Efficiency of TiO(2) photocatalytic degradation of HHCB (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta[gamma]-2-benzopyran) in natural aqueous solutions by nested experimental design and mechanism of degradation

dc.contributor.authorCalza, P.en
dc.contributor.authorSakkas, V. A.en
dc.contributor.authorMedana, C.en
dc.contributor.authorIslam, M. A.en
dc.contributor.authorRaso, E.en
dc.contributor.authorPanagiotou, K.en
dc.contributor.authorAlbanis, T.en
dc.date.accessioned2015-11-24T16:57:29Z
dc.date.available2015-11-24T16:57:29Z
dc.identifier.issn0926-3373-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10584
dc.rightsDefault Licence-
dc.subjecttio(2)en
dc.subjectmineralizationen
dc.subjectnested designen
dc.subjectpersonal care productsen
dc.subjectwater treatment plantsen
dc.subjectpolycyclic musksen
dc.subjectwaste-wateren
dc.subjectrisk-assessmenten
dc.subjectunited-statesen
dc.subjectsuspensionsen
dc.subjectfateen
dc.subjectahtnen
dc.titleEfficiency of TiO(2) photocatalytic degradation of HHCB (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta[gamma]-2-benzopyran) in natural aqueous solutions by nested experimental design and mechanism of degradationen
heal.abstractThe present paper deals with the photocatalytic transformation of HHCB (1,3.4.6,7,8-hexahydro-4,6,6,7.8,8-hexamethylcyclopent[gamma]+2-benzopyran, trade name Galaxolide), under simulated solar irradiation using titanium dioxide as a photocatalyst. The investigation has involved a study of HHCB decomposition under a variety of experimental conditions, the identification of intermediate compounds, as well as the assessment of mineralization. A fully nested experimental design was applied to study the effect of various matrices (i.e. distilled water, surface water and wastewater) as well as the initial HHCB concentration on the variation of the photocatalytic efficiency. GC/MS and LC/MS were brought to bear in assessing the temporal course of the photocatalyzed process. A first pathway involves the hydroxylation, that is confined to the benzopyran moiety. Another route proceeds through the detachment of the hexamethylpentacycle moiety, with the formation of the ketoderivative. A parallel transformation involves benzopyran moiety with the ring cleavage. All the identified transformation products are degraded themselves until 2 h of irradiation, while complete mineralization is achieved until 8 h. (C) 2010 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.apcatb.2010.06.038-
heal.identifier.secondary<Go to ISI>://000281917200036-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0926337310002882/1-s2.0-S0926337310002882-main.pdf?_tid=9449275626db75e36184446d9031c732&acdnat=1333022731_89776b2ae6e59b682a16a5fe87b93d6e-
heal.journalNameApplied Catalysis B-Environmentalen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2010-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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