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.