A comparison between ICP-MS and AFS detection for arsenic speciation in environmental samples

被引:202
作者
Gómez-Ariza, JL [1 ]
Sánchez-Rodas, D [1 ]
Giráldez, I [1 ]
Morales, E [1 ]
机构
[1] Univ Huelva, Escuela Politecn Super, Dept Quim & Ciencia Mat, Palos De La Frontera 21819, Huelva, Spain
关键词
arsenic speciation; atomic fluorescence spectrometry; inductively coupled plasma-mass spectrometry;
D O I
10.1016/S0039-9140(99)00257-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Performances of two atomic detectors, Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) arid Atomic Fluorescence Spectrometry (AFS) have been compared for arsenic speciation in environmental samples. Instrumental couplings, based on the use of high performance liquid chromatography (HPLIC), hydride generation (HG), and the two atomic detectors were used for the speciation of arsenite, arsenate, dimethylarsinic acid and monomethylarsonic acid. Optionally, arsenobetaine was also determined using on-line ultraviolet (UV) photooxidation. The detection limits ranging from 0.1 to 0.3 mu g 1(-1) (as As) and the precision > 10% RSD obtained with HPLC-(UV)-HG-AFS were comparable with those obtained with HPLC-(UV)-HG-ICP-MS. Both instrumental coupling were applied to the NRCC-TORT-1 and several environmental samples, such as seawater, freshwater, sediments, bivalves and bird eggs, taken from two areas with different degrees of pollution. No influence of the sample matrix was observed on the results using external calibration and standard additions met:hods, for both coupled techniques. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:257 / 268
页数:12
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