An integrated gas chromatographic method towards the simultaneous determination of phosphoric and amino acid group containing pesticides

dc.contributor.authorStalikas, C. D.en
dc.contributor.authorPilidis, G. A.en
dc.contributor.authorKarayannis, M. I.en
dc.date.accessioned2015-11-24T16:48:31Z
dc.date.available2015-11-24T16:48:31Z
dc.identifier.issn0009-5893-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9333
dc.rightsDefault Licence-
dc.subjectgas chromatography - mass spectrometryen
dc.subjectfluoroacetylation and fluoroethylesterificationen
dc.subjectphosphoric and amino acid-type pesticidesen
dc.subjectcolumn liquid-chromatographyen
dc.subjectflame photometric detectionen
dc.subject(aminomethyl)phosphonic aciden
dc.subjectaminomethylphosphonic aciden
dc.subjectherbicides glyphosateen
dc.subjectrapid-determinationen
dc.subjectmass-spectrometryen
dc.subjectwateren
dc.subjectglufosinateen
dc.subjectderivatizationen
dc.titleAn integrated gas chromatographic method towards the simultaneous determination of phosphoric and amino acid group containing pesticidesen
heal.abstractAmpropylfos, glyphosate, glufosinate and bialaphos are water soluble pesticides that contain phosphoric and amino acid groups in their molecules. Their polar nature and high water solubility make extraction difficult and limit the options for using the various derivatization techniques often employed for gas chromatographic analysis. A multiresidue method is proposed that allows the simultaneous determination of six analytes (pesticides and some of their metabolites) in environmental waters down to sub-mu g L-1 levels. A mixture of trifluoroacetic anhydride and trifluoroethanol converts them in a single-step reaction to derivatives that are sufficiently volatile for gas chromatographic analysis. Electron capture and mass-selective detection are used for quantitation purposes, and their analytical characteristics are presented. Under the chromatographic conditions employed, acceptable separation is attained for the derivatized analytes, with both glufosinate and bialaphos emerging as double peaks. Recoveries of spiked environmental water samples range from 88 to 106%. The mean relative standard deviation of the method does not exceed 3.0%, whereas, depending on the detection system, the limits of detection for the analytes are in the range of 0.09-65 mu g L-1, the upper value being the bialaphos detection limit.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1007/BF02505414-
heal.identifier.secondary<Go to ISI>://000088096900013-
heal.identifier.secondaryhttp://www.springerlink.com/content/k722h246801575n8/fulltext.pdf-
heal.journalNameChromatographiaen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2000-
heal.publisherFriedr. Vieweg & Sohn Verlagsgesellschaften
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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