Determination of diethylhexyladipate and acetyltributylcitrate in aqueous extracts after cloud point extraction coupled with microwave assisted back extraction and gas chromatographic separation

dc.contributor.authorZygoura, P. D.en
dc.contributor.authorPaleologos, E. K.en
dc.contributor.authorRiganakos, K. A.en
dc.contributor.authorKontominas, M. G.en
dc.date.accessioned2015-11-24T16:55:33Z
dc.date.available2015-11-24T16:55:33Z
dc.identifier.issn0021-9673-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10325
dc.rightsDefault Licence-
dc.subjectcloud point extractionen
dc.subjectdehaen
dc.subjectatbcen
dc.subjectmicrowave back extractionen
dc.subjectgas chromatographyen
dc.subjectsolid-phase microextractionen
dc.subjectperformance liquid-chromatographyen
dc.subjectpreconcentration step prioren
dc.subjectphthalic-acid estersen
dc.subjectcapillary-electrophoresisen
dc.subjectorganic pollutantsen
dc.subjectmicellar solutionsen
dc.subjectplasticized pvcen
dc.subjectwater samplesen
dc.subjectfooden
dc.titleDetermination of diethylhexyladipate and acetyltributylcitrate in aqueous extracts after cloud point extraction coupled with microwave assisted back extraction and gas chromatographic separationen
heal.abstractThe determination of commercial plasticizers (di-(2-ethylhexyl)adipate (DEHA) and acetyl tributyl citrate (ATBC)) in aqueous solutions is described. The newly proposed technique of applying microwaves to cloud point extracts in order to enable combination with gas chromatographic analysis has been used for this purpose. Both plasticizers were entrapped in the micelles of the non-ionic surfactant Triton X-114 and removed from the bulk phase by centrifugation. Micellization was enhanced by increasing the ionic strength of the solution with concentrated NaCl. Extraction recoveries of the proposed method were over 95% for water and 3% (w/v) aqueous acetic acid and over 85% for 10% (v/v) aqueous ethanol, respectively. The calibration curves obtained, following the proposed methodology have a linear range between 50 and 2000 mu g/L for each analyte while the detection limits were as low as 15 and 19 mu g/L for DEHA and ATBC, respectively, with an RSD below 5% even for low concentrations. As an analytical demonstration the proposed methodology was applied for the determination of the migration levels of the selected plasticizers from a PVC food packaging film into aqueous simulants. (c) 2005 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.chroma.2005.07.075-
heal.identifier.secondary<Go to ISI>://000232957900004-
heal.identifier.secondaryhttp://ac.els-cdn.com/S002196730501575X/1-s2.0-S002196730501575X-main.pdf?_tid=bf8c4ad06bd485755c577f83106ac2e3&acdnat=1333037762_430dc6d561ce9c69c9b2a337abe903ed-
heal.journalNameJournal of Chromatography Aen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2005-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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