Insight into the catalytic performance and reaction routes for toluene total oxidation over facilely prepared Mn-Cu bimetallic oxide catalysts

Developing facile preparation method to obtain the satisfied low-temperature catalytic performance of transitional metal oxide-based materials is still a challenge in deep degradation of VOCs. Here, a series of Mn-Cu bimetallic oxide catalysts were prepared by one-step hydrothermal-redox method for catalytic total oxidation of toluene. The CH3COOH concentration, Cu/Mn molar ratio and calcination temperature greatly affected the crystal structure, micromorphology and catalytic performance. Amongst, MnCu spinel structured catalyst exhibited excellent low-temperature catalytic activity, superior durability and water resistance in toluene total oxidation owing to its abundant surface adsorbed oxygen species, higher amount of Cu+ and Mn3+ and excellent low-temperature reducibility. The reaction rate of MnCu was 7.0 times higher than that of MnCu0.5 at 210 ?C. The cyclic redox process with enough oxygen vacancy played a vital role in toluene oxidation. The deep oxidation of benzene was the key step in the toluene oxidation. Proton transfer reaction-mass spectrometry (PTRMS) results revealed the reaction intermediates including benzaldehyde, benzene and phenol, which further decomposed to acetone, ethanol, acetic acid, ketone and acetaldehyde by ring opening before total mineralization. Therefore, PTR-MS provided a facile method to investigate the reaction mechanism of toluene oxidation.

Automated summary

In this study, a series of Mn-Cu bimetallic oxide catalysts were prepared by one-step hydrothermal-redox method for catalytic total oxidation of toluene. The MnCu spinel structured catalyst exhibited excellent low-temperature catalytic activity, superior durability, and water resistance, with a reaction rate 7.0 times higher than that of MnCu0.5 at 210 ?C. The cyclic redox process with enough oxygen vacancy played a vital role in toluene oxidation.