In situ determination of nerve agents in various matrices by portable capillary electropherograph with contactless conductivity detection

被引:56
作者
Kuban, Petr [1 ]
Seiman, Andrus [1 ]
Makarotseva, Natalja [1 ]
Vaher, Merike [1 ]
Kaljurand, Mihkel [1 ]
机构
[1] Tallinn Univ Technol, Dept Chem, EE-12618 Tallinn, Estonia
关键词
Capillary electrophoresis; Capacitively coupled conductivity detection; Genuine nerve agents; Aqueous extraction; CHEMICAL WARFARE AGENTS; MICELLAR ELECTROKINETIC CHROMATOGRAPHY; INDUCED FLUORESCENCE DETECTION; FLAME PHOTOMETRIC DETECTION; AMPLIFIED SAMPLE STACKING; DEGRADATION-PRODUCTS; ALKYLPHOSPHONIC ACIDS; LIQUID-CHROMATOGRAPHY; METHYLPHOSPHONIC ACID; ELECTROOSMOTIC FLOW;
D O I
10.1016/j.chroma.2011.03.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rapid, efficient and robust methods for sampling and extracting genuine nerve agents sarin, soman and VX were developed for analyzing these compounds on various solid matrices, such as concrete, tile, soil and vegetation. A portable capillary electrophoretic (CE) system with contactless conductometric detection was used for the in situ analysis of the extracted samples. A 7.5 mM MES/HIS-based separation electrolyte accomplished the analysis of target analytes in less than 5 min. The overall duration of the process including instrument start-up, sample extraction and analysis was less than 10 min, which is the fastest screening of nerve agents achieved with liquid phase separation methods to date. The procedure can easily be performed by a person in a protective suit and is therefore suitable for real-life applications. The CE results were validated by an independent GC-MS method and a satisfactory correlation was obtained. The use of a proper sampling strategy with two internal standards and "smart" data-processing software can overcome the low reproducibility of CE. This has a significant impact on the potential acceptance of portable CE instrumentation for the detection and analysis of genuine chemical warfare agents (CWA). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2618 / 2625
页数:8
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