The adsorption of surfactant-alcohol mixtures at the silica-water interface
was studied by means of ellipsometry. The results show that addition of ev
en small amounts of alcohol can have large effects on the characteristics o
f the adsorbed layer. For example, a 20% replacement of the octa(ethylene g
lycol) dodecyl (C12E8) surfactants by dodecanol results in an increase in t
he total surface excess of 80%. The thickness of the adsorbed layer, on the
other hand, is virtually unaffected by the alcohol being added. Hence, as
the alcohol content increases, the adsorbed surfactant aggregates at the si
lica-water interface mainly grow in the surface plane. A surfactant such as
C12E5, which forms relatively large surface aggregates from the start, can
only solubilize a small fraction of the long-chain alcohols before the sys
tem phase separates. This fraction was found not to result in any major str
uctural changes in the surface layer. These findings are discussed in terms
of surfactant packing and in relation to observations in bulk solutions re
ported earlier. Our study also includes measurements of adsorption and deso
rption kinetics for both the surfactant and the surfactant-alcohol systems.
The main finding is that the effect of alcohol is most obvious in the deso
rption kinetics. We conclude that the effects observed are due to differenc
es between the surfactant and the alcohol in monomer solubility.