Rapid and accurate determination of Thallium in seawater using SF-ICP-MS

被引:21
作者
Boening, Philipp [1 ]
Schnetger, Bernhard [1 ]
机构
[1] Carl von Ossietzky Univ Oldenburg, Inst Chem & Biol Meeres ICBM, D-26111 Oldenburg, Germany
关键词
Marine chemistry; Thallium; Environment; Monitoring; ICP-MS; PLASMA-MASS SPECTROMETRY; WATER SAMPLES; SEA-WATER;
D O I
10.1016/j.talanta.2011.06.031
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We present a method for the rapid and direct determination of dissolved Thallium (Tl) using high resolution sector field inductively coupled mass spectrometry (SF-ICP-MS) suitable for the measurement of large time series (e.g. during monitoring). Thallium data are presented for a series of natural sea water samples, which were validated with sea water standards CASS-4 and NASS-5. The sea water samples and standards were diluted 10 times prior to measurement with SF-ICP-MS in low resolution mode (R=300, LR). For both CASS-4 and NASS-5 (salinity of 30.5) we calculated a concentration of about 11 ng L(-1) when using TI values of 14 +/- 2 ng L(-1) (at salinity of 35 +/- 1) published by Flegal and Patterson [1] for Atlantic and Pacific sea water. For CASS-4 we report a Tl value of 10.6 +/- 0.7 ng L(-1) (n=70), for NASS-5 a Tl value of 10.3 +/- 0.8 ng L(-1) (n = 11). For Tl in both CASS-4 and NASS-5, the overall error in accuracy and precision is less than 4% and 8% (2 s), respectively. Further, values of 7.7 +/- 0.3 and 6.7 +/- 0.2 ng L(-1) Tl were found for the estuarine standard SLEW-3 (salinity of 15) and the river water standard SLRS-4, respectively, for which no certified value exists so far. The detection and quantification limits of our method are 0.1 and 0.3 ng L(-1), respectively. Slight differences in the accuracy of our method and other published methods for the determination of TI in sea water are discussed. Time-series of natural coastal water samples gave Tl values (6-12 ng L(-1)), which correspond to determined salinities, and hence, appear realistic and oceanographically consistent. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1695 / 1697
页数:3
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