Reaction pathway of the catalytic wet air oxidation of phenol with a Fe/activated carbon catalyst

Abstract

Catalytic wet air oxidation (CWAO) of phenol with molecular oxygen using a home-made Fe/activated carbon catalyst at mild operating conditions (100–127°C; 8atm) has been studied in a trickle-bed reactor. Ring compounds (hydroquinone, p-benzoquinone and p-hydroxybenzoic acid) and short-chain organic acids (maleic, malonic, oxalic, acetic and formic) have been identified as intermediate oxidation products. CWAO experiments using each one of these intermediates as starting compound have been carried out (at 127°C and 8atm) in order to elucidate the reaction pathway. It was found that phenol is oxidized through two different ways. It can be either para-hydroxylated to hydroquinone, which is instantaneously oxidized to p-benzoquinone or para-carboxylated to p-hydroxybenzoic acid. p-Benzoquinone is majorly mineralized to CO2 and H2O through oxalic acid formation whereas p-hydroxybenzoic acid gives rise to short-chain acids. Only acetic acid showed to be refractory to CWAO under the operating conditions used in this work. The catalyst avoids the presence of ring-condensation products in the reactor effluent which were formed in absence of it. This is an additional important feature because of the ecotoxicity of such compounds.