首页 | 本学科首页   官方微博 | 高级检索  
     

阳离子表面活性剂胶束电动毛细管色谱中的假峰现象
引用本文:陈冠华,杨更亮,田益玲,陈义. 阳离子表面活性剂胶束电动毛细管色谱中的假峰现象[J]. 色谱, 2003, 21(1): 17-19
作者姓名:陈冠华  杨更亮  田益玲  陈义
作者单位:1. 河北大学化学与环境科学学院,河北,保定,071002;河北农业大学生命科学学院,河北,保定,071001
2. 河北大学化学与环境科学学院,河北,保定,071002;中国科学院化学研究所分子科学中心,北京,100080
3. 河北农业大学生命科学学院,河北,保定,071001
4. 中国科学院化学研究所分子科学中心,北京,100080
基金项目:SupportedbothbytheNationalNaturalScienceFoundationofChina (GrantNo . 2 0 0 75 0 0 5 )andtheNaturalScienceFoundationofHebeiProvince,China (GrantNo .2 0 0 0 77,2 0 2 0 96) .
摘    要:研究了以十六烷基三甲基溴化铵为准固定相的胶束电动毛细管色谱中假峰的起源。指出在一定条件下,一个组分可能出现两个峰。实验表明,被分析物双峰的相对峰面积取决于被分析物与表面活性剂反应的时间、温度以及表面活性剂在样品中的浓度。这意味着被分析物与表面活性剂之间的反应是一个慢过程,这种相互作用能够产生一种稳定的物质,并导致假峰的形成。根据实验结果,溶质与胶束之间的快速相互作用机理应被质疑。

关 键 词:假峰  胶束电动毛细管色谱  阳离子表面活性剂  

Pseudo Peak Phenomena in Micellar Electrokinetic Capillary Chromatography by Using Cationic Surfactant
Abstract. Pseudo Peak Phenomena in Micellar Electrokinetic Capillary Chromatography by Using Cationic Surfactant[J]. Chinese journal of chromatography, 2003, 21(1): 17-19
Authors:Abstract
Abstract:Using cetyltrimethylammonium bromide as pseudo stationary phase, the origin of pseudo peak in micellar electrokinetic capillary chromatography was investigated, relating to the fact that under certain conditions two peaks might come arise from a single component. Experiments further showed that the relative areas of the two peaks of an analyte were dependent on the reation time and temperature, under which reactions between analyte and surfactant occurred, and also dependent on concentration of surfactant in sample solutions. The results suggested that the interaction between analyte and surfactant is a slow process, and a stable substance might be formed via the interaction and lead to the formation of pseudo peaks. The fast interaction mechanism between the solute and the micelle could be queried according to the experimental results.
Keywords:cationic surfactant  micellar electrokinetic capillary chromatography  pseudo peak  
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《色谱》浏览原始摘要信息
点击此处可从《色谱》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号