Aqueous phototransformation of zinc pyrithione - Degradation kinetics and byproduct identification by liquid chromatography-atmospheric pressure chemical ionisation mass spectrometry

dc.contributor.authorSakkas, V. A.en
dc.contributor.authorShibata, K.en
dc.contributor.authorYamaguchi, Y.en
dc.contributor.authorSugasawa, S.en
dc.contributor.authorAlbanis, T.en
dc.date.accessioned2015-11-24T16:52:39Z
dc.date.available2015-11-24T16:52:39Z
dc.identifier.issn0021-9673-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9914
dc.rightsDefault Licence-
dc.subjectphotodegradationen
dc.subjectzinc pyrithioneen
dc.subjectdissolved organic matteren
dc.subjectfateen
dc.subjectdissolved organic-matteren
dc.subjectpaint booster biocidesen
dc.subjectnatural-watersen
dc.subjectenvironmental fateen
dc.subjectphotolysisen
dc.subjectbehavioren
dc.subjectnitrateen
dc.titleAqueous phototransformation of zinc pyrithione - Degradation kinetics and byproduct identification by liquid chromatography-atmospheric pressure chemical ionisation mass spectrometryen
heal.abstractThe photochemical behavior of the antifouling agent zinc pyrithione (ZnPT) was studied in aqueous media of different composition under simulated solar irradiation using a xenon light source. The influence of important constituents of natural water (dissolved organic matter and nitrate) was also examined using a multivariate kinetic model. It was found that photodegradation proceeds via a pseudo first-order reaction. Kinetic experiments were monitored by LC-MS and photolytic half-lives ranging between 9.2 and 15.1 min have been observed. The increasing concentration of dissolved organic matter (DOM) accelerates the photolysis reaction, while the effect of nitrate ions was also positive since it increased the degradation rate, but to a lesser extent. Irradiation of the aqueous ZnPT solutions gave rise to several transformation products that were isolated by means of solid-phase extraction using poly(styrene-divinylbenzene) extraction disks. These byproducts were identified using liquid chromatography-atmospheric pressure chemical ionisation mass spectrometry. Besides 2-pyridinesulfonic-acid, other degradation products formed included pyridine-N-oxide, 2-mercaptopyridine, 2,2'-dithiobis(pyridine-N-oxide), 2,2-dipyridyl disulfide and the pyridine/pyrithione mixed disulfide, 2,2'-dithiobispyridine mono-N-oxide (PPMD). (c) 2007 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.chroma.2007.01.049-
heal.identifier.secondary<Go to ISI>://000245004100003-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0021967307000544/1-s2.0-S0021967307000544-main.pdf?_tid=8c5828646c950426dc113fe267062dc8&acdnat=1333023418_ab7ca9c52affd5a181045479223c3f9e-
heal.journalNameJournal of Chromatography Aen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2007-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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