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采用中空纤维保护的液相微萃取结合原位衍生化,随后进行气相色谱 - 质谱联用测定水中化学战剂的降解产物。

Determination of degradation products of chemical warfare agents in water using hollow fibre-protected liquid-phase microextraction with in-situ derivatisation followed by gas chromatography-mass spectrometry.

作者信息

Lee Hoi Sim Nancy, Sng Mui Tiang, Basheer Chanbasha, Lee Hian Kee

机构信息

DSO National Laboratories, 20 Science Park Drive, Singapore 118230, Singapore.

出版信息

J Chromatogr A. 2007 Apr 27;1148(1):8-15. doi: 10.1016/j.chroma.2007.02.104. Epub 2007 Mar 7.

Abstract

Hollow fibre-protected liquid-phase microextraction (HF-LPME) together with gas chromatography/mass spectrometry was investigated for the analysis of degradation products of chemical warfare agents in water samples. The degradation products studied were those of nerve and blister agents, and a psychotomimetic agent. Extractions were successfully performed coupled with in-situ derivatisation using a mixture of solvent and derivatising agent. The protection of the moisture-sensitive derivatising agent was afforded by the hollow fibre. Parameters such as extraction solvent, pH, salt concentration, stirring speed and extraction time were optimised using spiked deionised water samples. The linear range established was between 0.005 and 5 microg ml(-1) depending on analyte, with squared regression coefficients ranging from 0.9929 to 1.0000. Relative standard deviations ranged from 9% to 22%. As compared to those of solid-phase microextraction, the limits of detection (0.01-0.54 microg l(-1)) of the newly-developed approach were significantly improved.

摘要

采用中空纤维保护的液相微萃取(HF-LPME)结合气相色谱/质谱法,对水样中化学战剂的降解产物进行了分析。所研究的降解产物包括神经性毒剂、糜烂性毒剂和一种拟精神病药物的降解产物。使用溶剂和衍生剂的混合物成功进行了萃取,并结合原位衍生化。中空纤维为对湿度敏感的衍生剂提供了保护。使用加标的去离子水样品优化了萃取溶剂、pH值、盐浓度、搅拌速度和萃取时间等参数。根据分析物的不同,建立的线性范围在0.005至5μg ml⁻¹之间,平方回归系数在0.9929至1.0000之间。相对标准偏差在9%至22%之间。与固相微萃取相比,新开发方法的检测限(0.01 - 0.54μg l⁻¹)有显著提高。

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