首页> 外文期刊>Journal of AOAC International >Simplified pesticide multiresidue analysis of soybean oil by low-temperature cleanup and dispersive solid-phase extraction coupled with gas chromatography/mass spectrometry
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Simplified pesticide multiresidue analysis of soybean oil by low-temperature cleanup and dispersive solid-phase extraction coupled with gas chromatography/mass spectrometry

机译:通过低温清理和分散固相提取与气相色谱/质谱耦合大豆油的简化杀虫剂多层分析

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摘要

A simple, fast, and economical method has been developed for the simultaneous determination of 28 various types of pesticides in soybean oil. Pesticides of low molecular mass were separated from the fat of the oil, which has a high molecular mass, by using low-temperature fat precipitation, followed by a cleanup process based on dispersive solid-phase extraction with primary secondary amine and C18 as sorbents and magnesium sulfate for the removal of residual water. The results for all pesticides determined by gas chromatography with mass spectrometry in the selected-ion monitoring mode were linear, and the matrix effect of the method was evaluated. Recoveries of most pesticides were acceptable at fortification levels of 0.02, 0.05, 0.2, and 1 mg/kg. The relative standard deviation was <20% even for determinations without internal standards. Limits of quantitation ranged from 20 to 250 microg/kg.
机译:已经开发了一种简单,快速,经济的方法,用于同时测定大豆油中的28种各种类型的农药。 通过使用低温脂肪沉淀,将低分子量的农药与具有高分子质量的油的脂肪分离,然后基于用初级仲胺和C18作为吸附剂的分散固相提取 硫酸镁用于去除残留的水。 通过在所选离子监测模式中与质谱法测定的所有农药的结果是线性的,评价该方法的基质效果。 在502,0.05,0.2和1mg / kg的固化水平下可以接受大多数农药的回收率。 即使没有内部标准的测定,相对标准偏差均匀<20%。 定量限制范围为20至250 microg / kg。

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