Evaluation of heterogeneous photo-Fenton oxidation of Orange II using response surface methodology

A mesoporous SBA-15 doped iron oxide (Fe2O3/SBA-15) was synthesized by co-condensation, characterized and used as heterogeneous catalysts for the photo-Fenton decolorization of azo dye Orange II under UV irradiation. Response surface methodology (RSM) was used to investigate operating condition effe...

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Publié dans:Water science and technology : a journal of the International Association on Water Pollution Research. - 1986. - 62(2010), 6 vom: 23., Seite 1320-6
Auteur principal: Gong, Y H (Auteur)
Autres auteurs: Zhang, H, Li, Y L, Xiang, L J, Royer, S, Valange, S, Barrault, J
Format: Article en ligne
Langue:English
Publié: 2010
Accès à la collection:Water science and technology : a journal of the International Association on Water Pollution Research
Sujets:Journal Article Research Support, Non-U.S. Gov't Azo Compounds Benzenesulfonates Fenton's reagent Ferric Compounds SBA-15 Water Pollutants, Chemical ferric oxide 1K09F3G675 plus... Silicon Dioxide 7631-86-9 Hydrogen Peroxide BBX060AN9V Iron E1UOL152H7 2-naphthol orange Q1LIY3BO0U
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Résumé:A mesoporous SBA-15 doped iron oxide (Fe2O3/SBA-15) was synthesized by co-condensation, characterized and used as heterogeneous catalysts for the photo-Fenton decolorization of azo dye Orange II under UV irradiation. Response surface methodology (RSM) was used to investigate operating condition effects, such as hydrogen peroxide concentration, initial pH and catalyst loadings, on the decolorization rate. UV irradiation is found to enhance the activity of the catalyst in the process. RSM analysis evidenced the influence of the initial pH value and H2O2 concentration on the dye degradation rate. The coupled UV/Fe2O3/SBA-15/H2O2 process at room temperature is revealed as a promising friendly process for wastewater treatment. Indeed, the use of a heterogeneous catalyst allows an easy active phase recycling without multi-step recovering while the heterogeneous catalyst used here exhibits high catalytic activity for the reaction considered
Description:Date Completed 10.12.2010
Date Revised 25.11.2016
published: Print
Citation Status MEDLINE
ISSN:0273-1223
DOI:10.2166/wst.2010.432