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开发一种气相色谱-质谱法,用于测定大气中气相和颗粒相中的农药。

Development of a gas chromatography-mass spectrometry method for the determination of pesticides in gaseous and particulate phases in the atmosphere.

机构信息

Instituto Universitario Centro de Estudios Ambientales del Mediterráneo CEAM-UMH (Fundación CEAM-UMH), Valencia, Spain.

出版信息

Anal Chim Acta. 2011 Aug 5;699(1):57-65. doi: 10.1016/j.aca.2011.05.009. Epub 2011 May 14.

Abstract

A reliable multi-residue method for determining gaseous and particulate phase pesticides in atmospheric samples has been developed. This method, based on full scan gas chromatography-mass spectrometry (GC-MS), allowed the proper determination of sixteen relevant pesticides, in a wide range of concentrations and without the influence of interferences. The pesticides were benfluralin, bitertanol, buprofezin, chlorfenvinphos, chlorpyrifos, chlorpyrifos-methyl, ethalfluralin, fenthion, lindane, malathion, methidathion, propachlor, propanil, pyriproxifen, tebuconazol and trifluralin. Comparisons of two types of sampling filters (quartz and glass fibre) and four types of solid-phase cartridges (XAD-2, XAD-4, Florisil and Orbo-49P) showed that the most suitable supports were glass fibre filter for particulate pesticides and XAD-2 and XAD-4 cartridges for gaseous pesticides (>95% recovery). Evaluations of elution solvents for ultrasonic-assisted extraction demonstrated that isooctane is better than ethylacetate, dichloromethane, methanol or a mixture of acetone:hexane (1:1). Recovery assays and the standard addition method were performed to validate the proposed methodology. Moreover, large simulator chamber experiments allowed the best study of the gas-particle partitioning of pesticides for testing the sampling efficiency for the validation of an analytical multiresidue method for pesticides in air. Satisfactory analytical parameters were obtained, with a repeatability of 5±1%, a reproducibility of 13±3% and detection limits of 0.05-0.18 pg m(-3) for the particulate phase and 26-88 pg m(-3) for the gaseous phase. Finally, the methodology was successfully applied to rural and agricultural samples in the Mediterranean area.

摘要

已经开发出一种可靠的多残留方法,用于测定大气样品中的气态和颗粒相农药。该方法基于全扫描气相色谱-质谱(GC-MS),允许在广泛的浓度范围内,不受干扰的情况下,适当测定十六种相关农药。这些农药包括苯霜灵、丁托特罗、噻嗪酮、氯芬磷、毒死蜱、毒死蜱-甲基、乙呋草黄、硫丹、林丹、马拉硫磷、甲拌磷、丙草胺、丙草胺、吡虫啉、戊唑醇和氟乐灵。两种类型的采样滤器(石英和玻璃纤维)和四种类型的固相萃取小柱(XAD-2、XAD-4、Florisil 和 Orbo-49P)的比较表明,最适合的支持物是用于颗粒状农药的玻璃纤维滤器和用于气态农药的 XAD-2 和 XAD-4 小柱(>95%的回收率)。超声辅助提取洗脱溶剂的评估表明,异辛烷优于乙酸乙酯、二氯甲烷、甲醇或丙酮:己烷(1:1)混合物。回收试验和标准添加法用于验证所提出的方法。此外,大型模拟器室实验允许对农药的气-粒分配进行最佳研究,以测试采样效率,从而验证空气中农药的多残留分析方法的有效性。获得了令人满意的分析参数,颗粒相的重复性为 5±1%,再现性为 13±3%,检测限为 0.05-0.18 pg m(-3),气态相的检测限为 26-88 pg m(-3)。最后,该方法成功应用于地中海地区的农村和农业样品。

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