Direct determination of trace elements in sea-water using reaction cell inductively coupled plasma mass spectrometry

被引:64
|
作者
Louie, H
Wu, M
Di, P
Snitch, P
Chapple, G
机构
[1] Australian Govt Analyt Labs, Pymble, NSW 2073, Australia
[2] Perkin Elmer Corp, N Ryde, NSW 2113, Australia
[3] Wollongbar Agr Inst, Wollongbar, NSW 2477, Australia
关键词
D O I
10.1039/b109121m
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method is described for the direct determination of several transition elements in sea-water by reaction cell (RC)-inductively coupled plasma mass spectrometry (ICP-MS) using ammonia as a reaction gas. Results show significant improvement over standard quadrupole (Q) ICP-MS performance for direct sea-water analysis and were comparable to high resolution (HR) ICP-MS. In this study, the RC-ICP-MS was used to determine chromium, copper, manganese, nickel and vanadium in sea-water. Ammonia gas was passed through the reaction cell to reduce molecular ion interference. These interferences normally lead to false positive results when low resolution quadrupole ICP-MS (Q-ICP-MS) is used to analyze sea-water. Good recoveries were obtained for V-51, Cr-52 and Mn-55 in the 1 : 10 diluted sea-water, CASS-4, NASS-4 and SLEW-3. Molecular ion interference was reduced significantly but not completely for Ni-58 and Cu-63, giving rise to a positive bias typically no more than 0.3 mug l(-1). A matrix blank subtraction or matrix matched external calibration can be used to further improve the accuracy for these elements at levels below 0.5 mug l(-1). Detection limits in the undiluted sea-water range from 0.02 mug l(-1) for chromium to 0.3 mug l(-1) for copper. The precision and accuracy of the method were checked against three certified reference standards.
引用
收藏
页码:587 / 591
页数:5
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