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毛细管气相色谱法定量测定氮酮
引用本文:孙心齐,刘小强,魏敏,王超杰,赵瑾.毛细管气相色谱法定量测定氮酮[J].化学研究,2003,14(4):60-62.
作者姓名:孙心齐  刘小强  魏敏  王超杰  赵瑾
作者单位:1. 河南大学,化学化工学院,河南,开封,475001
2. 商丘师范学院
基金项目:河南大学重点学科经费资助项目.
摘    要:对毛细管柱定量测定氮酮的操作条件进行了探索 选择了以DB 1型石英毛细管色谱柱φ0.53mm×30m,宽口径进样口不分流进样,FID检测器,压力程序升压,柱温箱程序升温,进样量1μL的色谱条件,对氮酮样品进行检测,各组分分离良好 定量检测结果:线性范围为20μg~0.2μg,线性方程:Y=6.0888×106+1.41573×107X,r=0.99997,,加标回收率为100.25%,仪器精密度RSD=0.45%,满足定量分析的要求

关 键 词:氮酮  定量分析  毛细管气相色谱
文章编号:1008-1011(2003)04-0060-03
修稿时间:2003年6月5日

Capillary Chromatographic Determination of Laurocapram
SUN Xin-qi,LIU Xiao-qiang,WEI Min,WANG Chao-jie,ZHAO Jin.Capillary Chromatographic Determination of Laurocapram[J].Chemical Research,2003,14(4):60-62.
Authors:SUN Xin-qi  LIU Xiao-qiang  WEI Min  WANG Chao-jie  ZHAO Jin
Abstract:The determination method of laurocapram by capillary chromatography was studed. The chromatographic conditions such as DB-1 silicon capillary column (φ0.53 mm×30 m),wide bore injection port , splitless injection, FID detector and the increase of pressure and oven temperature controlled by programs were selected. The results showed that a good separation effect and linear range (20~0.2 μg) were obtained in quantitative determination . The linear equation is Y=6.088 8×10~(6)+1.415 73×10~(7 )X,r=0.999 97. The average recovery is 100.25 % and the instrumental precision is 0.45 %. The requirements of quantitative analysis are met in this experiment.
Keywords:laurocapram  quantitative analysis  capillary chromatography
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