoxicology and Environmental Safety, vol. 39, no. 3, pp. 155–163, 1998.
[3]
M. Kogevinas, “Human health effects of dioxins: cancer, reproductive and endocrine system effects,” Human Reproduction Update, vol. 7, no. 3, pp. 331–339, 2001.
[4]
A. J. J. Mendes, “The endocrine disrupters: a major medical challenge,” Food and Chemical Toxicology, vol. 40, no. 6, pp. 781–788, 2002.
[5]
P. Cole, D. Trichopoulos, H. Pastides, T. Starr, and J. S. Mandel, “Dioxin and cancer: a critical review,” Regulatory Toxicology and Pharmacology, vol. 38, no. 3, pp. 378–388, 2003.
[6]
P. Boffetta, “Human cancer from environmental pollutants: the epidemiological evidence,” MMutation Research/Genetic Toxicology and Environmental Mutagenesis, vol. 608, no. 2, pp. 157–162, 2006.
[7]
“The European Dioxin Emission Inventory. Stage II,” European Commission DG ENV, Bruxelles, Belgium, 2000.
[8]
G. Thanner and W. Moche, Emission von Dioxinen, PCBs und PAHs aus Kleinfeuerungen, vol. 153 of Monographien, Umweltbundesamt, Wien, Austria, 2002.
[9]
W. V. Ligon Jr., S. B. Dorn, R. J. May, and M. J. Allison, “Chlorodibenzofuran and chlorodibenzo-p-dioxin levels in Chilean mummies dated to about 2800 years before the present,” Environmental Science and Technology, vol. 23, no. 10, pp. 1286–1290, 1989.
[10]
R. E. Alcock and K. C. Jones, “Dioxins in the environment: a review of trend data,” Environmental Science and Technology, vol. 30, no. 11, pp. 3133–3143, 1996.
[11]
R. E. Alcock, M. S. Mclachlan, A. E. Johnston, and K. C. Jones, “Evidence for the presence of PCDD/Fs in the environment prior to 1900 and further studies on their temporal trends,” Environmental Science and Technology, vol. 32, no. 11, pp. 1580–1587, 1998.
[12]
K. Olie, P. L. Vermeulen, and O. Hutzinger, “Chlorodibenzo-p-dioxins and chlorodibenzofurans are trace components of fly ash and flue gas of some municipal incinerators in the Netherlands,” Chemosphere, vol. 6, no. 8, pp. 455–459, 1977.
[13]
H. R. Buser, H.-P. Bosshardt, and C. Rappe, “Identification of polychlorinated dibenzo-p-dioxin isomers found in fly ash,” Chemosphere, vol. 7, no. 2, pp. 165–172, 1978.
[14]
R. R. Bumb, W. B. Crummett, and S. S. Cutie, “Trace chemistries of fire: a source of chlorinated dioxins,” Science, vol. 210, no. 4468, pp. 385–390, 1980.
[15]
C. Rappe, “Sources of PCDDs and PCDFs. Introduction. Reactions, levels, patterns, profiles and trends,” Chemosphere, vol. 25, no. 1-2, pp. 41–44, 1992.
[16]
J. I. Baker and R. A. Hites, “Is combustion the major source of polychlorinated dibenzo-p-dioxins and dibenzofurans to the environment? A mass balance investigation,” Environmental Science and Technology, vol. 34, no. 14, pp. 2879–2886, 2000.
[17]
G. Wielgosiński, Dioxins Emission from Thermal Processes, PAN, ?ód?, Poland, 2009.
[18]
W. B. Crummett and D. I. Townsend, “The trace chemistries of fire hypothesis: review and update,” Chemosphere, vol. 13, no. 7, pp. 777–788, 1984.
[19]
H. Hunsinger, K. Jay, and J. Vehlow, “Formation and destruction of PCDD/F inside a grate furnace,” The Chemosphere, vol. 46, no. 9-10, pp. 1263–1272, 2002.
