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Received June 10, 2008
Accepted August 7, 2008
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This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits
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Kinetic study and hydrogen peroxide consumption of phenolic compounds oxidation by Fenton’s reagent
Department of Chemical Engineering and Environment, University of the Basque Country, P.O.B. 644, 48080 Bilbao, Spain 1Department of Chemical Engineering, University of the Basque Country, P.O.B. 644, 48080 Bilbao, Spain
ana.deluis@ehu.es
Korean Journal of Chemical Engineering, January 2009, 26(1), 48-56(9)
https://doi.org/10.1007/s11814-009-0009-x
https://doi.org/10.1007/s11814-009-0009-x
Abstract
Synthetic solutions of phenol, o-, m- and p-cresol were oxidised by using Fenton’s reagent. The application of substoichiometric dosage of H2O2 led to the formation of intermediate compounds, continuing later the oxidation to complete oxidation. An important objective was to analyze the effect of hydrogen peroxide dosage applied and the reaction pH together with the iron oxidation state on the degradation level. A kinetic model was derived from a reaction mechanism postulated which was used to analyze the results of the experiments. Another aim was to analyze the hydrogen peroxide consumption. Noteworthy results include an increase in oxidant consumption to intensify phenol removal. Furthermore, oxidant consumption was analyzed through the ratio H2O2 to phenol removed and the average specific rate of removal (ASRR). By analyzing these two parameters it has been possible to ascertain the most favorable strategy for an efficient application of H2O2.
Keywords
References
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Rao L, Kanmani S, Indian J. of Environ. Prot., 26, 619 (2006)
Sedlak DL, Andren AW, Environ. Sci. Technol., 25, 777 (1991)
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Bishop DF, Stern G, Fleischman M, Marshall LS, Ind. Eng. Chem. Process Design Dev., 7, 110 (1968)
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Kang N, Lee D, Yoon J, Chemosphere, 47, 915 (2002)
Lunak S, Sedlak P, J. of Photoch. Photobio. A, 68, 1 (1992)
Zazo JA, Casas JA, Molina CB, Quintanilla A, Rodriguez JJ, Environ. Sci. Technol., 41, 7164 (2007)
Hong SH, Kwon BH, Lee JK, Kim IK, Korean J. Chem. Eng., 25(1), 46 (2008)
Kolthoff IM, Medalia AI, J. Am. Chem. Soc., 71, 3777 (1949)
Pera-Titus M, Garcia-Molina V, Banos MA, Gimenez J, Esplugas S, Appl. Catal. B: Environ., 47(4), 219 (2004)
Yavuz Y, Koparal AS, Ogutveren UB, Chem. Eng. Technol., 30(5), 583 (2007)
Sanz J, Lombrana JI, De Luis A, Ortueta M, Varona F, Environ. Chem. Lett., 1, 45 (2003)
Eisenberg GM, Ind. Eng. Chem., 15, 327 (1942)
Guittonneau S, de Laat J, Dore M, Duguet JP, Bonnel C, Environ. Technol. Lett., 9, 1115 (1988)
Masschelein WJ, Denis M, Lendent R, Water and Sewage Works, 8, 69 (1977)
Striolo P, Debelle H, Foussard JN, Tribune de l’eau., 556 (1992)
Anbar M, Meyerstein D, Neta P, J. Phys. Chem. A, 70, 2660 (1966)
Litvintsev IY, Mikhailyuk AI, Sapunov VN, Kinet. Catal., 36, 482 (1995)
Benitez FJ, Beltranheredia J, Gonzalez T, Real F, Ind. Eng. Chem. Res., 34(11), 4099 (1995)
de Luis A, Lombrana JI, Menendez A, J. Adv. Oxid. Technol., 11, 21 (2008)
Montaser YG, Hartel G, Mayer R, Haseneder R, Waste Manage., 21, 41 (2001)
Kavitha V, Palanivelu K, Chemosphere, 55, 1235 (2004)
Martinez F, Calleja G, Melero JA, Molina R, Appl. Catal. B: Environ., 70(1-4), 452 (2007)
Kavitha V, Palanivelu K, Water Res., 39, 3062 (2005)
de Asin K, Dutta BK, Bhattacharjee S, Environ. Prog., 25, 64 (2006)
Nicell JA, Wright H, Enzyme Microb. Technol., 21(4), 302 (1997)
Glaze WH, Lay Y, Kang JW, Ind. Eng. Chem. Res., 34(7), 2314 (1995)
Karpel N, Dore M, Wat. Res., 31, 1383 (1997)
Lombrana JI, Varona F, Martinez C, de Luis A, Recent Res. Devel. In Chemical Engg., 1, 41 (1997)

