Density functional theories of solvation forces in charged fluids are extended to treat electrolytes consisting of finitesized ions and neutral solvent particles. The resulting forces display pronounced oscillations whose magnitude is a strong function of the bulk density of the neutral species.
Forces between Carboxylic Acid Surfaces in Divalent Electrolyte Solutions
โ Scribed by Thomas Ederth; Per M. Claesson
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 84 KB
- Volume
- 229
- Category
- Article
- ISSN
- 0021-9797
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โฆ Synopsis
The behavior of self-assembled monolayers of thiohexadecanoic acid adsorbed onto gold interacting in asymmetric 2:1 electrolytes has been studied with direct force measurements. The effects of two divalent cations (Mg(2+) and Ca(2+)) were studied at concentrations ranging from 1 ยตM to 10 mM. As compared to interactions in the presence of Na(+), the divalent ions adsorb strongly to the surfaces, with the effect of lowering the surface potential and decreasing the double-layer repulsion. At concentrations above 10 ยตM, the Ca(2+) ions were found to adsorb stronger than Mg(2+). Ca(2+) ions cause charge reversal at high concentrations, and the net interactions at 10 mM were attractive over the measurable range. Copyright 2000 Academic Press.
๐ SIMILAR VOLUMES
The forces between two molecularly smooth mica surfaces were measured over a range of concentrations in aqueous Li -+, Na+, Kf and Cs\* chloride solutions. Deviations from DLVO forces in the form of additional short-range repulsive "hydration" forces were observed only above some critical bulk conce
We have investigated the forces between two surfaces, immersed in a dilute electrolyte solution, interacting specifically with the ions that are in their immediate vicinity. It is found that at large separations the free energy decays exponentially (the decay length being approximately half the Deby