Several solvent extraction systems were studied using a cellulose dialysis membrane as an artificial phase boundary separating one solvent phase from the other. Solutes were allowed to come to extraction equilibrium by permeation through the membrane. The rate of permeation depended on the osmotic properties of the solute, such as the molecular size and the presence of colloidal species. The extraction equilibrium was established by the solvent‐extraction properties of the solute in each system, and the equilibrium was approached through the cellulose membrane by a first‐order kinetic process. The method appears to be useful for ‘packaging’ organic solvents in membrane containers to be used for extractions in which time is not a factor. In certain cases, equally well extracted solutes, such as zirconium and aluminium 8‐hydroxyquinolates, can be separated because one solute exists as a partially colloidal material [Zr(IV)] and hence does not pass through the membrane rapidly.
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Massoumi et al. (1970) studied this question.
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