Monitoring the electroosmotic flow in capillary electrophoresis using contactless conductivity detection and thermal marks

被引:23
作者
Saito, Renata Mayumi [1 ]
Neves, Carlos Antonio [1 ]
Lopes, Fernando Silva [1 ]
Blanes, Lucas [1 ]
Alves Brito-Neto, Jose Geraldo [1 ]
do Lago, Claudimir Lucio [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, BR-05508000 Sao Paulo, Brazil
关键词
D O I
10.1021/ac0615293
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The fundamental aspects and the capillary electrophoresis usage of thermal marks are presented. The so-called thermal mark is a perturbation of the electrolyte concentration generated by a punctual heating of the capillary while the separation electric field is maintained. The heating pulse is obtained by powering tungsten filaments or surface mount device resistors with 5 V during a few tens to hundreds of milliseconds. In the proposed model, the variation of the transport numbers with the rising temperature leads to the formation of low- and high-concentration regions during the heating. After cooling down, the initial mobilities of the species are restored and these regions (the thermal mark) migrate chiefly due to the electroosmotic flow (EOF). The mark may be recorded with a conductivity detector as part of a usual electropherogram and be used to index the analyte peaks and thus compensate for variations of the EOF. In a favorable case, 10 mmol/L KCl solution, the theory suggests that the error in the measurement of EOF mobility by this mean is only -6.5 x 10(-7) cm(2) V-1 s(-1). The method was applied to the analysis of alkaline ions in egg white, and the relative standard deviations of the corrected mobilities of these ions were smaller than 1%. This is a challenging matrix, because albumin reduces the EOF to 20% of its initial value after 11 runs. The combination of thermal mark, electrolysis separated, and contactless conductivity detection allowed the measurement of the EOF of a silica capillary with unbuffered KCl solution with constant ionic strength. The overall approach is advantageous, because one can easily control the chemical composition of the solution in contact with the inner surface of the capillary.
引用
收藏
页码:215 / 223
页数:9
相关论文
共 26 条
[1]  
CONWAY BE, 1952, ELECTROCHEMICAL DATA, P139
[2]  
da Silva JAF, 2002, J CHROMATOGR A, V942, P249
[3]  
da Silva JAF, 1998, ANAL CHEM, V70, P4339
[4]   Extending the lifetime of the running electrolyte in capillary electrophoresis by using additional compartments for external electrolysis [J].
de Jesus, DP ;
Brito-Neto, JGA ;
Richter, EM ;
Angnes, L ;
Gutz, IGR ;
do Lago, CL .
ANALYTICAL CHEMISTRY, 2005, 77 (02) :607-614
[5]   Method for measuring very weak, residual electroosmotic flow in coated capillaries [J].
Ermakov, SV ;
Capelli, L ;
Righetti, PG .
JOURNAL OF CHROMATOGRAPHY A, 1996, 744 (1-2) :55-61
[6]   System zones in capillary zone electrophoresis [J].
Gas, B ;
Kenndler, E .
ELECTROPHORESIS, 2004, 25 (23-24) :3901-3912
[7]   MECHANISTIC STUDIES OF ELECTROOSMOTIC CONTROL AT THE CAPILLARY SOLUTION INTERFACE [J].
HUANG, TL ;
TSAI, P ;
WU, CT ;
LEE, CS .
ANALYTICAL CHEMISTRY, 1993, 65 (20) :2887-2893
[8]   Eigenmobilities in background electrolytes for capillary zone electrophoresis:: IV.: Computer program PeakMaster [J].
Jaros, M ;
Hruska, V ;
Stedry, M ;
Zusková, I ;
Gas, B .
ELECTROPHORESIS, 2004, 25 (18-19) :3080-3085
[9]   Apparent baseline irregularities for neutral markers in capillary zone electrophoresis with electroosmotic flow [J].
KenndlerBlachkolm, K ;
Popelka, S ;
Gas, B ;
Kenndler, E .
JOURNAL OF CHROMATOGRAPHY A, 1996, 734 (02) :351-356
[10]   Zeta potential of microfluidic substrates: 2. Data for polymers [J].
Kirby, BJ ;
Hasselbrink, EF .
ELECTROPHORESIS, 2004, 25 (02) :203-213