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首页> 外文期刊>Analytical methods >Surfactant-less water emulsion based dispersive liquid–liquid microextraction for determination of organophosphorus pesticides in aqueous samples
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Surfactant-less water emulsion based dispersive liquid–liquid microextraction for determination of organophosphorus pesticides in aqueous samples

机译:基于无表面活性剂的水乳液分散液-液微萃取法测定水性样品中的有机磷农药

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摘要

A new sample preparation method, surfactant-less water emulsion based dispersive liquida€“liquid microextraction coupled with gas chromatography-flame ionization detection, has been developed for the extraction, preconcentration and determination of some organophosphorus pesticides including diazinon, malathion, chlorpyrifos, profenofos, and phosalone from aqueous samples. In the present method an extraction solvent is dispersed into de-ionized water by repeated suction and injection of the extraction solvent and de-ionized water mixture using a syringe. This leads to formation of a water-based emulsion of the extraction solvent. Then this emulsion is rapidly injected into an aqueous sample solution containing the target analytes. Fine organic phase droplets are dispersed in all parts of the aqueous phase. Indeed de-ionized water acts as a disperser. After extraction, phase separation is performed by centrifugation and the enriched analytes in the sedimented phase are determined by the chromatographic system. Under the optimum extraction conditions, the method showed low limits of detection and quantification between 0.65a€“4.2 and 1.9a€“13 ng mLa?’1, respectively. Enrichment factors and extraction recoveries were in the ranges of 1280a€“1620 and 64a€“81%, respectively. Relative standard deviations for the extraction of 15 ng mLa?’1 of each pesticide were less than 8.4% for intra-day (n = 6) and inter-day (n = 4) precisions. Finally some juice samples were successfully analyzed using the proposed method and two analytes, diazinon and phosalone, were determined in some of them at the ng mLa?’1 level.
机译:已经开发了一种新的样品前处理方法,即基于无表面活性剂的水乳液型分散微液体结合气相色谱-火焰电离检测技术,用于萃取,预浓缩和测定一些有机磷农药,包括二嗪农,马拉硫磷,毒死rif,丙溴磷,和水性样品中的去草甘膦。在本方法中,通过使用注射器重复抽吸和注入萃取溶剂和去离子水混合物,将萃取溶剂分散到去离子水中。这导致形成萃取溶剂的水基乳液。然后将该乳液快速注入含有目标分析物的样品水溶液中。精细的有机相液滴分散在水相的所有部分中。实际上,去离子水可以起到分散剂的作用。提取后,通过离心进行相分离,并通过色谱系统确定沉淀相中富集的分析物。在最佳提取条件下,该方法的检出限和定量限分别在0.65a?4.2和1.9a?13 ng mLa?-1之间。富集因子和提取回收率分别在1280a·1620和64a·81%的范围内。对于日内(n = 6)和日间(n = 4)精度,提取15 ng mLa?1的每种农药的相对标准偏差小于8.4%。最后,使用所提出的方法成功地分析了一些果汁样品,并在其中的ng mLa?’1水平中确定了其中的两种分析物,二嗪农和phosalone。

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