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通过膜乳化辅助液-液微萃取结合漂浮有机液滴固化法测定水样中的四种拟除虫菊酯类杀虫剂。

Determination of four pyrethroid insecticides in water samples through membrane emulsification-assisted liquid-liquid microextraction based on solidification of floating organic droplets.

机构信息

Department of Applied Chemistry, China Agricultural University, Yuanmingyuan West Road 2#, Haidian District, Beijing 100194, China.

Department of Applied Chemistry, China Agricultural University, Yuanmingyuan West Road 2#, Haidian District, Beijing 100194, China.

出版信息

J Chromatogr A. 2018 Jul 20;1559:86-94. doi: 10.1016/j.chroma.2018.04.031. Epub 2018 Apr 13.

Abstract

A novel membrane emulsification-assisted liquid-liquid microextraction method based on the solidification of floating organic drops was used to detect four pyrethroid pesticides (deltamethrin, etofenprox, fenpropathrin, and bifenthrin). In this method, [P]Br was used as a surfactant that could be removed from water via the addition of KPF. The extraction solvent was separated after centrifugation and solidification on the water surface. The parameters affecting the recovery of the target compounds, including the surfactant amount, [P]Br-to-KPF molar ratio, addition of salt, extraction solvent volume, and temperature, were individually optimized and further analyzed through an orthogonal array design (OAD) experiment. The optimized conditions were based on the results of the OAD experiment and single-factor analysis. Using these experimental conditions, the recovery of the four pyrethroids ranged from 91.3% to 98.1% with relative standard deviation (RSD) values ranging from 1.7 to 2.2%. Good linearity was observed, with values from 0.9982 to 0.9997, and the linear range was between 1 and 500 μg/L (5-500 μg/L for fenpropathrin). The limit of detection (LOD) values based on a signal-to-noise ratio (S/N) of 3:1 were 0.37-0.75 μg/L. The enrichment factor ranged from 90 to 96. Therefore, this method is suitable for the determination of pyrethroid pesticides in environmental water samples.

摘要

一种基于悬浮液滴固化的新型膜乳化辅助液液微萃取方法,用于检测四种拟除虫菊酯农药(溴氰菊酯、乙氰菊酯、氯菊酯和联苯菊酯)。在该方法中,[P]Br 用作表面活性剂,通过添加 KPF 可以将其从水中去除。萃取溶剂在离心和在水面上固化后被分离。单独优化了影响目标化合物回收率的参数,包括表面活性剂用量、[P]Br 与 KPF 的摩尔比、加盐量、萃取溶剂体积和温度,并通过正交数组设计(OAD)实验进一步分析。优化条件基于 OAD 实验和单因素分析的结果。使用这些实验条件,四种拟除虫菊酯的回收率在 91.3%至 98.1%之间,相对标准偏差(RSD)值在 1.7%至 2.2%之间。观察到良好的线性关系,值在 0.9982 至 0.9997 之间,线性范围在 1 至 500μg/L(5-500μg/L 用于氯菊酯)之间。基于信噪比(S/N)为 3:1 的检测限(LOD)值为 0.37-0.75μg/L。富集因子范围为 90 至 96。因此,该方法适用于环境水样中拟除虫菊酯农药的测定。

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