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基于中空纤维的液相微萃取技术结合气相色谱-质谱法测定水样中的拟除虫菊酯类杀虫剂。

Hollow fibre-based liquid-phase microextraction technique combined with gas chromatography-mass spectrometry for the determination of pyrethroid insecticides in water samples.

机构信息

Analytical Chemistry Department, Faculty of Science and Technology, Spain.

出版信息

Talanta. 2012 Oct 15;100:246-53. doi: 10.1016/j.talanta.2012.04.039. Epub 2012 May 15.

Abstract

A simple, easy-to-use, efficient and environmentally friendly method has been developed for the simultaneous analysis of nine pirethroid pesticides in water samples by the combination of hollow fibre-based liquid-phase microextraction (HF-LPME) and gas chromatography-mass spectrometry (GC/MS). For the developed method, nine pirethroid pesticides (esbiothrin, prallethrin, bifenthrin, tetramethrin, phenothrin, permethrin, cyfluthrin, cypermethrin and deltamethrin) were concentrated and well separated under optimal conditions. Several factors that influence the efficiency of HF-LPME were investigated and optimized by means of experimental design. The proposed method has good linearity in the concentration range of 10-400 μg L(-1) with correlation coefficients between 0.995 and 0.999. Overall enrichment factors for the optimized method ranged from 139 to 255 times except for cypermethrin and deltamethrin which ranged from 35 to 128. Detection and quantitation limits of the chromatographic method were in the range of 0.002-0.012 μg L(-1) and 0.003-0.026 μg L(-1) respectively, with RSD values between 4.2% and 18.4%. The recoveries varied in the range of 69.4%-122.7% except for cypermethrin and deltamethrin (17.5%-64.1%) with relative standard deviations between 1.0% and 24.0% for intra and inter-day experiments at different concentrations (0.1 μg L(-1), 0.5 μg L(-1), 1 μg L(-1)). The HF-LPME method optimized was applied to the analysis of three spiked real water samples with good results.

摘要

已经开发出一种简单、易用、高效且环保的方法,通过中空纤维液相微萃取(HF-LPME)和气相色谱-质谱联用(GC/MS)同时分析水样中的九种拟除虫菊酯农药。在开发的方法中,在最佳条件下浓缩并很好地分离了九种拟除虫菊酯农药(烯丙菊酯、炔丙菊酯、溴氰菊酯、四氟菊酯、苯醚菊酯、氯菊酯、氯氟氰菊酯、氯氰菊酯和溴氰菊酯)。通过实验设计研究并优化了影响 HF-LPME 效率的几个因素。所提出的方法在 10-400 μg L(-1) 的浓度范围内具有良好的线性关系,相关系数在 0.995 到 0.999 之间。优化方法的总体富集因子范围为 139 至 255 倍,除氯氟氰菊酯和溴氰菊酯外,范围为 35 至 128 倍。色谱方法的检测限和定量限范围分别为 0.002-0.012 μg L(-1) 和 0.003-0.026 μg L(-1),RSD 值在 4.2%-18.4%之间。回收率范围为 69.4%-122.7%,除氯氟氰菊酯和溴氰菊酯外(17.5%-64.1%),日内和日间实验的相对标准偏差在 1.0%-24.0%之间,浓度不同(0.1 μg L(-1)、0.5 μg L(-1)、1 μg L(-1))。优化后的 HF-LPME 方法应用于分析三个加标实际水样,结果良好。

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