Abstract
Cd(HSal)2 is extracted from aqueous solutions into n-butanol, but not into non-hydroxylic solvents (such as benzene and chloroform) at pH 4.5 to 6.0. Addition of N bases, which have no effect alone, causes extraction into the latter solvents, apparently by displacement of coordinated water, giving Cd(HSal)2•2B. This synergistic effect varies with B (β-picoline > pyridine > quinoline). Formation and distribution constants are given for the experimental conditions.
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