Influence of mobile phase composition on electroosmotic flow velocity, solute retention and column efficiency in open-tubular reversed-phase capillary electrochromatography

被引:33
|
作者
Crego, AL [1 ]
Martínez, J [1 ]
Marina, ML [1 ]
机构
[1] Univ Alcala de Henares, Fac Ciencias, Dept Quim Analit, Madrid 28871, Spain
关键词
electrochromatography; mobile phase composition; electroosmotic flow; efficiency; open-tubular electrochromatography; polynuclear aromatic hydrocarbons;
D O I
10.1016/S0021-9673(99)01243-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The effects of some experimental parameters, such as the volume fraction and type of organic modifier in the mobile phase, and the concentration, type and pH of the buffer on the electroosmotic flow velocity, the retention behavior of test solutes, and the column efficiency have been investigated in capillary electrochromatography (CEC) using an open-tubular column of 9.60 mu m I.D. with a porous silica layer chemically modified with C-18 as stationary phase. The retention of a group of polycyclic aromatic hydrocarbons (PAHs) used as a test mixture varied significantly by changing the organic modifier content in the hydroorganic mobile phase according to the reversed-phase-like selectivity of the stationary phase. In addition, an increase in the percentage of organic modifier resulted in a slight increase in the linear velocity of the EOF. On the other hand, when the phosphate buffer concentration was increased over the range 1-50 mM, the electroosmotic mobility fell dramatically, the retention of the solutes decreased steadily, and the plate height showed a significant increase. The results obtained with phosphate, trishydroxymethylaminomethane or 2-morpholinoethanesulfonic acid as buffers were similar when pH remained constant. Optimization in CEC was essential to achieve further enhancement of separation performance, because the analysis time and separation resolution are essentially affected when varying operating parameters. Separations of seven PAHs with more than 100 000 plates are presented within 4 min analysis time. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:329 / 337
页数:9
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