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作 者:陈春梅 李晴 谢枫彤 肖林平 CHEN Chun-mei;LI Qing;XIE Feng-tong;XIAO Lin-ping(Guangzhou Analytical Center Branch of Technology Development Company in Shantou Branch,Guangdong Shantou 515041;Guangdong Institute of Analysis (China National Analytical Center,Guangzhou),Guangdong Guangzhou 510070,China)
机构地区:[1]广州分析测试中心科力技术开发公司汕头分公司,广东汕头515041 [2]广东省测试分析研究所(中国广州分析测试中心),广东广州510070
出 处:《广州化工》2019年第4期95-97,共3页GuangZhou Chemical Industry
摘 要:介绍了一种气相色谱法测定1-2%毒死蜱药液中毒死蜱含量方法的建立,并从专属性、线性和范围、准确度、精密度、检出限和定量限以及实际样品检测等方面进行了方法学验证。经方法学验证,在毒死蜱及内标邻苯二甲酸二正戊酯出峰位置没有干扰,专属性好;毒死蜱浓度在0. 02~2. 00 mg/m L范围线性相关系数为0. 9995,线性好;回收率101%~102%,准确度高;相对标准偏差0. 58%,精密度高;方法的检出限为0. 00075%,定量限为0. 00255%。The establishment of a method for determination of chlorpyrifos in 1 -2% chlorpyrifos solution by gas chromatography was introduced, and the methodological verification was carried out from the specificity, linearity and range, accuracy, precision, detection limit and quantitation limit, actual sample test.According to the methodological verification, there was no interference in the peak position of chlorpyrifos and internal standard di-n-pentyl phthalate, and the specificity was good.The linear correlation coefficient of chlorpyrifos concentration in the range of 0.02 ~ 2.00 mg/ mL was 0.9995, and the linearity was good.The recovery rate was 101%~102%, and the accuracy was high. The relative standard deviation was 0.58%, and the precision was high.The detection limit of the method was 0.00075%, and the limit of quantification was 0.00255%.
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