The stacking boundary in capillary electrophoresis

被引:0
|
作者
Quirino, JP [1 ]
Terabe, S [1 ]
机构
[1] Himeji Inst Technol, Fac Sci, Kamigori, Hyogo 6781297, Japan
关键词
sample stacking; stacking boundary; vacancy and differential capillary electrophoresis; capillary zone electrophoresis; micellar electrokinetic chromatography;
D O I
10.1002/(SICI)1520-667X(1999)11:7<513::AID-MCS3>3.0.CO;2-L
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The stacking boundary (SB) in capillary electrophoresis (CE) is elucidated. The SE is different from the electrolyte boundaries; for example, the composition of the SE changes with time while the composition of the electrolyte boundaries ideally does not change with time. All these boundaries originate from an original concentration boundary found between the sample solution and background solution zones before application of voltage. The differences in electrophoretic mobilities cause them to separate from each other, as verified from the enhanced field Vacancy CE experiments and a special experiment. Theoretical and some experimental studies on the fate of analyte zones in vacancy and differential CE are presented. Some equations are derived that provide insight into the behavior of analyte zones in enhanced field vacancy CE. Furthermore, it was found that the composition and especially the conductivity of the sample solution in vacancy and differential CE experiments are crucial in maintaining reproducibility of data and reliability for qualitative and quantitative analysis. (C) 1999 John Wiley & Sons, Inc.
引用
收藏
页码:513 / 520
页数:8
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