A theoretical model for electroosmotic mobility (mu(eo)) in argentation cap
illary electrophoresis has been established and the effects of buffer pH, A
g(I) concentration, temperature and organic solvent on electroosmotic mobil
ity investigated. The decrease in mu(eo) with increasing Ag(I) concentratio
n is the sum of the decrease in the double layer thickness and the reductio
n in the surface charge density due to the electrostatic interaction or che
lation between Ag(I) and the charged surface groups. A characteristic disso
ciation constant of 0.032 mM was obtained for the Ag(I)-siloxide complex fr
om the experimental results. This constant is much smaller than the corresp
onding value for the sodium ion.