首页> 外文期刊>Journal of Food Composition and Analysis >Determination of pyrethroid pesticides residues in vegetable oils using liquid-liquid extraction and dispersive liquid-liquid microextraction followed by gas chromatography-flame ionization detection.
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Determination of pyrethroid pesticides residues in vegetable oils using liquid-liquid extraction and dispersive liquid-liquid microextraction followed by gas chromatography-flame ionization detection.

机译:液-液萃取-分散液-液微萃取-气相色谱-火焰电离检测法测定植物油中拟除虫菊酯类农药的残留量

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摘要

A simple, fast and economical method has been developed for the determination of fenpropathrin, sumithrin, cyhalothrin, permethrin and deltamethrin in vegetable oils. The method is based on a dispersive liquid-liquid microextraction (DLLME) technique after a preliminary liquid-liquid extraction step, which is followed by a gas chromatography-flame ionization detection or gas chromatography-mass spectrometry determination. Initially oil samples were partitioned in a dimethylformamide (DMF)-hexane mixture and then DMF was removed and used as a disperser solvent in the following DLLME procedure in which muL-level of 1,1,2-trichloroethane was used as an extraction solvent. The detection limits ranged from 0.02 to 0.16 mg kg-1 and the relative standard deviations (RSD %) for four repeated experiments (C = 0.2 and 0.6 mug kg-1 of each pesticide) varied from 2% to 13%, and enrichment factors were in the ranges of 40-70. In p value of 0.9, neither significant matrix effects nor interferences were observed by employing the proposed treatment in analysis of oil samples, and the extraction recoveries obtained for the samples spiked with 0.2, 0.6 and 1.1 mg kg-1 levels varied from 109 +or- 3% to 85 +or- 5%. The method was successfully applied in determination of target analytes in vegetable oils
机译:已开发出一种简单,快速且经济的方法来测定植物油中的苯丙酸菊酯,扑热息痛,氯氟氰菊酯,氯菊酯和溴氰菊酯。该方法基于在初步液-液萃取步骤之后的分散液-液微萃取(DLLME)技术,然后进行气相色谱-火焰电离检测或气相色谱-质谱测定。最初,将油样品分配在二甲基甲酰胺(DMF)-己烷混合物中,然后将DMF除去,并在以下DLLME程序中用作分散溶剂,其中将多分子水平的1,1,2-三氯乙烷用作萃取溶剂。四个重复实验(C = 0.2和0.6杯kg -1 )的检测限范围为0.02至0.16 mg kg -1 和相对标准偏差(RSD%)。每种农药的含量从2%到13%不等,富集系数在40-70范围内。在p值为0.9时,采用建议的处理方法对油样进行分析时,未观察到明显的基质效应和干扰,并且对加标有0.2、0.6和1.1 mg kg -1 水平从109±3%到85±5%。该方法已成功应用于植物油中目标分析物的测定

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