1977
DOI: 10.1071/sr9770121
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Ionic adsorption on variable charge mineral surfaces. Theoretical charge development and titration curves

Abstract: A completely general theory is presented which can be used to describe both anion and cation adsorption on amphoteric oxide surfaces. It takes account of the fact that both the surfaces and adsorbing species are charged and that the surfaces change their charge when ionic adsorption takes place. The theory is applicable to both specific and non-specifically adsorbed ions. It is shown to account for the pH dependent charge curves of goethite, silica and two tropical soils.

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Cited by 98 publications
(159 citation statements)
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“…The term ai can be replaced by α γ c, where α is the proportion of the ion, γ is the coefficient of activity and c is the ion concentration in solution. The activity ais is equal to the quantity of occupied sites in relation to available sites, that is θ/ (1-θ), in which θ is the proportion of occupied sites (Bowden et al, 1977). Then: By using FLM, we can obtain adjustable parameters, the ion bonding constant to colloidal surfaces K, and the soil surface electric potential.…”
Section: Four-layer Model (Flm)mentioning
confidence: 99%
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“…The term ai can be replaced by α γ c, where α is the proportion of the ion, γ is the coefficient of activity and c is the ion concentration in solution. The activity ais is equal to the quantity of occupied sites in relation to available sites, that is θ/ (1-θ), in which θ is the proportion of occupied sites (Bowden et al, 1977). Then: By using FLM, we can obtain adjustable parameters, the ion bonding constant to colloidal surfaces K, and the soil surface electric potential.…”
Section: Four-layer Model (Flm)mentioning
confidence: 99%
“…The neutral surface of FLM is represented by OH-S-OH 2 in which the surface electric potential decreases due to an increase of soil acidity (equation 71), but increases when pH becomes higher (equation 72) (Bowden et al, 1977).…”
Section: Four-layer Model (Flm)mentioning
confidence: 99%
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“…The magnitude of the constant charge is independent on pH and the ionic strength of the solution, given that under these conditions there is no decomposition of the crystal lattice of minerals, which likely happens in the case of synthesis of the preparations (Thomas & Hargrove, 1984). The changeable constant-potential charge is also characteristic of aluminum oxides and hydroxides, silica oxides and amphoteric aluminum, and iron oxides and hydroxyoxides (Bowden et al, 1977).…”
Section: Introductionmentioning
confidence: 99%
“…They were applied to the reaction of synthetic oxides with anions (Bowden et al 1977;Barrow et al 1980a, b;Sposito 1983;Bolan and Barrow 1984;Barrow 1987;Barrow and Bowden 1987;Schindler and Stumm 1987). The surface complexation models differ from each other in two distinct aspects: 1) in the number of planes that are specified and hence in the allocation of ions to the planes, and 2) in the way the surface reaction is modeled.…”
mentioning
confidence: 99%