Determination of arsenic and selenium species in groundwater and soil extracts by ion chromatography coupled to inductively coupled plasma mass spectrometry

被引:78
作者
Vassileva, E [1 ]
Becker, A [1 ]
Broekaert, JAC [1 ]
机构
[1] Univ Leipzig, Inst Analyt Chem, D-04103 Leipzig, Germany
关键词
arsenic speciation; selenium speciation; anion-exchange; inductively coupled plasma mass spectrometry; groundwater; soil extracts;
D O I
10.1016/S0003-2670(01)01089-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A procedure for the separation and determination of the five arsenic species As(IH), As(V), monomethylarsonic acid, dimethylarsinic acid and arsenobetain by ion chromatography coupled to inductively coupled plasma mass spectrometry under the use of anion exchange is described. It has been successfully applied to the analysis of groundwater and extracts of contaminated soils. No interference of Ar-40, Cl-35 and As-75 was observed when natural water samples were analyzed. The procedure shows good repeatability and accuracy in addition to easy handling. Detection limits for the arsenic species are in the range 0.4-0.8 mug l(-1). A detection limit of 4 mug l(-1) was obtained for the selenium species. Interference by Cl- up to concentrations of 400 mg l(-1) can be neglected. The influence of several parameters (eluent concentration, amount of methanol in the mobile phase, flow rate) has been studied so as to optimize the best chromatographic conditions. The procedure has prospects for environmental biomonitoring using a sensitive and efficient determination of arsenic and selenium species, as shown for groundwater samples spiked at the 50 pg l(-1) level. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:135 / 146
页数:12
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