SALTING-IN BY QUATERNARY AMMONIUM SALTS

Abstract
The solubility of benzene in substituted quaternary ammonium bromide solutions has been measured by ultraviolet absorption. The solubility is found to increase in the presence of such salts as R4−nHnN+Br where R is an alkyl group and n varies between 0 and 3; a smooth transition in behavior is observed when passing from simple salts to long-chained micellar salts. This salting-in can be explained in terms of an association between the nonelectrolyte and the quaternary ammonium ion, which is induced by the increase in the structure of water near large nonpolar groups of the organic ions.