Determination of linear alkylbenzensulfonates in aqueous matrices by ion-pair solid-phase microextraction-in-port derivatization-gas chromatography-mass spectrometry
被引:40
作者:
Alzaga, R
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机构:IIQAB, CSIC, Dept Environm Chem, Barcelona 08034, Spain
Alzaga, R
Peña, A
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h-index: 0
机构:IIQAB, CSIC, Dept Environm Chem, Barcelona 08034, Spain
Peña, A
Ortiz, L
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机构:IIQAB, CSIC, Dept Environm Chem, Barcelona 08034, Spain
Ortiz, L
Bayona, JM
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h-index: 0
机构:IIQAB, CSIC, Dept Environm Chem, Barcelona 08034, Spain
Bayona, JM
机构:
[1] IIQAB, CSIC, Dept Environm Chem, Barcelona 08034, Spain
[2] Univ Nacl Autonoma Mexico, Dept Analyt Chem, Fac Chem, Mexico City 04510, DF, Mexico
water analysis;
derivatization;
GC;
environmental analysis;
alkyl benzenesulfonates;
linear;
surfactants;
D O I:
10.1016/S0021-9673(03)00493-X
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Trace determination (low ng/ml) of linear alkylbenzensulfonates (LASs) in water was achieved by solid-phase microextraction (SPME) of ion-pairs formed with tetrabutylammonium. This ion-pairing reagent served two purposes. First, it allowed the extraction of LAS with the polydimethylsiloxane fiber by counterion association and second, the derivatization of the formed LAS ion pairs in the GC injection port at 300 degreesC to form the corresponding sulfonated butyl esters. The methodology developed allows the isomer specific determination of LAS at low detection limits (0.16-0.8 ng/ml), depending on the alkyl chain lengths of LASs with RSDs of 10-12%. Furthermore, the developed methodology was applied to urban wastewater and sea water and compared with a solid-phase extraction (SPE) method (e.g. C-18 and strong anion-exchange sorbent) to obtain concordant values for urban wastewater. Moreover, the developed SPME methodology overcame the procedural blank and matrix-dependent recoveries found in the SPE methodologies at low LAS concentrations. (C) 2003 Elsevier Science B.V. All rights reserved.