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A multi‐component method to determine pesticides in surface water by liquid‐chromatography tandem quadrupole mass spectrometry

机译:液相色谱串联四极杆质谱法测定地表水中农药的多组分方法

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摘要

Pesticide pollution of surface water is a major concern in many agricultural catchments The development of rapid and accurate methods for determining pesticide concentrations in water samples is, therefore, important. Here we describe a method for the simultaneous analysis of six pesticides (metaldehyde, quinmerac, carbetamide, metazachlor, propyzamide and pendimethalin) in natural waters by direct aqueous injection with liquid chromatography-tandem mass spectrometry. The method validation showed good linearity from 0.2 to 50.0 µg/L with correlation coefficients between 0.995 and 0.999. Method accuracy ranged from 84 to 100% and precision Relative standard deviation (RSD) from 4 to 15%. The limits of detection for the targeted pesticides ranged from 0.03 to 0.36 µg/L. No significant matrix effects on quantification were observed (t-test). The method was tested on water samples from a small arable catchment in eastern England. Peak concentrations for the determinands ranged from 1 to 10 µg/L.
机译:在许多农业流域,地表水的农药污染是一个主要问题。因此,开发快速,准确的测定水样中农药浓度的方法非常重要。在这里,我们描述了一种通过液相色谱-串联质谱法直接水样进样同时分析天然水中六种农药(甲醛,喹美拉克,羧甲酰胺,间草胺,丙酰胺和戊二甲灵)的方法。方法验证显示出0.2至50.0 µg / L的良好线性,相关系数在0.995至0.999之间。方法的准确度从84%到100%不等,精确度相对标准偏差(RSD)从4%到15%不等。目标农药的检出限为0.03至0.36 µg / L。没有观察到对定量的显着基质影响(t检验)。该方法在英格兰东部一个小耕地流域的水样上进行了测试。测定的峰值浓度范围为1至10 µg / L。

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