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Validation of method for determination of different classes of pesticides in aqueous samples by dispersive liquid-liquid microextraction with liquid chromatography-tandem mass spectrometric detection

机译:液相色谱-串联质谱检测分散液-液微萃取测定水样中不同种类农药的方法的验证

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摘要

In this study, a simple, rapid and efficient method has been developed for the extraction and preconcen-tration of different classes of pesticides, carbofuran (insecticide), clomazone (herbicide) and tebuconazole (fungicide) in aqueous samples by dispersive liquid-liquid microextraction (DLLME) coupled with liquid chromatography-tandem mass spectrometric detection. Some experimental parameters that influence the extraction efficiency, such as the type and volume of the disperser solvents and extraction solvents, extraction time, speed of centrifugation, pH and addition of salt were examined and optimized. Under the optimum conditions, the recoveries of pesticides in water at spiking levels between 0.02 and 2.0μgL~(-1) ranged from 62.7% to 120.0%. The relative standard deviations varied between 1.9% and 9.1% (n = 3). The limits of quantification of the method considering a 50-fold preconcentration step were 0.02 μg L~(-1). The linearity of the method ranged from 1.0 to 1000μgL~(-1) for all compounds, with correlation coefficients varying from 0.9982 to 0.9992. Results show that the method we propose can meet the requirements for the determination of pesticides in water samples. The comparison of this method with solid-phase extraction indicates that DLLME is a simple, fast, and low-cost method for the determination of pesticides in natural waters.
机译:在这项研究中,开发了一种简单,快速,高效的方法,通过分散液-液微萃取对水性样品中的不同种类的农药,呋喃呋喃(杀虫剂),克霉唑(除草剂)和戊唑醇(杀菌剂)进行提取和预富集。 (DLLME)结合液相色谱-串联质谱检测。检查并优化了一些影响萃取效率的实验参数,例如分散剂溶剂和萃取溶剂的类型和体积,萃取时间,离心速度,pH和添加盐的量。在最佳条件下,加标浓度在0.02〜2.0μgL〜(-1)之间的水中农药的回收率为62.7%〜120.0%。相对标准偏差在1.9%和9.1%之间变化(n = 3)。考虑到50倍预浓缩步骤的方法的定量限为0.02μgL〜(-1)。该方法对所有化合物的线性范围为1.0〜1000μgL〜(-1),相关系数为0.9982〜0.9992。结果表明,所提出的方法可以满足水样中农药残留的测定要求。该方法与固相萃取的比较表明,DLLME是测定自然水中农药的一种简单,快速且低成本的方法。

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