Open-tubular ion-exchange capillary electrochromatography of inorganic anions

Citation
Mc. Breadmore et al., Open-tubular ion-exchange capillary electrochromatography of inorganic anions, ANALYST, 125(7), 2000, pp. 1235-1241
Citations number
23
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYST
ISSN journal
00032654 → ACNP
Volume
125
Issue
7
Year of publication
2000
Pages
1235 - 1241
Database
ISI
SICI code
0003-2654(2000)125:7<1235:OICEOI>2.0.ZU;2-8
Abstract
The viability of open-tubular ion-exchange electrochromatography (IE-CEC) f or the separation of inorganic anions was investigated. Open-tubular IE-CEC columns were prepared by coating the inner wall of a fused silica capillar y with quaternary ammonium anion-exchange latex particles (approximately 75 nm in diameter) bound electrostatically to the wall. Dionex AS5A latex par ticles were used for this purpose. The coated capillary showed reversed ele ctro-osmotic flow (EOF), allowing anions to be separated in the co-EOF mode . The latex particles on the capillary wall introduced anion-exchange inter actions with the analytes, the strength of which could be moderated by the type and concentration of the competing ion used in the background electrol yte (BGE). With a relatively low concentration of a weak competing ion (e.g ., chloride), the migration order followed that obtained in an anion-exchan ge system. Increasing the concentration of the competing ion resulted in a decrease in the ion-exchange interactions and a change in the migration ord er from that obtained by capillary electrophoresis using a high ionic BGE. A stronger competing ion (e.g., perchlorate or sulfate) suppresses the anio n-exchange interaction at a lower BGE concentration. The effective ion-exch ange capacity of the capillary, and also the resulting anion-exchange inter actions with the analytes, could be increased by decreasing the capillary d iameter. The approaches described in this paper provide a simple means to m anipulate separation selectivity for inorganic anions.