Application of solvent microextraction in a single drop for the determination of new antifouling agents in waters

dc.contributor.authorLambropoulou, D. A.en
dc.contributor.authorAlbanis, T. A.en
dc.date.accessioned2015-11-24T16:52:33Z
dc.date.available2015-11-24T16:52:33Z
dc.identifier.issn0021-9673-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9904
dc.rightsDefault Licence-
dc.subjectwater analysisen
dc.subjectsolvent microextractionen
dc.subjectantifouling booster biocidesen
dc.subjectchlorothalonilen
dc.subjectdichlofluaniden
dc.subjectsea nine 211en
dc.subjectsolid-phase microextractionen
dc.subjectpaint booster biocidesen
dc.subjectlinked-immunosorbent-assayen
dc.subjectgas-chromatographyen
dc.subjectconventional microsyringeen
dc.subjectnitroaromatic explosivesen
dc.subjectmass-spectrometryen
dc.subjectmarine-sedimentsen
dc.subjectseawater samplesen
dc.subjectnatural-watersen
dc.titleApplication of solvent microextraction in a single drop for the determination of new antifouling agents in watersen
heal.abstractA new, rapid microextraction technique termed solvent microextraction (SME) has been developed for the simultaneous determination of new generation antifouling agents, in water samples. Chlorothalonil, dichlofluanid and Sea nine 211 were employed as model compounds to asses the extraction procedure and were determined by gas chromatography with electron capture detection. Experimental parameters which control the performance of SME, such as selection of solvent, exposure time, agitation, organic drop volume, and salt concentration were optimized. The new method provided good average enrichment factors of >10.7 for all analytes, good precision (RSD < 8.5%) and good linearity (r(2) > 0.9880). The limits of detection (LODs) were in the range of 0.00025-0.003 mug/L (S/N = 3). The SME was performed in different type of natural water samples and acceptable recoveries were obtained for the tested analytes. The results demonstrated that SME is a rapid, accurate and effective preparation method and could be successfully performed for the determination of antifouling agents in water samples. (C) 2004 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.chroma.2004.08.024-
heal.identifier.secondary<Go to ISI>://000224165300003-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0021967304013536/1-s2.0-S0021967304013536-main.pdf?_tid=25dfcaf8b45289d302ebbde72ee0735b&acdnat=1333023094_cd56589518efed08c83a511000b0b462-
heal.journalNameJournal of Chromatography Aen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2004-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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