Analysis for Cd, Cu, Ni, Zn, and Mn in estuarine water by inductively coupled plasma mass spectrometry coupled with an automated flow injection system

被引:77
作者
Beck, NG
Franks, RP
Bruland, KW [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Ocean Sci, Santa Cruz, CA 95064 USA
[2] Univ Calif Santa Cruz, Dept Earth Sci, Santa Cruz, CA 95064 USA
[3] Univ Calif Santa Cruz, Inst Marine Sci, Santa Cruz, CA 95064 USA
关键词
trace metal analysis; seawater; ICP-MS; flow injection;
D O I
10.1016/S0003-2670(01)01561-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A flow injection inductively coupled plasma magnetic sector mass spectrometry (FI-ICP-MS) method was developed for the analysis of Cd, Cu, Ni, Zn, and Mn in estuarine waters. The method uses just greater than 3 ml sample, and employs an automated on-line preconcentration step using a metal chelating resin (Toyopearl AF-Chelate 650 M). Acidified samples for the analysis of Cd, Cu, Ni, and Zn were buffered on-line to pH of 5.6 +/- 0.2 with ammonia acetate just prior to loading onto the chelating resin, while samples for Mn analysis were adjusted to pH of 9.0 +/- 0.2 prior to concentration. Limits of detection were: Cd = 1.4 ng l(-1) (0.013 nM), Cu = 17 ng l(-1) (0.27 nM), Ni = 28 ng l(-1) (0.48 nM), Zn = 46 ng l(-1) (0.70 nM), and Mn = 86 ng l(-1) (1.6 nM). The blank concentrations were less than 1.5% of the SLEW-2 concentrations for each element analyzed, except Ni, which had a significant, but very constant blank from the Ni cones used. The detection limits were less than 5% of the concentrations observed in the San Francisco Bay estuarine samples, with the exception of Zn where the detection limit was 10% of the concentration of lowest San Francisco Bay sample analyzed. Using the FI preconcentration technique, we conducted medium resolution scans of potential isobaric interferences (mass units 55-66) using a magnetic sector ICP-MS to identify a number of interferent complications with evaluating certain isotopes. especially, Co-59, and Ni-60. Investigations of potential interferents illustrate the importance of appropriate isotope selection and, in some instances, the need to perform blank corrections with both an instrumental and a matrix blank. The method was verified by the analysis of an estuarine water standard reference materials (SLEW-2), and San Francisco Bay samples with previously reported values. Six estuarine samples run in triplicate generated the following average precision (presented as % R.S.D.); Cd = 4.2%, Cu = 3.2%, Ni = 3.3%, Zn = 4.4%, and Mn = 2.2%. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:11 / 22
页数:12
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