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Capillary electrochromatography. Abnormally high efficiencies for neutral-anionic compounds under reversed-phase conditions

机译:毛细管电色谱。反相条件下中性阴离子化合物的异常高效率

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Unusually high efficiencies (up to 2.5 million plates m(-1)) during the capillary electrochromatographic analysis of partially ionized anionic-neutral compounds have been observed under reversed-phase conditions using a standard C-18 stationary phase. An explanation has been proposed in terms of nonequilibrium conditions caused by pulses of stronger or weaker solvent that arise from the sample. The increased efficiencies are observed when the migration time of the analyte is closely matched to the elution time of sample-induced discontinuities in the mobile phase. Repeatability and hence the feasibility to control the system have been demonstrated along with the effect that separation parameters such as mobile-phase organic solvent content, ionic strength, and separation voltage have on peak efficiencies, areas, heights, and asymmetry. Van Deemter plots show that the B term (axial molecular diffusion) is the only major contributor to peak dispersion. A reduced plate height of 0.1 was obtained. The implications of this phenomenon and its ability to cause concurrent electrophoretic effects during the analysis of charged species, thus leading to even greater efficiencies, are discussed. [References: 24]
机译:使用标准C-18固定相在反相条件下已观察到部分电离的阴离子中性化合物的毛细管电色谱分析过程中异常高的效率(高达250万板m(-1))。对于由样品引起的强或弱溶剂脉冲引起的非平衡条件,提出了一种解释。当分析物的迁移时间与流动相中样品诱导的不连续性的洗脱时间紧密匹配时,观察到效率提高。已经证明了可重复性以及控制该系统的可行性,以及分离参数(如流动相有机溶剂含量,离子强度和分离电压)对峰效率,面积,高度和不对称性的影响。 Van Deemter曲线表明,B项(轴向分子扩散)是造成峰色散的唯一主要因素。减小的板高度为0.1。讨论了这种现象的含义及其在带电物质分析过程中引起并发电泳效应的能力,从而提高了效率。 [参考:24]

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