...
首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Adamantyl-group containing mixed-mode acrylamide-based continuous beds for capillary electrochromatography. Part II. Characterization of the synthesized monoliths by inverse size exclusion chromatography and scanning electron microscopy
【24h】

Adamantyl-group containing mixed-mode acrylamide-based continuous beds for capillary electrochromatography. Part II. Characterization of the synthesized monoliths by inverse size exclusion chromatography and scanning electron microscopy

机译:含金刚烷基的混合模式丙烯酰胺基连续床用于毛细管电色谱。第二部分逆尺寸排阻色谱法和扫描电子显微镜表征合成的整体

获取原文
获取原文并翻译 | 示例
           

摘要

In our previous article we have described the synthesis of a new amphiphilic monolithic stationary phase by in situ free radical copolymerization of cyclodextrin-solubilized N-adamantyl acrylamide, piperazinediacrylamide, methacrylamide and vinylsulfonic acid in aqueous medium in pre-treated fused silica capillaries of 100 μm I.D. In the present work, we study the morphology of different monolithic stationary phases synthesized under variation of the concentration of ammonium sulfate in the polymerization mixture. The pore size distribution is determined with inverse size exclusion chromatography (ISEC) using the retention data of a series of polystyrene standards with narrow molecular size distribution and known average molar mass ranging from 1560 to 2010000gmol~(-1). The impact of the concentration of the lyotropic salt ammonium sulfate in the polymerization mixture on the formed morphology, the pore size distribution, and the fractional volume of mesopores and macropores is determined. The homogeneity and uniformity of the formed monolith over the length of the capillary and the covalent attachment to the confining walls are confirmed. Repetition of the synthesis procedure shows that these morphology parameters are well controlled as there is an excellent capillary-to-capillary, day-to-day, and run-to-run reproducibility reached for the electroosmotic mobility and the retention factor determined with alkylphenones in the reversed-phase mode.
机译:在我们之前的文章中,我们描述了在水性熔融石英毛细管中,在水介质中通过环糊精增溶的N-金刚烷基丙烯酰胺,哌嗪二丙烯酰胺,甲基丙烯酰胺和乙烯基磺酸的原位自由基共聚反应,合成新的两亲整体固定相的方法。 ID在目前的工作中,我们研究了在聚合混合物中硫酸铵浓度变化下合成的不同整体固定相的形貌。孔径分布通过逆尺寸排阻色谱法(ISEC)使用一系列分子量分布窄且已知平均摩尔质量为1560至2010000gmol〜(-1)的聚苯乙烯标样的保留数据确定。确定了聚合混合物中溶致盐硫酸铵的浓度对所形成的形态,孔径分布以及中孔和大孔的分数体积的影响。证实了在毛细管的整个长度上所形成的整料的均质性和均匀性以及共价附接至限制壁。重复合成过程表明,这些形态参数得到了很好的控制,因为电渗迁移率和保留的苯乙酮含量决定了保留时间,在毛细管,毛细管,日常和运行之间均具有出色的重现性。反相模式。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号