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Determination of uranium and thorium in natural waters with a high matrix concentration using solid-phase extraction inductively coupled plasma mass spectrometry
被引:74
作者:
Unsworth, ER
Cook, JM
Hill, SJ
[1
]
机构:
[1] Univ Plymouth, Dept Environm Sci, Plymouth Environm Res Ctr, Plymouth PL4 8AA, Devon, England
[2] British Geol Survey, Keyworth NG12 5GG, Notts, England
基金:
英国工程与自然科学研究理事会;
关键词:
uranium;
solid-phase extraction;
ICP-MS;
dissolved organic carbon;
thorium;
D O I:
10.1016/S0003-2670(01)01138-2
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
An on-line solid-phase extraction method, linked to inductively coupled plasma mass spectrometry has been developed to overcome the problems of a high sample matrix concentration interfering with the determination of low levels of uranium and thorium in aqueous samples. Using an actinide-specific extraction resin (TRU-spec), in a small column incorporated into the sample introduction manifold, recovery of the analytes (U-101 - 108%, Th-87 115%) was obtained from seawater (NASS-4 seawater CRM, 2.68 ng ml(-1) U), ground water (0.1 ng ml(-1) U in 3000 mug ml(-1) total dissolved solids) and samples containing significant levels of dissolved organic carbon (1 ng ml(-1) U/Th, 8 mug ml(-1) humic and fulvic acids). This is an improvement on conventional ion exchange and chelating resins which give low recoveries in the presence of dissolved organic carbon. The samples were injected directly on to the column, with no prior dilution. Figures-of-merit obtained were R-2: U 0.998, Th 0.999, for 0 to 10 ng ml(-1), R.S.D.: U 4.3%, Th 5.8%, and limits of detection: U 0.015 ng ,ml(-1) and Th 0.006 ng ml(-1) in a synthetic seawater matrix. (C) 2001 Elsevier Science B.V. All rights reserved.
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页码:141 / 146
页数:6
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