IONIC-STRENGTH AND CHARGE NUMBER CORRECTION FOR MOBILITIES OF MULTIVALENT ORGANIC-ANIONS IN CAPILLARY ELECTROPHORESIS

被引:134
作者
FRIEDL, W
REIJENGA, JC
KENNDLER, E
机构
[1] EINDHOVEN UNIV TECHNOL,DEPT CHEM ENGN,5600 MB EINDHOVEN,NETHERLANDS
[2] UNIV VIENNA,INST ANALYT CHEM,A-1090 VIENNA,AUSTRIA
关键词
D O I
10.1016/0021-9673(95)00159-K
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An empirical expression was derived for the actual mobility, mu, valid in an extended range of ionic strength, I, between 0.001 and 0.1 mol/l, using a three-parameter exponential fit for the ratio of actual and absolute mobilities (mu(0) at I = 0), which consists of two variables: ionic strength of the buffer and charge number, z, of the solute. The charge numbers of the solute anions (21 aromatic sulfonates) ranged between 1 and 6, and the ionic strength was varied in the range mentioned using a sodium acetate buffer. The mobilities were determined at 25.0 degrees C in a coated capillary with suppressed electroosmotic flow. The resulting fitting equation, valid under these conditions, is mu/mu(0) = exp(-0.77 root zI). The difference between measured mobilities and mobilities calculated from a tenfold higher or lower ionic strength, using this equation, is within 5% for all experiments. For multivalent ions, mu values can be derived from mu(0) with comparable accuracy.
引用
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页码:163 / 170
页数:8
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