[20]
K. Ballschmiter, W. Zoller, H. Buchert, and T. H. Clas, “Correlation between substitution pattern and reaction pathway in the formation of polychlorodibenzofurans,” Fresenius' Zeitschrift für Analytische Chemie, vol. 322, no. 6, pp. 587–594, 1985.
[21]
H. Vogg and L. Stieglitz, “Thermal behavior of PCDD/PCDF in fly ash from municipal incinerators,” Chemosphere, vol. 15, no. 9–12, pp. 1373–1378, 1986.
[22]
F. W. Karasek and L. C. Dickson, “Model studies of polychlorinated dibenzo-p-dioxin formation during municipal refuse incineration,” Science, vol. 237, no. 4816, pp. 754–756, 1987.
[23]
H. Huang and A. Buekens, “On the mechanisms of dioxin formation in combustion processes,” Chemosphere, vol. 31, no. 9, pp. 4099–4117, 1995.
[24]
K. Ballschmiter and M. Swerev, “Reaction pathways for the formation of polychlorodibenzodioxins (PCDD) and -furans (PCDF) in combustion processes I,” Fresenius' Zeitschrift für Analytische Chemie, vol. 328, no. 1-2, pp. 125–127, 1987.
[25]
K. Ballschmiter, I. Braunmiller, R. Niemczyk, and M. Swerev, “Reaction pathways for the formation of polychloro-dibenzodioxins (PCDD) and dibenzofurans (PCDF) in combustion processes: II. Chlorobenzenes and chlorophenols as precursors in the formation of poly-chloro-dibenzodioxins and dibenzofurans in flame chemistry,” Chemosphere, vol. 17, no. 5, pp. 995–1005, 1988.
[26]
W. A. Rubey, B. Dellinger, D. L. Hall, and S. L. Mazer, “High-temperature gas-phase formation and destruction of polychlorinated dibenzofurans,” Chemosphere, vol. 14, no. 10, pp. 1483–1494, 1985.
[27]
C. M. Young and K. J. Voorhees, “PIC formation mechanisms in the thermal decomposition of 1,2-dichlorobenzene,” Chemosphere, vol. 23, no. 8–10, pp. 1265–1277, 1991.
[28]
G. H. Eduljee, “Organic micropollutant emissions from waste incineration,” in Waste Incineration and the Environment, R. E. Hester and R. M. Harrison, Eds., Royal Society of Chemistry, Cambridge, UK, 1994.
[29]
K. Jay and L. Stieglitz, “Identification and quantification of volatile organic components in emissions of waste incineration plants,” Chemosphere, vol. 30, no. 7, pp. 1249–1260, 1995.
[30]
A. Trenholm, “Identification of PICs in hazardous waste combustion emissions,” Waste Management, vol. 18, no. 6–8, pp. 485–492, 1998.
[31]
J. Wienecke, H. Kruse, U. Huckfeldt, W. Eickhoff, and O. Wassermann, “Organic compounds in the flue gas of a hazardous waste incinerator,” Chemosphere, vol. 30, no. 5, pp. 907–913, 1995.
[32]
E. R. Altwicker, R. K. N. V. Konduri, C. Lin, and M. S. Milligan, “Formation of precursors to chlorinated dioxin/furans under heterogeneous conditions,” Combustion Science and Technology, vol. 88, no. 5-6, pp. 349–368, 1993.
[33]
L. C. Dickson, D. Lenoir, and O. Hutzinger, “Surface-catalyzed formation of chlorinated dibenzodioxins and dibenzofurans during incineration,” Chemosphere, vol. 19, no. 1–6, pp. 277–282, 1989.
[34]
L. Stieglitz and H. Vogg, “On formation conditions of PCDD/PCDF in fly ash from municipal waste incinerators,” Chemosphere, vol. 16, no. 8-9, pp. 1917–1922, 1987.
[35]
L. Stieglitz, G. Zwick, J. Beck, W. Roth, and H. Vogg, “On the de-novo synthesis of PCDD/PCDF on fly ash of municipal waste incinerators,” Chemosphere, vol. 18, no. 1–6, pp. 1219–1226, 1989.
[36]
R. D. Griffin, “A new theory of dioxin formation in municipal sold waste combustion,” Chemosphere, vol. 15, no. 9–12, pp. 1987–1990, 1986.
[37]
B. K. Gullett, K. R. Bruce, L. O. Beach, and A. M. Drago, “Mechanistic steps in the production of PCDD and PCDF during waste combustion,” Chemosphere, vol. 25, no. 7–10, pp. 1387–1392, 1992.
[38]
T. ?berg, B. Bergb?ck, and M. Filipsson, “Catalytic effects by metal oxides on the formation and degradation of chlorinated aromatic compounds in fly ash,” Chemosphere, vol. 71, no. 6, pp. 1135–1143, 2008.
[39]
L. C. Dickson, D. Lenoir, and O. Hutzinger, “Quantitative comparison of de novo and precursor formation of polychlorinated dibenzo-p-dioxins under simulated municipal solid waste incinerator postcombustion conditions,” Environmental Science and Technology, vol. 26, no. 9, pp. 1822–1828, 1992.
[40]
T. D. Goldfarb, “Evidence for post-furnace formation of PCDDs and PCDFs—implications for control,” Chemosphere, vol. 18, no. 1–6, pp. 1051–1055, 1989.
[41]
G. Wielgosiński, “Emissions from waste incineration plants—primary methods of emission reduction,” Energetic Policy, vol. 6, pp. 131–140, 2003.
[42]
B. Gullett and R. Seeker, “Chlorinated dioxin and furan control and monitoring,” in Proceedings of the Interfaith Center on Corporate Responsibility (ICCR '97), Research Triangle Park, 1997.
[43]
R. Ishikawa, A. Buekens, H. Huang, and K. Watanabe, “Influence of combustion conditions on dioxin in an industrial-scale fluidized-bed incinerator: experimental study and statistical modelling,” Chemosphere, vol. 35, no. 3, pp. 465–477, 1997.
[44]
K. Watanabe and K. Tsukamoto, “Emission control of dioxin compounds in plastic waste incineration,” Organohalogen Compounds, vol. 19, pp. 431–434, 1994.
[45]
G. Schmoekel and A. Streit, Emissionen Organischer Stoffe Bei Der Holzfeuerung Wackersdorf, Bayerisches Landesamt ftir Umweltschutz, Augsburg College, Minneapolis, MN, USA, 1994.
[46]
R. Seeker, “Current understanding of dioxin/furan formation and control,” private communication.
[47]
R. L. Lindbauer, F. Wurst, and T. Prey, “Combustion dioxin suppression in municipal solid waste incineration with sulphur additives,” Chemosphere, vol. 25, no. 7–10, pp. 1409–1414, 1992.
[48]
B. K. Gullett, K. R. Bruce, and L. O. Beach, “Effect of sulfur dioxide on the formation mechanism of polychlorinated dibenzodioxin and dibenzofuran in municipal waste combustors,” Environmental Science Technology, vol. 26, no. 10, pp. 1938–1943, 1992.
[49]
H. Huang and A. Buekens, “De novo synthesis of polychlorinated dibenzo-p-dioxins and dibenzofurans. Proposal of a mechanistic scheme,” The Science of the Total Environment, vol. 193, no. 2, pp. 121–141, 1996.
[50]
P. H. Ruokoj?rvi, I. A. Halonen, K. A. Tuppurainen, J. Tarhanen, and J. Ruuskanen, “Effect of gaseous inhibitors on PCDD/F formation,” Environmental Science and Technology, vol. 32, no. 20, pp. 3099–3103, 1998.
[51]
C. Xhrouet and E. de Pauw, “Prevention of dioxins de novo synthesis by ethanolamines,” Environment Chemistry Letters, vol. 1, pp. 51–56, 2003.
[52]
P. H. Ruokoj?rvi, A. H. Asikainen, K. A. Tuppurainen, and J. Ruuskanen, “Chemical inhibition of PCDD/F formation in incineration processes,” Science of the Total Environment, vol. 325, no. 1–3, pp. 83–94, 2004.
[53]
S. Kuzuhara, H. Sato, N. Tsubouchi, Y. Ohtsuka, and E. Kasai, “Effect of nitrogen-containing compounds on polychlorinated dibenzo-p-dioxin/dibenzofuran formation through de novo synthesis,” Environmental Science and Technology, vol. 39, no. 3, pp. 795–799, 2005.
[54]
M. E. Pandelova, D. Lenoir, A. Kettrup, and K.-W. Schramm, “Primary measures for reduction of PCDD/F in co-combustion of lignite coal and waste: effect of various inhibitors,” Environmental Science and Technology, vol. 39, no. 9, pp. 3345–3350, 2005.
[55]
J. J. Cudahy and R. W. Helsel, “Removal of products of incomplete combustion with carbon,” Waste Management, vol. 20, no. 5-6, pp. 339–345, 2000.
[56]
H. J. Fell and M. Tuczek, “Removal of dioxins and furans from flue gases by non-flammable adsorbents in a fixed bed,” Chemosphere, vol. 37, no. 9–12, pp. 2327–2334, 1998.
[57]
J. Blumbach and L. P. Nethe, “PCDD/F/PCB reduction in flue gases and residual materials from waste incineration by use of carbonaceous adsorbents,” Organohalogen Compounds, vol. 19, pp. 305–310, 1994.
[58]
S. Okajima, T. Kojima, S. Ueoka, and H. Ozaki, “Fixed-bed adsorption of polychlorinated dibenzo-p-dioxins and dibenzofurans from flue gas a municipal solid waste incinerator,” Organohalogen Compounds, vol. 54, pp. 193–196, 2001.
[59]
R. Maierhofer and H. Grochowski, “Removal of dioxins and furans with activated carbon countercurrent flow process,” Organohalogen Compounds, no. 19, pp. 361–364, 1994.
[60]
K. Everaert, J. Baeyens, and C. Creemers, “Adsorption of dioxins and furans from flue gases in an entrained flow or fixed/moving bed reactor,” Journal of Chemical Technology and Biotechnology, vol. 78, no. 2-3, pp. 213–219, 2003.
[61]
K. Everaert and J. Baeyens, “Removal of PCDD/F from flue gases in fixed or moving bed adsorbers,” Waste Management, vol. 24, no. 1, pp. 37–42, 2004.
[62]
K. Mori, H. Matsui, N. Yamaguchi, and Y. Nakagawa, “Multi-component behavior of fixed-bed adsorption of dioxins by activated carbon fiber,” Chemosphere, vol. 61, no. 7, pp. 941–946, 2005.
[63]
M. Yates, J. Blanco, P. Avila, and M. P. Martin, “Honeycomb monoliths of activated carbons for effluent gas purification,” Microporous and Mesoporous Materials, vol. 37, no. 1-2, pp. 201–208, 2000.
[64]
M. Reinmark, D. van der Kleut, and B. van der Akker, “Norit powdered activated carbon in flue gas clean up,” Organohalogen Compounds, vol. 27, pp. 177–182, 1996.
[65]
H. Hagenmeier, “Katalytische oxidation halogenierter kohlenwasserstoffe unter besonderer berücksichtigung des dioxinproblems,” VDI Berichte, vol. 730, pp. 239–254, 1989.
[66]
M. Hiraoka, N. Takeda, S. Okajima, T. Kasakura, and Y. Imoto, “Catalytic destruction of PCDDs in flue gas,” Chemosphere, vol. 19, no. 1–6, pp. 361–366, 1989.
[67]
H. Hagenmaier and G. Mittelbach, “Versuche zum Katalytischen NOx und Dioxin Abbau im Abgas einer Hausmüllverbrennungsanlage,” VGB-Kraftwerkstechnik, vol. 70, no. 6, pp. 491–493, 1990.
[68]
H. von Fahlenkamp, G. Mittlebach, H. Hagenmeier, H. Brunner, and K.-H. Tichaczek, “Katalytische Oxidation. Eine Technik zur Verminderung der PCDD-/PCDF-Emission aus Müllverbrennungsanlagen auf kleiner 0,1?ng TE/ ,” VGB kraftwerkstechnik, vol. 71, no. 7, pp. 671–674, 1991.
[69]
R. Boos, R. Budin, H. Hartl, M. Stock, and F. Wurst, “PCDD- and PCDF- destruction by a SCR-unit in a municipal waste incinerator,” Chemosphere, vol. 25, no. 3, pp. 375–382, 1992.
[70]
Y. Ide, K. Kashiwabara, S. Okada, T. Mori, and M. Hara, “Catalytic decomposition of dioxin from MSW incinerator flue gas,” Chemosphere, vol. 32, no. 1, pp. 189–198, 1996.
[71]
P. Andersson, C. Rappe, O. Maaskant, J. F. Unsworth, and S. Marklund, “Low temperature catalytic destruction of PCDD/F in flue gas from waste incineration,” Organohalogen Compounds, vol. 36, pp. 109–248, 1998.
[72]
W. Schüttenhelm, R. Wemh?ner, H. U. Hartenstein, and K. Werner, “Reduction of PCDD/F emission from iron ore sintering plants—the first full-scale SCR installation,” Organohalogen Compounds, vol. 40, pp. 453–456, 1999.
[73]
R. Weber, T. Sakurai, and H. Hagenmaier, “Low temperature decomposition of PCDD/PCDF, chlorobenzenes and PAHs by -based - catalysts,” Applied Catalysis B, vol. 20, no. 4, pp. 249–256, 1999.
[74]
H. C. Choi, C. G. Park, H. J. Seung, and Oh T. Y., “Catalytic destruction of PCDDs/DFs by the SCR units,” Organohalogen Compounds, vol. 45, pp. 387–391, 2000.
[75]
C. C. Hyun, G. P. Cheon, J. S. Hee, and T. Y. Oh, “Catalytic destruction of PCDDs/DFs by SCR units,” Organohalogen Compounds, vol. 45, pp. 387–390, 2000.
[76]
M. Goemans, P. Clarysse, J. Joannès et al., “Catalytic NOx reduction with simultaneous dioxin and furan oxidation,” Chemosphere, vol. 54, no. 9, pp. 1357–1365, 2004.
[77]
F. Bertinchamps, Total oxidation of chlorinated VOCs on supported oxide catalysts, Ph.D. thesis, Universite Catholique de Louvain, Louvain, Belgium, 2005.
[78]
G. Wielgosiński, A. Grochowalski, T. Machej, T. Paj?k, and W. ?wi?kalski, “Catalytic destruction of dioxins on - / - catalyst effect of temperature and catalyst loading,” Organohalogen Compounds, vol. 60, pp. 2242–2245, 2005.
[79]
E. Finocchio, G. Busca, and M. Notaro, “A review of catalytic processes for the destruction of PCDD and PCDF from waste gases,” Applied Catalysis B, vol. 62, no. 1-2, pp. 12–20, 2006.
[80]
V. de Jong, M. K. Cieplik, and R. Louw, “Formation of dioxins in the catalytic combustion of chlorobenzene and a micropollutant-like mixture on Pt/γ- ,” Environmental Science and Technology, vol. 38, no. 19, pp. 5217–5223, 2004.
[81]
R. W. van den Brink, R. Louw, and P. Mulder, “Formation of polychlorinated benzenes during the catalytic combustion of chlorobenzene using a Pt/γ- catalyst,” Applied Catalysis B, vol. 16, no. 3, pp. 219–226, 1998.
[82]
J. R. Hart, “Verification of dioxin formation in a catalytic oxidizer,” Chemosphere, vol. 72, no. 1, pp. 75–78, 2008.
[83]
G. Wielgosiński, A. Grochowalski, T. Machej, and W. ?wi?kalski, “Dioxin Formation over Pt/Pd catalyst,” in Proceedings of the 29th International Symposium on Halogenated Persistent Ogranic Pollutants (DIOXIN '09), Beijing, China, August 2009.
[84]
M. Plinke, K. Fritsky, C. P. Gantara, et al., “Catalytic dioxin/furan removal from flue gas streams,” Organohalogen Compounds, vol. 45, pp. 452–455, 2000.
[85]
R. Weber, M. Plinke, and Z. Xu, “Dioxin destruction efficiency of catalytic filters—evaluation in laboratory and comparison to field operation,” Organohalogen Compounds, vol. 45, pp. 427–430, 2000.
[86]
K. J. Fritsky, J. H. Kumm, and M. Wilken, “Combined PCDD/F destruction and particulate control in a baghouse: experience with a catalytic filter system at a medical waste incineration plant,” Journal of the Air and Waste Management Association, vol. 51, no. 12, pp. 1642–1649, 2001.
[87]
G. Pranghofer, “Destruction of polychlorinated dibenzo-p-dioxins and dibenzofurans in fabric filters: recent experiences with a catalytic filter system,” in Proceedings of the 3rd International Symposium on Incineration and Flue Gas Treatment Technologies (INCINERATION '01), Brussels, Belgium, June 2001.
[88]
J. L. Bonte, M. Plinke, R. Dandaraw, et al., “Catalytic filtration: dioxin/furan destruction in the baghouse. Experiences at the IVRO municipal waste incinerator in Roeselare,” Organohalogen Compounds, vol. 40, pp. 459–464, 1999.
[89]
J. L. Bonte, K. J. Fritsky, M. A. Plinke, and M. Wilken, “Catalytic destruction of PCDD/F in a fabric filter: experience at a municipal waste incinerator in Belgium,” Waste Management, vol. 22, no. 4, pp. 421–426, 2002.
[90]
M. Syc, V. Pekarek, E. Fioserova, M. Puncochar, J. Karban, and O. Kokes, “Catalytic filter application in the termizo municipal waste incineration plant in Liberec,” Organohalogen Compounds, vol. 68, pp. 1232–1235, 2006.
[91]
S. Kreisz, H. Hunsinger, and H. Vogg, “Technical plastics as PCDD/F absorbers,” Chemosphere, vol. 34, no. 5–7, pp. 1045–1052, 1997.
[92]
S. Kreisz, H. Hunsinger, and H. Seifert, “Polypropylene as regenerable absorber for PCDD/F emission control,” Chemosphere, vol. 40, no. 9–11, pp. 1029–1031, 2000.
[93]
S. Kreisz, H. Hunsinger, and H. Seifert, “Carbon doped propylene as PCDD/F adsorber,” Organohalogen Compounds, vol. 56, pp. 369–372, 2002.
[94]
S. Andersson, S. Kreisz, and H. Hunsinger, “PCDD/F removal from flue gases in wet scrubbers—a novel technique,” Organohalogen Compounds, vol. 58, pp. 157–160, 2002.
[95]
S. Andersson, S. Kreisz, and H. Hunsinger, “Innovative material technology removes dioxins from flue gases,” Filtration and Separation, vol. 40, no. 10, pp. 22–25, 2003.
[96]
S. Andersson, S. Kreisz, and H. Hunsinger, “PCDD/F removal from flue gases using Adiox,” Organohalogen Compounds, vol. 63, pp. 244–247, 2003.
[97]
S. Andersson, “PCDD/F removal from gases using a dry adiox absorber,” Organohalogen Compounds, vol. 67, pp. 2226–2229, 2005.
[98]
S. Andersson, S. Kreisz, and H. Hunsinger, “Dioxin removal: ADIOX for wet scrubbers and dry absorbers,” Filtration and Separation, vol. 42, no. 12, pp. 22–25, 2005.
[99]
H.-R. Paur, W. Baumann, H. M?tzing, and K. Jay, “Electron beam induced decomposition of chlorinated aromatic compounds in waste incinerator offgas,” Radiation Physics and Chemistry, vol. 52, no. 1–6, pp. 355–359, 1998.
[100]
G. Y. A. Gerasimov, “Simulation of the nehavior of dioxins under the conditions of electron-beam gas cleaning of sulfur and nitrogen oxides,” High Energy Chemistry, vol. 37, no. 3, pp. 141–145, 2003.
[101]
H. Nichipor, E. Dashouk, S. Yacko, A. G. Chmielewski, Z. Zimek, and Y. Sun, “Chlorinated hydrocarbons and PAH decomposition in dry and humid air by electron beam irradiation,” Radiation Physics and Chemistry, vol. 65, no. 4-5, pp. 423–427, 2002.
[102]
K. Hirota, T. Hakoda, M. Taguchi, M. Takigami, H. Kim, and T. Kojima, “Application of electron beam for the reduction of PCDD/F emission from municipal solid waste incinerators,” Environmental Science and Technology, vol. 37, no. 14, pp. 3164–3170, 2003.
[103]
A. G. Chmielewski, Y.-X. Sun, S. Bulka, and Z. Zimek, “Chlorinated aliphatic and aromatic VOC decomposition in air mixture by using electron beam irradiation,” Radiation Physics and Chemistry, vol. 71, no. 1-2, pp. 435–438, 2004.
[104]
A. G. Chmielewski, Y. Sun, S. Bu?ka, and Z. Zimek, “Review on gaseous chlorinated organics pollutants electron beam treatment,” Radiation Physics and Chemistry, vol. 76, pp. 1795–1801, 2007.
[105]
K. Hirota and T. Kojima, “Decomposition behavior of PCDD/F isomers in incinerator gases under electron-beam irradiation,” Bulletin of the Chemical Society of Japan, vol. 78, no. 9, pp. 1685–1690, 2005.
[106]
H. Y. Jian, P. Zheng, Y. L. Sheng, et al., “Destruction of PCDD/Fs formed by pentachlorophenol via gliding arc discharges,” Organohalogen Compounds, vol. 68, pp. 1247–1250, 2006.
[107]
M. Nifuku, M. Horváth, J. Bodnár et al., “A study on the decomposition of volatile organic compounds by pulse corona,” Journal of Electrostatics, vol. 40-41, pp. 687–692, 1997.
[108]
D. Crespo and R. T. Yang, “Adsorption of organic vapors on single-walled carbon nanotubes,” Industrial and Engineering Chemistry Research, vol. 45, no. 16, pp. 5524–5530, 2006.
[109]
S. B. Fagan, E. J. G. Santos, A. G. Souza Filho, J. Mendes Filho, and A. Fazzio, “Ab initio study of 2,3,7,8-tetrachlorinated dibenzo-p-dioxin adsorption on single wall carbon nanotubes,” Chemical Physics Letters, vol. 437, no. 1–3, pp. 79–82, 2007.
[110]
R. T. Yang, R. Q. Long, J. Padin, A. Takahashi, and T. Takahashi, “Adsorbents for dioxins: a new technique for sorbent screening for low-volatile organics,” Industrial and Engineering Chemistry Research, vol. 38, no. 7, pp. 2726–2731, 1999.
[111]
R. Q. Long and R. T. Yang, “Carbon nanotubes as superior sorbent for dioxin removal,” Journal of the American Chemical Society, vol. 123, no. 9, pp. 2058–2059, 2001.
[112]
Y.-H. Shih and M.-S. Li, “Adsorption of selected volatile organic vapors on multiwall carbon nanotubes,” Journal of Hazardous Materials, vol. 154, no. 1–3, pp. 21–28, 2008.
[113]
J. Choi, O. Kim, and S.-Y. Kwak, “Suppression of dioxin emission in co-incineration of poly(vinyl chloride) with -encapsulating polystyrene,” Environmental Science and Technology, vol. 41, no. 16, pp. 5833–5838, 2007.
[114]
J. L. Graham, C. B. Almquist, S. Kumar, and S. Sidhu, “An investigation of nanostructured vanadia/titania catalysts for the oxidation of monochlorobenzene,” Catalysis Today, vol. 88, no. 1-2, pp. 73–82, 2003.
