A natural sodium bentonite was tested in the laboratory to measure its reflection coefficient, ω, in equilibrium with mixed aqueous solutions of sodium chloride (NaCl) and potassium chloride (KCl), with the aim of assessing the relative contribution of chemico-osmosis and diffusion induced electro-osmosis to the non-hydraulic component of the liquid flux in the presence of two cationic species, which diffuse at different rates in the pore solution. The former chemico-osmotic contribution is only related to the ionic partition effect in the bentonite pores, and causes ω to vary in the 0 to 1 range, whereas the latter electro-osmotic contribution is controlled by the diffusion potential, which spontaneously builds up across the bentonite layer in response to the different aqueous-phase diffusion coefficients of the ionic species. The theoretical interpretation of the obtained test results demonstrated that chemico-osmosis was the major contribution to ω when the testing solutions only comprised KCl. However, significant deviations in the values of ω from those expected for pure chemico-osmosis were observed for mixtures of NaCl and KCl, with both negative (ω = −1.234) and positive (ω = 1.040) anomalous values of the reflection coefficient, resulting from the enhanced influence of diffusion induced electro-osmosis.
Reflection coefficient of a natural sodium bentonite in aqueous mixed electrolyte solutions: positive and negative anomalous osmosis / Guarena, Nicolo; Dominijanni, Andrea; Manassero, Mario. - In: CANADIAN GEOTECHNICAL JOURNAL. - ISSN 0008-3674. - STAMPA. - (In corso di stampa). [10.1139/cgj-2024-0119]
Reflection coefficient of a natural sodium bentonite in aqueous mixed electrolyte solutions: positive and negative anomalous osmosis
Guarena, Nicolo;Dominijanni, Andrea;Manassero, Mario
In corso di stampa
Abstract
A natural sodium bentonite was tested in the laboratory to measure its reflection coefficient, ω, in equilibrium with mixed aqueous solutions of sodium chloride (NaCl) and potassium chloride (KCl), with the aim of assessing the relative contribution of chemico-osmosis and diffusion induced electro-osmosis to the non-hydraulic component of the liquid flux in the presence of two cationic species, which diffuse at different rates in the pore solution. The former chemico-osmotic contribution is only related to the ionic partition effect in the bentonite pores, and causes ω to vary in the 0 to 1 range, whereas the latter electro-osmotic contribution is controlled by the diffusion potential, which spontaneously builds up across the bentonite layer in response to the different aqueous-phase diffusion coefficients of the ionic species. The theoretical interpretation of the obtained test results demonstrated that chemico-osmosis was the major contribution to ω when the testing solutions only comprised KCl. However, significant deviations in the values of ω from those expected for pure chemico-osmosis were observed for mixtures of NaCl and KCl, with both negative (ω = −1.234) and positive (ω = 1.040) anomalous values of the reflection coefficient, resulting from the enhanced influence of diffusion induced electro-osmosis.Pubblicazioni consigliate
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https://hdl.handle.net/11583/2995767
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