ELECTRICALLY CONTROLLED ELECTROFOCUSING OF AMPHOLYTES BETWEEN 2 ZONES OF MODIFIED ELECTROLYTE WITH 2 DIFFERENT VALUES OF PH

被引:66
作者
POSPICHAL, J
DEML, M
BOCEK, P
机构
[1] Institute of Analytical Chemistry, Czech Academy of Sciences, 611 42 Brno
来源
JOURNAL OF CHROMATOGRAPHY | 1993年 / 638卷 / 02期
关键词
D O I
10.1016/0021-9673(93)83426-S
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method is described for the separation and concentration of ampholytes from their mixtures with other ionic species. In a quadrupole electromigration column, two zones of different pHs are created by using controlled flows of the solvolytic ions (H+ and OH-) from appropriate electrode chambers at opposite sides of the column. Thus, a time-variable interface is created between two zones with a sharp change of pH. The position of the interface in the column, the direction and velocity of its movement and the difference in pH across the interface-pH gap can be adjusted by electric currents. This arrested interface is reasonably stable with time and has the following separation properties: ampholytes with pI values between the pHs of both zones are focused into a zone at interface; and other types of ampholytes and other weak or strong ions are not trapped at the interface. The basic properties of the above system are described and experiments showing the effects of the type of sample (ampholyte, weak ion), time, the concentration of primary electrolyte and the additives changing the viscosity, solubility or pI of ampholyte are given. The method proposed offers the following advantages: the ampholytes in the sample may be concentrated several hundred-fold; the focused zones have sharp boundaries (zones 0.1 mm in length were prepared) and high concentrations of the trapped species; the zone of a trapped ampholyte contains the ampholyte proper and simple ions of primary electrolyte (KCl) only; and the zones can be shifted to any selected position in the column (potentially to the location of a detector cell or a collection device).
引用
收藏
页码:179 / 186
页数:8
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