ENVIRONMENTAL ANALYSIS BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY

被引:37
|
作者
Beauchemin, Diane [1 ]
机构
[1] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
inductively coupled plasma mass spectrometry; environmental analysis; natural waters; soils; sediments; vegetation; BIOLOGICAL REFERENCE MATERIALS; ISOTOPE RATIO MEASUREMENTS; SOLID-PHASE MICROEXTRACTION; DYNAMIC-REACTION-CELL; RARE-EARTH-ELEMENTS; DIRECT SAMPLE INSERTION; HEATING-ELECTROTHERMAL VAPORIZATION; PERFORMANCE LIQUID-CHROMATOGRAPHY; ANION-EXCHANGE CHROMATOGRAPHY; ULTRA-TRACE DETERMINATION;
D O I
10.1002/mas.20257
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
This article reviews the numerous ways in which inductively coupled plasma mass spectrometry has been used for the analysis of environmental samples since it was commercially introduced in 1983. Its multielemental isotopic capability, high sensitivity and wide linear dynamic range makes it ideally suited for environmental analysis. Provided that some care is taken during sample preparation and that appropriate calibration strategies are used to circumvent non-spectroscopic interferences, the technique is readily applicable to the analysis of a wide variety of environmental samples (natural waters, soils, rocks, sediments, vegetation, etc.), using quadrupole, time-of-flight or double-focusing sector-field mass spectrometers. In cases where spectroscopic interferences arising from the sample matrix cannot be resolved, then separation methods can be implemented either on- or off-line, which can simultaneously allow analyte preconcentration, thus further decreasing the already low detection limits that are achievable. In most cases, the blank, prepared by following the same steps as for the sample but without the sample, limits the ultimate detection limits that can be reached. (C) 2009 Wiley Periodicals, Inc., Mass Spec Rev 29:560-592, 2010
引用
收藏
页码:560 / 592
页数:33
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