机构地区: 华中农业大学畜牧兽医学院兽药研究所
出 处: 《色谱》 2009年第2期176-180,共5页
摘 要: 建立了一种大豆和玉米中20种农药残留量的分散固相萃取气相色谱-负化学离子源质谱分析方法。样品经乙腈提取并浓缩后加入N-丙基乙二胺(PSA)、石墨化碳黑和C183种填料进行分散固相萃取净化,气相色谱-负化学离子源质谱分时段选择离子监测技术测定与确证,外标法定量。所有农药在20~400μg/L范围内线性均良好;方法的定量限(LOQ)均不高于2μg/kg;在5,10和20μg/kg3个添加水平下所有农药的平均回收率均处于70%~130%之间,相对标准偏差(RSD)低于17%;运用该方法检测大豆和玉米样品时没有干扰现象。 A method was developed for the determination of 20 kinds of pesticide residues in soybeans and corn with the technique of offline disperse solid-phase extraction and gas chromatography-negative chemical ionization mass spectrometry(GC-NCI/MS).The pesticides interested were extracted twice from the samples with acetonitrile.The combined extract was concentrated to dryness and redissolved in acetonitrile,then cleaned up by dispersive solid-phase extraction with sorbents of N-propyl ethylene diamine(PSA),graphited carbon black,and C18,and determined and confirmed by GC-NCI/MS.The recoveries of all pesticides were in the range of 70%-130% at three spiked levels(5,10 and 20 μg/kg),and the relative standard deviations were below than 17%.The linearity of the method was good in the concentration range of 20-400 μg/L,and limits of quantification(LOQs) were no more than 2 μg/kg.The method is selective well with no interference and suitable for the confirmatory of pesticide residues in soybeans and corn.