Improvement of the capabilities of inductively coupled plasma optical emission spectrometry by replacing the desolvation system of an ultrasonic nebulization system with a pre-evaporation tube

被引:27
作者
Asfaw, Alemayehu [1 ]
Beauchemin, Diane [1 ]
机构
[1] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
关键词
Ultrasonic nebulizer; Pre-evaporation tube; Desolvation system; ICP-OES; Plasma robustness; MASS SPECTROMETRY; INTERNAL STANDARDIZATION; MATRIX INTERFERENCES; SAMPLE INTRODUCTION; WATER; SOLVENT; MERCURY; ELEMENT; FLOW;
D O I
10.1016/j.sab.2010.03.013
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The effect of replacing the desolvation system (i.e., heater/condenser (HC) and membrane desolvator (MD)) of an ultrasonic nebulizer (USN) system with a pre-evaporation tube (PET) that is heated to about 400 C on the analytical capabilities of inductively coupled plasma optical emission spectrometry (ICP-OES) was investigated. A multivariate optimisation was conducted in each case to find operating conditions maximizing plasma robustness. Under optimum conditions, the analytical performance of ICP-OES was significantly improved (i.e., better sensitivity, detection limit and plasma robustness) with USN-PET compared to that achieved with both the commercially-available USN-HC-MD and a conventional pneumatic nebulizer/spray chamber sample introduction system. However, only the USN-PET approach allows the determination of Hg, which appears to otherwise be lost in the heater/condenser system. Using a simple external calibration, without any matrix matching, and using an argon emission line for internal standardization, the results obtained for the determination of trace elements in certified soil reference materials (SRM 2710 and 2711) by USN-PET were in good agreement with certified values. This is unlike with conventional sample introduction systems where internal standardization using an Ar line is unusual, as it does not compensate for physical interferences, and either internal standardization (with internal standards added to the sample and standard solutions) or matrix-matched calibration is required. (C) 2010 Elsevier BM. All rights reserved.
引用
收藏
页码:376 / 384
页数:9
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