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作 者:李继民[1] 王彦吉[2] 赵彦军[1] 邹宁[1]
机构地区:[1]中国刑警学院法医系,沈阳110035 [2]中国人民公安大学,北京100038
出 处:《理化检验(化学分册)》2010年第9期1052-1054,共3页Physical Testing and Chemical Analysis(Part B:Chemical Analysis)
基 金:国家高技术产业发展项目(No.20012492)资助
摘 要:采用气相色谱法对离子液体中间体中N-甲基咪唑残留量进行测定。以N,N-二甲基苯胺作为内标,采用DB-FFAP石英毛细管色谱柱(30 m×0.32 mm,0.25μm)分离,用氮磷检测器测定。N-甲基咪唑的质量浓度在0.02-0.140 g.L-1范围内与其峰面积呈线性关系,检出限(3S/N)为6.52 mg·L^-1,测定下限(10S/N)为21.73 mg·L^-1。在两个浓度水平作回收试验,平均回收率(n=5)分别为96.4%,96.2%,测定结果的相对标准偏差(n=5)为0.88%。Residual amount of N-methylimidazole in ionic liquid intermediates was determined by GC with nitrogen-phosphorus detector(NPD).N,N-dimethylaniline was used as internal standard.The sample solution was separated on DB-FFAP capillary column(30 m×0.32 mm,0.25 μm).Linear relationship between values of peak area and mass concentration of N-methylimidazole was obtained in the range of 0.02-0.140 g·L^-1,with values of limit of detection(3S/N) and lower limit of determination(10S/N) of 6.52 mg·L^-1 and 21.73 mg·L^-1,respectively.Test for recovery was made at two concentration levels,giving results of 96.4% and 96.2%.Value of RSD(n=5) found from the analytical results was 0.88%.
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