Degradation of octylbenzene sulfonate photoi.nduced by iron(III) aquacoxnplexes: Evidence for the fragmentation of the alkyl chain
Autor: | Debbache, Nadra, Mailhot, Gilles, Djebbar, Kamel, Lavedrine, Bernadette, Bolte, Michèle |
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Přispěvatelé: | Laboratoire des Sciences et Technologies de l Environnement. (LSTE), Université frères Mentouri Constantine I (UMC), Photochimie moléculaire et macromoléculaire (PMM), Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie de Clermont-Ferrand (ICCF), Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-SIGMA Clermont (SIGMA Clermont)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université Mentouri Constantine [Algérie] (UMC) |
Jazyk: | angličtina |
Rok vydání: | 2005 |
Předmět: | |
Zdroj: | International Journal of Photoenergy International Journal of Photoenergy, 2005, 07, pp.71-78 International Journal of Photoenergy, Hindawi Publishing Corporation, 2005, 07, pp.71-78 |
ISSN: | 1110-662X |
Popis: | The degradation of octylbenzene sulfonate (OBS) photoinduced by iron(III) aquacomplexes was investigated upon irradiation at 365 nm and by solar light. The photochemical degradation appears to be due to HO* radicals arising from the electron transfer in Fe(OH)z`. If oxygen does not affect the initial quantum yield of OBS degradation, it is necessary to pursue the reaction op to, first the complete disappearance of OBS and secondly OBS mineralization. The nature of the major photoproducts gives evidence for a competitive attack of HO' radîcals on the allcyl chain resulting in a shortening of the chain. Among the possible sites on the chain, hydrogen on the carbon in a position with respect to the aromatic ring was the main point of attack with the formation of 4-acetylbenzene sulfonate and 4-carboxylicbenzene sulfonate. |
Databáze: | OpenAIRE |
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