Micellar effect on the reaction of picolinic acid catalyzed chromium(VI) oxidation of dimethyl sulfoxide in aqueous acidic media: A kinetic study

Abstract

The kinetics and mechanism of picolinic acid (PA) catalyzed oxidation of dimethyl sulfoxide (DMSO) to dimethyl sulfone by chromium(VI) in both aqueous H2SO4 and HClO4 media have been studied in the absence and presence of surfactants at different temperatures. Cr(VI)–PA complex formed in preequilibrium steps is the active oxidant that experiences the nucleophilic attack by DMSO to form a positively charged intermediate ternary complex. Within the proposed ternary complex, an oxygen transfer or a ligand coupling or both occurs to generate the product, dimethyl sulfone. Cr(VI) is ultimately converted to Cr(III)–PA complex. Under the experimental conditions, the process shows a first-order dependence on each of the reactants (i.e., [Cr(VI)]T, [PA]T, [DMSO]T, and [H+]). HCrO4− has been found kinetically active. The reaction is catalyzed by sodium dodecyl sulfate (SDS, a representative anionic surfactant) monotonically, while cetylpyridinium chloride (CPC, a representative cationic surfactant) retards the reaction continuously. The observed micellar effects have been explained by considering the hydrophobic and electrostatic interaction between the surfactants and reactants. A pseudo-phase ion exchange (PIE) model has been applied to explain the micellar effect. The Piszkiewicz cooperative model has been applied to determine the kinetic parameters, and it indicates the existence of catalytically productive submicellar aggregates. Because of this reactant-promoted micellization of the surfactant before or below the cmc value, the present systems do not show any discontinuity at the respective reported cmc values of the surfactants. © 2001 John Wiley & Sons, Inc. Int J Chem Kinet 33: 173–181, 2001