A model is presented that describes the effect of pH on the
adsorption of an isomerically pure
anionic surfactant species at a mineral oxide/water interface. A
site-binding model, to account
for effects of pH, surface heterogeneities, and counterions, is
incorporated into a patchwise, phase-separation modeling approach, making it possible to predict both the
surface charge and the
counterion association beneath an adsorbed surfactant aggregate.
Parameters for the site binding
model on α-alumina are obtained from experimental surface charge
measurements. The
formation of both local monolayers (hemimicelles) and bilayers
(admicelles) is allowed, although
the isotherms studied in this paper are fit by parameter values that
predict admicelle formation
only. The model is able to predict experimental measurements of
the adsorption of an
isomerically pure, anionic surfactant species on α-alumina as a
function of pH. It reproduces
several previously unexplained experimental observations; in
particular, it offers an explanation
for the observation of significant adsorption of anionic surfactant
above the point of zero charge
(pzc) of a mineral oxide surface.