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Warianty tytułu
Języki publikacji
Abstrakty
The focus of this study is to investigate the applicability of natural mineral iron disulfide (pyrite) in degradation of aromatic compounds including benzene and several chlorinated benzenes (from mono-chlorinated benzene (CB), di-chlorinated benzenes (di-CBs) to tri-chlorobenzenes (tri-CBs) in aerobic pyrite suspension by using laboratory batch experiments at 25°C and room pressure. At first, chlorobenzene was studied as a model compound for all considered aromatic compounds. CB was degraded in aerobic pyrite suspension, transformed to several organic acids and finally to CO2 and Clˉ. Transformations of remaining aromatic compounds were pursued by measuring their degradation rates and CO2 and Clˉ released with time. Transformation kinetics was fitted to the pseudo-first-order reactions to calculate degradation rate constant of each compound. Degradation rates of the aromatic compounds were different depending on their chemical structures, specifically the number and position of chlorine substituents on the benzene ring in this study. Compounds with the highest number of chlorine substituent at m-positions have highest degradation rate (1,3,5-triCB > 1,3-diCB > others). Three chlorine substituents closed together (1,2,3-triCB) generated steric hindrance effects. Therefore 1,2,3-triCB was the least degraded compound The degradation rates of all compounds were in the following order: 1,3,5-triCB > 1,3-diCB > 1,2,4-triCB ≅1,2-diCB ≅CB ≅benzene > 1,4-diCB > 1,2,3-triCB. The final products of the transformations were CO2 and Clˉ. Oxygen was the common oxidant for pyrite and aromatic compounds. The presence of aromatic compounds reduced the oxidation rate of pyrite, which reduced the amount of ferrous and sulfate ions release to aqueous solution.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
115--125
Opis fizyczny
Bibliogr. 33 poz., fot., schem., tab., wykr.
Twórcy
autor
- International University, Vietnam National University – Ho Chi Minh City
autor
- Tohoku University
Bibliografia
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- 6. Bruice, P.Y. (2004). Organic chemistry. Prentice Hall, NJ, USA. Carlson, D.L., McGuire, M.M., Roberts, A.L. & Fairbrother, D.H. (2003). Influence of surface composition on the kinetics of alachlor reduction by iron pyrite, Environmental Science & Technology, 37(11), pp. 2394-2399.
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- 14. Hao, J., Cleveland, C., Lim, E., Strongin, D.R. & Schoonen, M.A. (2006). The effect of adsorbed lipid on pyrite oxidation under biotic conditions, Geochemical Transactions, 7(1), 8.
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- 22. Nesbitt, H.W., Scaini, M., Hochst, H., Bancroft, G.M., Schaufuss, A.G. & Szargan, R. (2000). Synchrotron XPS evidence for Fe2+-S and Fe3+-S surface species on pyrite fracture-surfaces, and their 3D electronic states, American Mineralogist, 85(5-6), pp. 850-857.
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- 30. Weerasooriya, R. & Dharmasena, B. (2001). Pyrite-assisted degradation of trichloroethene (TCE), Chemosphere, 42(4), pp. 389-396.
- 31. Xu, X., Zhou, M., He, P. & Hao, Z. (2005). Catalytic reduction of chlorinated and recalcitrant compounds in contaminated water, Journal of Hazardous Materials, 123(1-3), pp. 89-93.
- 32. Zhang, L., Sawell, S., Moralejo, C. & Anderson, W.A. (2007). Heterogeneous photocatalytic decomposition of gas-phase chlorobenzene, Applied Catalysis B: Environmental, 71(3-4), pp. 135-142.
- 33. Zhu, B. W., Lim, T.T. & Feng, J. (2006). Reductive dechlorination of 1,2,4-trichlorobenzene with palladized nanoscale Fe0 particles supported on chitosan and silica, Chemosphere, 65(7), pp. 1137-1145.
Uwagi
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2019).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-defc29e5-a6fc-4102-b86e-d94221e2d52d