The binding of an anionic surfactant
onto an anionic surface by
addition of divalent ions is reported based on experimental data from
specular neutron reflection (NR) and attenuated total internal reflection
IR spectroscopy (ATR-IR). Similar measurements using monovalent ions
(sodium) do not show any evidence of such adsorption, even though
the amount of surfactant can be much higher. This data is interpreted
in terms of the so-called bridging mechanism of ion binding.
Neutron reflectometry has been used to study the adsorption of the anionic surfactant bis(2-ethylhexyl) sulfosuccinate cesium salt on the anionic surface of mica. Evidence of significant adsorption is reported. The adsorption is reversible and changes little with pH. This unexpected adsorption behavior of an anionic molecule on an anionic surface is discussed in terms of recent models for surfactant adsorption such as cation bridging, where adsorption has been reported with the divalent ion calcium but not previously observed with monovalent ions.
The adsorption of a phosphorus analogue of the surfactant AOT, sodium bis(2-ethylhexyl) phosphate (NaDEHP), at the water/alumina interface is described. The material is found to adsorb as an essentially water-free bilayer from neutron reflection measurements. This is similar to the behavior of AOT under comparable conditions, although AOT forms a thicker, more hydrated layer. The NaDEHP shows rather little variation with added salt, but a small thickening of the layer on increasing the pH, in contrast to the behavior of AOT.
We report an investigation of the presence of thin water layers on calcium carbonate particles dispersed in cyclohexane using small-angle neutron scattering. We identify an adsorbed water layer and measure the thickness using contrast variation to optimize the sensitivity of the scattering to the water. We also report the variation in thickness of these water layers in the presence of salt solutions with the variation of salt concentration and valency. We conclude that thin water layers can be observed using SANS; however, the layers are thin and correspond to essentially the hydration of the particle surfaces.
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