Benzene Oxidation with Ozone Over MnO(x)/MSU-H and MnO(x)/Mesoporous-SAPO-34 Catalysts
Abstract:
Two mesoporous silica materials, MSU-H and mesoporous SAPO-34 (Meso-SAPO-34), were applied to the catalytic oxidation with ozone of benzene. The catalysts were characterized by X-ray diffraction, N2 adsorption-desorption, Brunauer-Emmett-Teller specific surface area, and H2-temperature programmed reduction. When MnO(x)/MSU-H was used at three different temperature, 50 degrees C, 80 degrees C, and 100 degrees C, the ozone conversion and CO(x) yield increased with increasing temperature. MnO(x)/MSU-H exhibited much higher catalytic activity than that of MnO(x)/Meso-SAPO-34. The high catalytic activity of MnO(x)/MSU-H seems to be due to the high oxygen ability and structural stability of MSU-H. The CO2 yield was somewhat enhanced by the addition of steam because steam facilitated desorption of the reaction intermediates adsorbed on the catalyst surface, enabling them to be oxidized further.
Related Concept Videos
Reactions at the Benzylic Position: Oxidation and Reduction
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Radical Oxidation of Allylic and Benzylic Alcohols
Electrophilic Aromatic Substitution: Nitration of Benzene
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation


