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Effect of selected additions on de novo synthesis of polychlorinated dioxins and furans Cover

Effect of selected additions on de novo synthesis of polychlorinated dioxins and furans

Open Access
|Jul 2016

References

  1. [1] Poland A, Knutson JC. 2,3,7,8-tetrachlorodibeno-p-dioxin and related halogenated aromatic hydrocarbons. Examination of the mechanism of toxicity. Annual Rev Pharmacol Toxicol. 1982;22:517-554. DOI: 10.1146/annurev.pa.22.040182.002505.10.1146/annurev.pa.22.040182.002505
  2. [2] Boening DW. Toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin to several ecological receptor groups: a short review. Ecol Environ Safety. 1998;39:155-163. DOI: 10.1006/eesa.1997.1608.10.1006/eesa.1997.1608
  3. [3] Cole P, Trichopoulos D, Pastides H, Starr T, Mandel JS. Dioxin and cancer: a critical review. Regulatory Toxicol Pharmacol. 2003;38(3):378-388. DOI: 10.1016/j.yrtph.2003.08.002.10.1016/j.yrtph.2003.08.002
  4. [4] Wielgosiński G. Emisja dioksyn z procesów termicznych i metody jej ograniczania (Dioxin emissions from thermal processes and methods of emission reduction). Łódź: Polska Akademia Nauk (Polish Academy of Sciences); 2009.
  5. [5] Rappe C. Sources of exposure, environmental concentrations and exposure assessment of PCDDs and PCDFs. Chemosphere. 1993;27:211-225. DOI: 10.1016/0045-6535(93)90295-G.10.1016/0045-6535(93)90295-G
  6. [6] Bumb RR., Crummett WB, Artie SS, Gledhill JR, Hummel RH, Kagel RO, et al. Trace chemistries of fire: a source of chlorinated dioxins. Science. 1980;210:385-390. DOI: 10.1126/science.6159682.10.1126/science.6159682
  7. [7] Ballschmiter K, Zoller W, Buchert H, Clas Th. Correlation between substitution pattern and reaction pathway in the formation of polychlorodibenzofurans. Fresenius Zeit Analit Chem. 1985;322:587-594. DOI: 10.1007/BF00464594.10.1007/BF00464594
  8. [8] Dickson LC, Karasek FW. Model studies of polychlorinated dibenzo-p-dioxin formation during municipal refuse incineration. Science. 1987;237:754-756. DOI: 10.1126/science.3616606.10.1126/science.3616606
  9. [9] Vogg H, Stieglitz L. Thermal behavior of PCDD/PCDF in fly ash form municipal incinerators. Chemosphere. 1986;15:1373-1378. DOI: 10.1016/0045-6535(86)90412-1.10.1016/0045-6535(86)90412-1
  10. [10] Wielgosinski G. The possibilities of reduction of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans emission. Int J Chem Eng. 2010; Article ID 392175. DOI: 10.1155/2010/392175.10.1155/2010/392175
  11. [11] McKay G. Dioxin characterization, formation and minimization during municipal solid waste (MSW) incineration. A Review. Chem Eng J. 2002;86:343-368. DOI: 10.1016/S1385-8947(01)00228-5.10.1016/S1385-8947(01)00228-5
  12. [12] Ruokojärvi P, Asikainen A, Tuppurainen K, Ruuskanen J. Chemical inhibition of PCDD/F formation in incineration processes. Sci Total Environ. 2004;325:83-94. DOI: 10.1016/j.scitotenv.2003.11.006.10.1016/j.scitotenv.2003.11.00615144780
  13. [13] Boscolo M, Padoano E, Tommasi S. Identification of possible dioxin emission reduction strategies in pre-existing iron ore sinter plants. Ironmaking Steelmaking. 2008;35:146-152. DOI: 10.1179/174328107X247815.10.1179/174328107X247815
  14. [14] Öberg T, Bergbäck B, Filipsson M. Catalytic effect by metal oxides on the formation and degradation of chlorinated aromatic compounds in fly ash. Chemosphere. 2008;71:135-1143. DOI: 10.1016/j.chemosphere.2007.10.033.10.1016/j.chemosphere.2007.10.03318061236
  15. [15] Ke S, Jianhua Y, Xiaodong L, Shengyong L, Yinglei W, Muxing F. Inhibition of de novo synthesis of PCDD/Fs by SO2 in a model system. Chemosphere. 2010;78:1230-1235. DOI: 10.1016/j.chemosphere.2009.12.043.10.1016/j.chemosphere.2009.12.04320074772
  16. [16] Chen T, Zhan M, Lin X, Li X, Lu S, Yan J, et al. Inhibition of the de novo synthesis of PCDD/Fs on model fly ash by sludge drying gases. Chemosphere. 2014;114:226-232. DOI: 10.1016/j.chemosphere.2014.03.123.10.1016/j.chemosphere.2014.03.12325113206
  17. [17] Fu JY, Li XD, Chen T, Lin XQ, Buekens A, Lu SY, et al. PCDD/Fs’ suppression by sulfur-amine/ammonium compounds. Chemosphere. 2015;123:9-16; DOI: 10.1016/j.chemosphere.2014.10.073.10.1016/j.chemosphere.2014.10.07325481352
  18. [18] Takaoka M, Fujimori T, Shiono A, Yamamoto T, Takeda N, Oshita K, et al. Formation of chlorinated aromatics in model fly ashes using various copper compounds. Chemosphere. 2010;80:144-149. DOI: 10.1016/j.chemosphere.2010.04.005.10.1016/j.chemosphere.2010.04.00520452643
DOI: https://doi.org/10.1515/eces-2016-0017 | Journal eISSN: 2084-4549 | Journal ISSN: 1898-6196
Language: English
Page range: 249 - 257
Published on: Jul 7, 2016
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2016 Grzegorz Wielgosiński, Olga Namiecińska, Patrycja Łechtańska, Adam Grochowalski, published by Society of Ecological Chemistry and Engineering
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.