Characterization of the cationic surfactant induced reversal of electroosmotic flow in capillary electrophoresis

被引:172
作者
Lucy, CA
Underhill, RS
机构
[1] Department of Chemistry, University of Calgary, Calgary, Alta., T2N 1N4
关键词
D O I
10.1021/ac950632h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Reversal of electroosmotic now in capillary electrophoresis can be achieved by the addition of cationic surfactants to the electrophoretic buffer. This reversal of now is caused by the formation of a bilayer or hemimicelle at the walls of the capillary, effectively making the wall charge positive, The bilayer can be formed either by adsorption of monomeric surfactants or by admicelles (surfactant pairs), depending on the ionic strength of the buffer and the surface charge at the capillary walls. At concentrations of cationic surfactant sufficient to form the bilayer (i.e., greater than the critical micelle concentration) the electroosmotic now velocity is independent of pH above a pH of 4. Adjustment of the ionic strength causes minor variations in the reversed electroosmotic now rate due to the opposing forces of increased concentration of adsorbed surfactant and decreased double layer thickness. The nature of the anionic counterion in solution has a strong effect on the magnitude of the reversed electroosmotic now observed, analogous to the effect of the buffer cation's effect on normal electroosmotic now. This effect is explained using a simple ion exchange model.
引用
收藏
页码:300 / 305
页数:6
相关论文
共 47 条
[1]   HIGH-VOLTAGE CAPILLARY ZONE ELECTROPHORESIS - OPERATING PARAMETERS EFFECTS ON ELECTROENDOSMOTIC FLOWS AND ELECTROPHORETIC MOBILITIES [J].
ALTRIA, KD ;
SIMPSON, CF .
CHROMATOGRAPHIA, 1987, 24 :527-532
[2]   CHARACTERIZATION OF SILICA SURFACES BY ADSORPTION FROM SOLUTION - INVESTIGATIONS INTO MECHANISM OF ADSORPTION OF CATIONIC SURFACTANTS [J].
BIJSTERBOSCH, BH .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1974, 47 (01) :186-198
[3]   ADSORPTION OF IONIC SURFACTANTS ON CONSTANT CHARGE SURFACES - ANALYSIS BASED ON A SELF-CONSISTENT FIELD LATTICE MODEL [J].
BOHMER, MR ;
KOOPAL, LK .
LANGMUIR, 1992, 8 (06) :1594-1602
[4]   SEPARATION OF SULFONATE AND SULFATE SURFACTANTS BY CAPILLARY ELECTROPHORESIS - EFFECT OF BUFFER CATION [J].
CHEN, SH ;
PIETRZYK, DJ .
ANALYTICAL CHEMISTRY, 1993, 65 (20) :2770-2775
[5]   HEMIMICELLE FORMATION OF CATIONIC SURFACTANTS AT THE SILICA-GEL WATER INTERFACE [J].
GAO, YY ;
DU, JH ;
GU, TR .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1987, 83 :2671-2679
[6]  
GAUDIN AM, 1955, T AM I MIN MET ENG, V202, P958
[7]  
GROSSMAN PD, 1992, CAPILLARY ELECTROPHO, pCH1
[8]  
GROSSMAN PD, 1992, CAPILLARY ELECTROPHO, P118
[9]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY OF ORGANIC-ACIDS WITH POTENTIOMETRIC DETECTION USING A METALLIC COPPER ELECTRODE [J].
HADDAD, PR ;
ALEXANDER, PW ;
TROJANOWICZ, M .
JOURNAL OF CHROMATOGRAPHY, 1984, 315 (DEC) :261-270
[10]  
HADDAD PR, 1990, ION CHROMATOGRAPHY, P89