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Physicochemical criteria for reverse osmosis separation of alcohols, phenols, and monocarboxylic acid in aqueous solutions using porous cellulose acetate membranes
Author(s) -
Matsuura Takeshi,
Sourirajan S.
Publication year - 1971
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1971.070151202
Subject(s) - chemistry , membrane , aqueous solution , dissociation (chemistry) , phenols , reverse osmosis , cellulose acetate , molecule , organic chemistry , substituent , cellulose , acid dissociation constant , chromatography , inorganic chemistry , biochemistry
Reverse osmosis data of 32 different alcohols and phenols and 22 different monocarboxylic acids in aqueous solutions in the concentration range 0.0001 to 0.007 M (∼100 ppm in most cases) have been studied using porous cellulose acetate membranes at 250 psig. Solute separation data for alcohols and phenols are correlated with Δν s (shift in the OH band maximum in the IR spectra), and those for the monocarboxylic acids are correlated with K a (dissociation constant) and the degree of dissociation of the molecule. Solute separation decreases with increase in Δν s for alcohols and phenols. The solute separation‐versus‐ K a correlation for acids passes through a minimum, and solute separation always increases with increase in the degree of dissociation. The separation data are also correlated with Taft and Hammett numbers which represent the effect of the substituent group on the polar effect of the molecule. The product rate data show a general tendency to decrease with decrease in solute separation in all cases. These results show that, with respect to the systems considered, solute separation in reverse osmosis is governed by the hydrogen bonding ability of the organic molecule when it is essentially undissociated and by electrostatic repulsion of ions when the molecule is partially or completely dissociated. Thus, data on Δν s for alcohols and phenols, and those on K a and degree of dissociation for monocarboxylic acids, constitute precise physicochemical criteria for reverse osmosis separation of the above solutes in aqueous solutions using porous cellulose acetate membranes.