Online standard additions calibration of transient signals for inductively coupled plasma mass spectrometry

被引:19
作者
Antler, Margaret
Maxwell, E. Jane
Duford, David A.
Salin, E. D.
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H3A 2K6, Canada
[2] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z3, Canada
关键词
D O I
10.1021/ac061616v
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An online standard additions calibration method for transient signals in ICPMS is demonstrated in which a small volume of standard is injected as a spike into the sample/carrier stream, overlaying the analyte peak. This technique provides the advantages of conventional standard additions but requires only a single sample run. The method corrects for matrix effects and is suitable for transient signals in which the severity of the matrix effect changes over the analyte peak. The method uses a peak-fitting program to determine the area of the underlying peak and is shown to be effective for the determination of trace metal concentrations in both a high ionic strength matrix and in a biological matrix (urine). Eight analytes with concentrations in the range of 0.82-233.2 mu g L-1 in urine were simultaneously determined using a standard spiking solution of 75 mu g L-1 injected through a 100-mu L loop. The measured concentrations for analytes free of spectral interferences agreed with the certified values, and the precision achieved was comparable to that achieved by the certifying agency. Using a conventional cross-flow nebulizer and Scott-type spray chamber, the accuracy obtained for online standard additions calibration was within 2%, and the precision was within 5%.
引用
收藏
页码:688 / 694
页数:7
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