Determination of uranium in tap water by ICP-MS

被引:37
作者
El Himri M. [1 ,2 ]
Pastor A. [1 ]
De La Guardia M. [1 ]
机构
[1] Department of Analytical Chemistry, University of Valencia, 50 Dr. Moliner St.
[2] University of Oujda, Dep. Anal. Chem., Route Sidi Mâafa
来源
Fresenius' Journal of Analytical Chemistry | 2000年 / 367卷 / 2期
关键词
Uranium; Mass Spectrometer; Relative Standard Deviation; Mineral Water; Couple Plasma Mass;
D O I
10.1007/s002160051616
中图分类号
学科分类号
摘要
A fast and accurate procedure has been developed for the determination of uranium at μg L-1 level in tap and mineral water. The method is based on the direct introduction of samples, without any chemical pre-treatment, into an inductively coupled plasma mass spectrometer (ICP-MS). Uranium was determined at the mass number 238 using Rh as internal standard. The method provides a limit of detection of 2 ng L-1 and a good repeatability with relative standard deviation values (RSD) about 3% for five independent analyses of samples containing 73 μg L-1 of uranium. Recovery percentage values found for the determination of uranium in spiked natural samples varied between 91% and 106%. Results obtained are comparable with those found by radiochemical methods for natural samples and of the same order for the certified content of a reference material, thus indicating the accuracy of the ICP-MS procedure without the need of using isotope dilution. A series of mineral and tap waters from different parts of Spain and Morocco were analysed. © Springer-Verlag 2000.
引用
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页码:151 / 156
页数:5
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