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Development and Validation of GC-ECD Method for the Determination of Metamitron in Soil

机译:GC-ECD法测定土壤中间质子的方法开发与验证

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摘要

This paper aims at developing and validating a convenient, rapid, and sensitive method for estimation of metamitron from soil samples.Determination andquantification was carried out by Gas Chromatography on microcapillary column with an Electron Capture Detector source. The compound was extracted from soil using methanol and cleanup by C-18 SPE. After optimization, the method was validated by evaluating the analytical curves, linearity, limits of detection, and quantification, precision (repeatability and intermediate precision), and accuracy (recovery). Recovery values ranged from 89 to 93.5% within 0.05- 2.0 µg L−1 with average RSD 1.80%. The precision (repeatability) ranged from 1.7034 to 1.9144% and intermediate precision from 1.5685 to 2.1323%. Retention time was 6.3 minutes, and minimum detectable and quantifiable limits were 0.02 ng mL−1 and 0.05 ng g−1, respectively. Good linearity (R 2 = 0.998) of the calibration curves was obtained over the range from 0.05 to 2.0 µg L−1. Results indicated that the developed method is rapid and easy to perform, making it applicable for analysis in large pesticide monitoring programmes.
机译:本文旨在开发和验证一种方便,快速,灵敏的方法来从土壤样品中估算甲胺磷。气相色谱法在带有电子捕获检测器源的微毛细管柱上进行测定和定量。使用甲醇从土壤中萃取该化合物,并通过C-18 SPE进行净化。优化后,通过评估分析曲线,线性,检测限和定量,精度(重复性和中间精度)和准确性(回收率)来验证该方法。回收率在0.05-2.0μgupL -1 范围内,从89%到93.5%,平均RSD为1.80%。精度(重复性)为1.7034至1.9144%,中间精度为1.5685至2.1323%。保留时间为6.3分钟,最低可检测和可量化极限分别为0.02 ngmL -1 和0.05 ng g -1 。在0.05至2.0μgL -1 的范围内,获得了良好的线性曲线(R 2 = 0.998)。结果表明,所开发的方法快速且易于执行,使其适用于大型农药监测计划中的分析。

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