Photocatalytic degradation of selected s-triazine herbicides and organophosphorus insecticides over aqueous TiO2 suspensions

dc.contributor.authorKonstantinou, I. K.en
dc.contributor.authorSakellarides, T. M.en
dc.contributor.authorSakkas, V. A.en
dc.contributor.authorAlbanis, T. A.en
dc.date.accessioned2015-11-24T16:44:34Z
dc.date.available2015-11-24T16:44:34Z
dc.identifier.issn0013-936X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8816
dc.rightsDefault Licence-
dc.subjectchromatography-mass-spectrometryen
dc.subjectliquid-chromatographyen
dc.subjectgas-chromatographyen
dc.subjectphotolysis productsen
dc.subjectantifouling paintsen
dc.subjecthydrogen-peroxideen
dc.subjecttitanium-dioxideen
dc.subjectwater treatmenten
dc.subjectoxidationen
dc.subjectidentificationen
dc.titlePhotocatalytic degradation of selected s-triazine herbicides and organophosphorus insecticides over aqueous TiO2 suspensionsen
heal.abstractThe photocatalytic degradation of selected s-triazine herbicides and organophosphorus insecticides was carried out in aqueous TiO2 suspensions under simulated solar light. The tested herbicides from the s-triazines group were atrazine, propazine, cyanazine, prometryne, and irgarol. The tested insecticides from the organophosphorus group were ethyl parathion, methyl parathion, ethyl bromophos, methyl bromophos, and diclofenthion. Degradation kinetics followed first-order reaction and has been monitored through gas chromatography. The degradation was fast with half-lives varying from 10.2 to 38.3 min depending on the nature and the structure of compounds. The generated transformation products (TPs) were formed via oxidation, dealkylation, and dechlorination for s-triazines and via oxidation and photohydrolysis for organophosphates. The TPs of irgarol, bromophos, and dichlofenthion were identified using solid-phase extraction (SDB-disks) and GC-MS techniques, and possible degradation routes were proposed showing similar degradation pathways as for other triazines and organophosporus pesticides. This work points out to the necessity of extended knowledge of the successive steps in a solar-assisted detoxification process.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1021/Es001271c-
heal.identifier.secondary<Go to ISI>://000166390700023-
heal.identifier.secondaryhttp://pubs.acs.org/doi/pdfplus/10.1021/es001271c-
heal.journalNameEnviron Sci Technolen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2001-
heal.publisherAmerican Chemical Societyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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