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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >In situ metathesis reaction combined with liquid-phase microextraction based on the solidification of sedimentary ionic liquids for the determination of pyrethroid insecticides in water samples
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In situ metathesis reaction combined with liquid-phase microextraction based on the solidification of sedimentary ionic liquids for the determination of pyrethroid insecticides in water samples

机译:基于沉淀离子液体凝固的原位复分解反应与液相微萃取相结合测定水样中拟除虫菊酯类杀虫剂

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摘要

A novel dispersion liquid-liquid microextraction method based on the solidification of sedimentary ionic liquids (SSIL-DLLME), in which an in situ metathesis reaction forms an ionic liquid (IL) extraction phase, was developed to determine four pyrethroid insecticides (i.e., permethrin, cyhalothrin, fenpropathrin, and transfluthrin) in water followed by separation using high-performance liquid chromatography. In the developed method, in situ DLLME was used to enhance the extraction efficiency and yield. After centrifugation, the extraction solvent, tributyldodecylphosphonium hexafluorophosphate ([P-44412][PF6]), was easily collected by solidification in the bottom of the tube. The effects of various experimental parameters, the quantity of tributyldodecylphosphonium bromide ([P-44412]Br), the molar ratio of [P-44412] Br to potassium hexafluorophosphate (KPF6), the ionic strength, the temperature of the sample solution, and the centrifugation time, were optimized using a Plackett-Burman design to identify the significant factors that affected the extraction efficiency. These significant factors were then optimized using a central composite design. Under the optimized conditions, the recoveries of the four pyrethroid insecticides at four spiked levels ranged from 87.1% to 101.7%, with relative standard deviations (RSDs) ranging from 0.1% to 5.5%. At concentration levels between 1 and 500 mu g/L, good linearity was obtained, with coefficients of determination greater than 0.9995. The limits of detection (LODs) for the four pyrethroid insecticides were in the range of 0.71-1.54 mu g/L. The developed method was then successfully used for the determination of pyrethroid insecticides in environmental samples. (C) 2015 Elsevier B.V. All rights reserved.
机译:开发了一种基于沉淀离子液体凝固的新型分散液-液微萃取方法(SSIL-DLLME),其中原位复分解反应形成离子液体(IL)萃取相,从而确定了四种拟除虫菊酯类杀虫剂(氯菊酯) ,氯氟氰菊酯,联苯丙菊酯和氟氟氰菊酯)在水中,然后使用高效液相色谱进行分离。在开发的方法中,原位DLLME用于提高提取效率和产量。离心后,萃取溶剂六氟磷酸三丁基十二烷基phosph([P-44412] [PF6])易于通过在管底部固化而收集。各种实验参数,三丁基十二烷基溴化(的量([P-44412] Br),[P-44412] Br与六氟磷酸钾(KPF6)的摩尔比,离子强度,样品溶液的温度和使用Plackett-Burman设计优化了离心时间,以确定影响萃取效率的重要因素。然后使用中央复合设计优化这些重要因素。在优化的条件下,四种加标农药含量的四种拟除虫菊酯类农药的回收率在87.1%至101.7%之间,相对标准偏差(RSD)在0.1%至5.5%之间。在1至500μg / L的浓度水平下,可获得良好的线性,测定系数大于0.9995。四种拟除虫菊酯类杀虫剂的检出限在0.71-1.54μg / L范围内。该方法成功用于环境样品中拟除虫菊酯类农药的测定。 (C)2015 Elsevier B.V.保留所有权利。

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