Abstract

The enhancement in the autoxidation of ethylbenzene by molecular oxygen in the presence of quaternary ammonium salts (QAS) was investigated from the experimental and theoretical points of view. The primary effect of the addition of QAS to the reaction medium was an increase in ethylbenzene conversion. Quantum chemical calculations, using B3LYP hybrid functional, revealed a weakening of C–O and O–H bonds of the hydroperoxide. These effects favor the formation of ethylbenzenyl and peroxyl radicals, respectively, both of which are involved in the propagation reaction that leads to the formation of hydroperoxide, the desired final product.

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