1980•Soil Science Society of America JournalRequires access

Sodium/Calcium Exchange in Montmorillonite and Illite Suspensions

I. Shainberg, James D. Oster, J. D. Wood

Open publisher page 89 citations

Abstract

Abstract The effect of salt concentration and exchanger composition on Na/Ca exchange in montmorillonite and illite suspensions (0.02 to 0.08 g clay/g water) was studied, where the equivalent fraction of exchangeable Ca, E Ca , ranged from 0.6 to 1. A theoretical evaluation based on double‐layer theory for montmorillonite indicates that the formation of tactoids and internal surfaces at the Ca 3+ end of the exchange isotherm can cause the Vanselow selectivity coefficient, K V , to depend on exchangeable cation composition and total electrolyte concentration. Whereas for montmorillonite, K V increased with E Ca (0.6 < E Ca < 1), as predicted for internal surfaces, the reverse was true for illite, where external surfaces predominate. Likewise, for a given Na adsorption ratio, dilution of the equilibrium solution for illite (0.6 < E Ca < 1) and for montmorillonite ( E Ca ≃ 0.6) decreased K V as predicted for external surfaces. The average Gapon selectivity coefficient for the montmorillonite (0.011) and illite clays (0.023) with E Ca ≤ 0.8, suggests that the value for soils, (0.0148) reflects their mixed mineralogy.

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What this paper is about

Abstract The effect of salt concentration and exchanger composition on Na/Ca exchange in montmorillonite and illite suspensions (0.02 to 0.08 g clay/g water) was studied, where the equivalent fraction of exchangeable Ca, E Ca , ranged from 0.6 to 1. A theoretical evaluation based on double‐layer theory for montmorillonite indicates that the formation of tactoids and internal surfaces at the Ca 3+ end of the exchange isotherm can cause the Vanselow selectivity coefficient, K V , to depend on exchangeable cation composition and total electrolyte concentration. Whereas for montmorillonite, K V increased with E Ca (0.6 < E Ca < 1), as predicted for internal surfaces, the reverse was true for illite, where external surfaces predominate. Likewise, for a given Na adsorption ratio, dilution of the equilibrium solution for illite (0.6 < E Ca < 1) and for montmorillonite ( E Ca ≃ 0.6) decreased K V as predicted for external surfaces. The average Gapon selectivity coefficient for the montmorillonite (0.011) and illite clays (0.023) with E Ca ≤ 0.8, suggests that the value for soils, (0.0148) reflects their mixed mineralogy.

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Available abstract

Abstract The effect of salt concentration and exchanger composition on Na/Ca exchange in montmorillonite and illite suspensions (0.02 to 0.08 g clay/g water) was studied, where the equivalent fraction of exchangeable Ca, E Ca , ranged from 0.6 to 1. A theoretical evaluation based on double‐layer theory for montmorillonite indicates that the formation of tactoids and internal surfaces at the Ca 3+ end of the exchange isotherm can cause the Vanselow selectivity coefficient, K V , to depend on exchangeable cation composition and total electrolyte concentration. Whereas for montmorillonite, K V increased with E Ca (0.6 < E Ca < 1), as predicted for internal surfaces, the reverse was true for illite, where external surfaces predominate. Likewise, for a given Na adsorption ratio, dilution of the equilibrium solution for illite (0.6 < E Ca < 1) and for montmorillonite ( E Ca ≃ 0.6) decreased K V as predicted for external surfaces. The average Gapon selectivity coefficient for the montmorillonite (0.011) and illite clays (0.023) with E Ca ≤ 0.8, suggests that the value for soils, (0.0148) reflects their mixed mineralogy.

Key concepts: Montmorillonite, Illite, Dilution, Chemistry, Ion exchange, Adsorption, Sodium, Clay minerals

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