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作 者:徐宜宏 黄莹滢[2] 于丽 付海滨[2] 张欣媛[2] 张敏[1] XU Yi-hong;HUANG Ying-ying;YU Li;FU Hai-bin;ZHANG Xin-yuan;ZHANG Min(College of Engineering, Shenyang Agricultural University, Shenyang 110866, China;Shenyang Entry-Exit Inspection and Quarantine Bureau, Shenyang 110016, China)
机构地区:[1]沈阳农业大学工程学院,沈阳110866 [2]沈阳出入境检验检疫局,沈阳110016
出 处:《农药》2018年第6期435-437,共3页Agrochemicals
基 金:沈阳市科技计划项目(17-159-8-00);辽宁省大型科学仪器设备共享服务平台能力建设项目(2017-2018年度)
摘 要:[目的]建立毒杀芬在农田土壤中残留量的气相色谱检测方法。[方法]样品采用正己烷提取后,经PSA和Carb净化,气相色谱电子捕获检测器测定,外标法定量。[结果]方法定量限(S/N=10∶1)为0.01 mg/kg,在0.10~3.0 mg/L的质量浓度范围内,相关系数为0.998,在土壤中添加0.01~0.1 mg/kg范围内(n=6),回收率为75%~92%,相对标准偏差(RSD)为4.1%~5.4%。[结论]该方法适用于土壤中毒杀芬的快速检测。[Aims] A method was developed for the determination of toxaphene residues in soil by capillary gas chromatographic. [Methods] The pesticide was extracted using n-hexane and purified by PSA and Carb, finally detected by GC-electron capture detector, external standard method for quantitative. [Results] The limit of quantitation(S/N=10∶1) was 0.01 mg/kg. In the linear range of 0.10-3.0 mg/L, the correlation coefficient was 0.998. In a range of 0.01-0.1 mg/kg(n=6), the corresponding recoveries were 75-92%, the relative standard deviations(RSD) were 4.1-5.4%.[Conclusions] The method is suitable for rapid detection of toxaphene residues in soil.
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