Differentiation and quantification of linear alkyl benzenesulfonate isomers by liquid chromatography-ion-trap mass spectrometry

被引:21
作者
Lunar, L [1 ]
Rubio, S [1 ]
Pérez-Bendito, D [1 ]
机构
[1] Edificio Anexo Marie Curie, Fac Ciencias, Dept Analyt Chem, E-14071 Cordoba, Spain
关键词
positional isomers; atkyl benzenesulfonates; linear; surfactants;
D O I
10.1016/j.chroma.2003.08.071
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Discrimination and quantitation of the 20 positional isomers Of C-10-C-13 linear alkyl benzenesulfonates (LASs), based on the use of reversed-phase liquid chromatography-electrospray ionisation in negative ion mode ion-trap mass spectrometry, was undertaken. Discrimination was achieved by LAS MS-MS analysis into the ion trap, by monitoring specific fragment ions resulting from the benzylic cleavage of the carbon alkyl chain on both side of the LAS phenyl group. Parameters affecting the electrospray ionisation source and the ion-trap operation were optimised. Calibration curves for the different isomers were established and this permitted their quantitation by mass spectrometry for the first time. MS-MS responses were dependent on both the position of the phenyl group on the alkyl chain and the length of this alkyl chain, these responses being higher for the external isomers and the longer alkyl chain homologues. The precision, expressed as relative standard deviation ranged between 9 and 13%. Detection limits for LAS isomers were between 0.03 and 0.07 mg/l and therefore the method is sensitive enough to be applied to environmental samples. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 25
页数:9
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