H2O2/TiO2 Photocatalytic Oxidation of Metol. Identification of Intermediates and Reaction Pathways

dc.contributor.authorAceituno, M.en
dc.contributor.authorLunar, L. M.en
dc.contributor.authorStalikas, C. D.en
dc.contributor.authorRubio Bravo, S.en
dc.contributor.authorPerez Bendito, M. D.en
dc.date.accessioned2015-11-24T16:38:33Z
dc.date.available2015-11-24T16:38:33Z
dc.identifier.issn0043-1354-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8059
dc.rightsDefault Licence-
dc.subjectMetolen
dc.subjectPhotographic developersen
dc.subjectAdvanced oxidation processen
dc.subjectTitanium dioxide photocatalytic oxidationen
dc.subjectHydrogen peroxide oxidationen
dc.titleH2O2/TiO2 Photocatalytic Oxidation of Metol. Identification of Intermediates and Reaction Pathwaysen
heal.abstractThe applicability of H2O2 to increase the efficiency of TiO2 photocatalytic degradations was investigated. The photographic developer metol [N-methyl-p-aminophenol] that does not adsorb on the surface of TiO2 particulates was used as a model for this purpose. It was proved that metol was mineralised under oxidation with H2O2/TiO2/UV through different thermal and photochemical reactions. Identification of intermediates by both HPLC-electron impact-MS and HPLC-electrospray ionisation-MS helped to elucidate the role of H2O2 and TiO2 in the degradation process and to establish degradation pathways. Intermediates yielded were partially oxygenated aromatic species and dimers, which were amenable to oxidation. The optimal degradation conditions found for mineralisation were 0.4M H2O2, 5 mg/ml TiO2, pH 9 and irradiation centred at 360nm (4.9mW/cm2). The use of oxidants opens an interesting medium to the treatment of effluents containing a diversity of organics since they increase substantially the efficiency of TiO2 photocatalytic degradations.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.sciencedirect.com/science/article/pii/S0043135402000611#-
heal.journalNameWater Resen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2002-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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