Liquid phase selective oxidation of benzene over nanostructured Cu(x)Ce(1-x)O(2-delta) (0.03 less than or equal to x less than or equal to 0.15)

Abstract

Liquid phase direct oxidation of benzene to phenol was carried out over copper loaded on oxides such as ceria, alumina, magnesia, ferric oxide, zinc oxide with 30 percent H(2)O(2) as oxidant under atmospheric pressure. Of all the catalytic formulations prepared via a novel solution combustion synthesis, the ceria based catalysts showed highest activity. Particularly, over the Cu(0.10)Ce(0.90)O(2-delta) catalyst, 43 percent conversion of benzene with 100 percent selectivity was observed at 70 degrees C and atmospheric pressure. The activity of this combustion synthesized catalyst is also higher than the corresponding catalyst prepared by incipient wetness impregnation and coprecipitation methods. Powder XRD, TEM and XPS studies show ionically substituted copper over ceria as the predominant phase in the combustion derived catalyst whereas on the impregnated and coprecipitated catalysts copper is present in the dispersed copper oxide form. Influences of temperature and time, H(2)O(2) concentration and solvent have also been investigated. Enhanced activity over the combustion synthesized catalyst wherein Cu2+ ion is present as substitutional ion in ceria has been attributed to Cu-O-Ce ionic interaction. Ionic substitution also brings stability to the active copper ion component in the combustion synthesized catalyst with lower risk of Cu-leaching as compared to the corresponding impregnated and coprecipitated catalysts as evidenced from the recycling experiments.