[115]
Y. Jiamg, S. Decker, C. Mohs, and K. J. Klabunde, “Catalytic solid state reactions on the surface of nanoscale metal oxide particles,” Journal of Catalysis, vol. 180, no. 1, pp. 24–35, 1998.
[116]
S. H. Kim, S.-Y. Ahn, and S.-Y. Kwak, “Suppression of dioxin emission in incineration of poly(vinyl chloride) (PVC) as hybridized with titanium dioxide nanoparticles,” Applied Catalysis B, vol. 79, no. 3, pp. 296–305, 2008.
[117]
P. S. Kulkarni, L. C. Branco, J. G. Crespo, and C. A. M. Afonso, “Capture of dioxins by ionic liquids,” Environmental Science and Technology, vol. 42, no. 7, pp. 2570–2574, 2008.
[118]
G. Fernández-Martínez, P. López-Mahía, S. Muniategui-Lorenzo, D. Prada-Rodríguez, and E. Fernández-Fernández, “Distribution of volatile organic compounds during the combustion process in coal-fired power stations,” Atmospheric Environment, vol. 35, no. 33, pp. 5823–5831, 2001.
[119]
G. Fernández-Martínez, J. M. López-Vilari?o, P. López-Mahía et al., “First assessment of dioxin emissions from coal-fired power stations in Spain,” Chemosphere, vol. 57, no. 1, pp. 67–71, 2004.
[120]
C.-M. Chen, “The emission inventory of PCDD/PCDF in Taiwan,” Chemosphere, vol. 54, no. 10, pp. 1413–1420, 2004.
[121]
L.-F. Lin, W.-J. Lee, H.-W. Li, M.-S. Wang, and G.-P. Chang-Chien, “Characterization and inventory of PCDD/F emissions from coal-fired power plants and other sources in Taiwan,” Chemosphere, vol. 68, no. 9, pp. 1642–1649, 2007.
[122]
D. Herrmann and R. Herzschuh, “Formation of PCDD/F during thermal treatment of lignite,” Journal of Analytical and Applied Pyrolysis, vol. 49, no. 1, pp. 211–220, 1999.
[123]
O. Schleicher, A. Jensen, T. Herrmann, O. Roots, and A. Tordik, “Dioxin emission from two oil shale fired power plants in Estonia,” Organohalogen Compounds, vol. 66, pp. 1635–1641, 2004.
[124]
A. Grochowalski and J. Konieczyński, “PCDDs/PCDFs, dl-PCBs and HCB in the flue gas from coal fired CFB boilers,” Chemosphere, vol. 73, no. 1, pp. 97–103, 2008.
[125]
E. Aries, D. R. Anderson, N. Ordsmith, K. Hall, and R. Fisher, “Development and validation of a method for analysis of " dioxin-like" PCBs in environmental samples from the steel industry,” Chemosphere, vol. 54, no. 1, pp. 23–31, 2004.
[126]
L.-C. Wang, W.-J. Lee, P.-J. Tsai, W.-S. Lee, and G.-P. Chang-Chien, “Emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans from stack flue gases of sinter plants,” Chemosphere, vol. 50, no. 9, pp. 1123–1129, 2003.
[127]
H. C. Kai, H. C. Shu, and B. C. Moo, “PCDD/F emissions and distributions in Waelz plant and ambient air during different operating stages,” Environmental Science and Technology, vol. 41, no. 7, pp. 2515–2522, 2007.
[128]
H.-W. Li, W.-J. Lee, K.-L. Huang, and G.-P. Chang-Chien, “Effect of raw materials on emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans from the stack flue gases of secondary aluminum smelters,” Journal of Hazardous Materials, vol. 147, no. 3, pp. 776–784, 2007.
[129]
T. ?berg, “Low-temperature formation and degradation of chlorinated benzenes, PCDD and PCDF in dust from steel production,” The Science of the Total Environment, vol. 382, no. 1, pp. 153–158, 2007.
[130]
European Parliament and the Council Directive 2000/76/EC of 4 December 2000 on the incineration of waste. - OJ No L 196, p. 1, 2000/12/10.