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Título

Determination of phthalic monoesters in aqueous and urine samples by solid-phase microextraction-diazomethane on-fibre derivatization-gas chromatography-mass spectrometry

AutorAlzaga Morales, Roberto; Peña, Araceli; Bayona Termens, Josep María CSIC ORCID
Palabras claveSPME
On-fibre derivatization
Phthalate monoesters
GC–MS
Urine
Landfill leachates
Wastewater
Fecha de publicación28-ene-2003
EditorWiley-Blackwell
CitaciónJournal of Separation Science 26(1-2): 87-96 (2003)
ResumenA solvent-free analytical methodology for the determination of phthalic monoesters (MPs) with diazomethane on-fibre derivatization using solid-phase microextraction–gas chromatography–mass spectrometry (SPME–DOFD–GC–MS) was developed. Among the different SPME fibres evaluated, the polydimethylsiloxane/divinylbenzene (PDMS/DVB) proved to be the most suitable for the determination of four MPs. diazomethane on-fibre derivatization (DOFD) procedure was improved, avoiding diethyl ether as solvent. Equilibrium conditions were reached (15 min) and K9MP values were calculated. Under optimum MP extraction conditions (e. g. direct immersion, 4 mL of sample, 258C extraction temperature, stirring at 1100 rpm, 20 min extraction time, 10 min derivatization reaction, and pH = 1.5), trace level concentrations of MPs (0.3–8.6 ng/mL) were detected, allowing the simultaneous determination of phthalic diesters (DPs). The overall SPME–GC–MS precision was improved by using deuterated internal standards. The developed analytical methodology was applied different environmental water matrices and human urine samples at MP concentrations ranging from 0.1–538 ng/mL. The developed analytical procedure is robust analyses with the same fibre), rapid (40 min), and of low cost, improving the conventional analysis methods in terms of analysis time, background levels, and cost.
Descripción10 pages, 4 figures, 4 tables.-- Printed version published Jan 2003.
Versión del editorhttp://dx.doi.org/10.1002/jssc.200390020
URIhttp://hdl.handle.net/10261/19916
DOI10.1002/jssc.200390020
ISSN1615-9306
E-ISSN1615-9314
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