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Capillary liquid chromatography and capillary electrochromatography using silica hydride stationary phases

机译:使用氢化硅固定相的毛细管液相色谱和毛细管电色谱

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摘要

A hydride-based octadecyl stationary phase on both 4.0 and 1.8 mu m silica particles is tested in both the capillary LC and the pressurized capillary electrochromatography (pCEC) modes. These two materials are compared to standard C18 stationary phase made by organosilanization and to the hydride material packed into a convention 4.6 mm I.D. column. The performance of the capillary columns is evaluated in terms of analysis times for various mixtures as well as efficiency. Of particular interest are the differences between the LC mode where only laminar flow is present and pCEC operation where a flat electrodriven flow profile is superimposed on the parabolic pressurized flow. Differences in performance between columns packed with 4.0 and 1.8 mu m particle silica are also evaluated.
机译:在毛细管LC和加压毛细管电色谱(pCEC)模式下都测试了4.0和1.8μm二氧化硅颗粒上基于氢化物的十八烷基固定相。将这两种材料与通过有机硅烷化制成的标准C18固定相以及包装到常规4.6 mm I.D.中的氢化物材料进行比较。柱。根据各种混合物的分析时间和效率评估毛细管柱的性能。特别令人关注的是LC模式(仅存在层流)与pCEC操作之间的差异,在该模式下,平面电驱动流量分布叠加在抛物线增压流量上。还评估了填充有4.0和1.8μm颗粒二氧化硅的色谱柱之间的性能差异。

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