Use of coupled open-tubular capillaries for in-line ion-exchange preconcentration of anions by capillary electrochromatography with elution by a transient isotachophoretic gradient

被引:26
作者
Hutchinson, JP
Macka, M
Avdalovic, N
Haddad, PR
机构
[1] Univ Tasmania, ACROSS, Sch Chem, Hobart, Tas 7001, Australia
[2] Dionex Chem Corp, Sunnyvale, CA 94088 USA
关键词
electrochromatography; capillary columns; isotachophoretic gradients; water analysis; environmental analysis; coupled columns; inorganic anions;
D O I
10.1016/j.chroma.2004.03.073
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Open-tubular capillaries have been joined together for use in on-column ion-exchange preconcentration of anions by capillary electrochromatography (CEC) with elution by a transient isotachophoretic gradient. This involved the coupling of a preconcentration capillary and a separation capillary using a PTFE sleeve. Such coupling allowed precise lengths of differently coated capillaries to be joined in-line to form a single multi-mode column. The different segments could be tailored to optimize a separation by either altering the length of each segment to precisely manipulate the amount of stationary phase present or by changing the internal diameter of each segment to alter the phase ratio in the chromatographic column without affecting the path length for UV detection. In this work, a segmented in-line capillary was used in conjunction with a fluoride-octanesulfonate discontinuous electrolyte system to increase the number of anions that could be preconcentrated and separated. Quaternary ammonium functionalised latex particles were used for creating the preconcentration segment and the separation segment was coated with poly(diallyldimethylammonium chloride). This allowed the detection of trace anions in drinking water and in situ sampling of river water for the analysis of trace inorganic anions. The repeatability of producing the quaternary ammonium functionalized latex-coated segments was assessed and the effect of segmentation on peak efficiency was investigated. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:187 / 192
页数:6
相关论文
共 48 条
[11]   SELECTIVE ONLINE PRECONCENTRATION OF PROTEINS BY TANDEM METAL CHELATE-CAPILLARIES CAPILLARY-ZONE ELECTROPHORESIS [J].
CAI, JY ;
ELRASSI, Z .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1993, 16 (9-10) :2007-2024
[12]  
Chien R. L., 1992, ANAL CHEM, V64, P489
[13]   SAMPLE STACKING OF AN EXTREMELY LARGE INJECTION VOLUME IN HIGH-PERFORMANCE CAPILLARY ELECTROPHORESIS [J].
CHIEN, RL ;
BURGI, DS .
ANALYTICAL CHEMISTRY, 1992, 64 (09) :1046-1050
[14]   ON-COLUMN TRANSIENT AND COUPLED COLUMN ISOTACHOPHORETIC PRECONCENTRATION OF PROTEIN SAMPLES IN CAPILLARY ZONE ELECTROPHORESIS [J].
FORET, F ;
SZOKO, E ;
KARGER, BL .
JOURNAL OF CHROMATOGRAPHY, 1992, 608 (1-2) :3-12
[15]  
Foret F, 1990, J MICROCOLUMN SEP, V2, P229
[16]   THE USE OF A CONCENTRATION STEP TO COLLECT URINARY COMPONENTS SEPARATED BY CAPILLARY ELECTROPHORESIS AND FURTHER CHARACTERIZATION OF COLLECTED ANALYTES BY MASS-SPECTROMETRY [J].
GUZMAN, NA ;
TREBILCOCK, MA ;
ADVIS, JP .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1991, 14 (05) :997-1015
[18]   NEW APPROACHES TO CONCENTRATION ON A MICROLITER SCALE OF DILUTE SAMPLES, PARTICULARLY BIOPOLYMERS WITH SPECIAL REFERENCE TO ANALYSIS OF PEPTIDES AND PROTEINS BY CAPILLARY ELECTROPHORESIS .1. THEORY [J].
HJERTEN, S ;
LIAO, JL ;
ZHANG, R .
JOURNAL OF CHROMATOGRAPHY A, 1994, 676 (02) :409-420
[19]   BIAS IN QUANTITATIVE CAPILLARY ZONE ELECTROPHORESIS CAUSED BY ELECTROKINETIC SAMPLE INJECTION [J].
HUANG, XH ;
GORDON, MJ ;
ZARE, RN .
ANALYTICAL CHEMISTRY, 1988, 60 (04) :375-377
[20]   Enantiomeric separation by capillary electrophoresis with an electroosmotic flow-controlled capillary [J].
Katayama, H ;
Ishihama, Y ;
Asakawa, N .
JOURNAL OF CHROMATOGRAPHY A, 2000, 875 (1-2) :315-322