Toluene oxidation process and proper mechanism over Co3O4 nanotubes: Investigation through in-situ DRIFTS combined with PTR-TOF-MS and quasi in-situ XPS
By Jinping Zhong, Zeng Yikui, Mingyuan Zhang, W. Feng, Diran Xiao, Junliang Wu, Peirong Chen, Mingli Fu, D. Ye. 2020
211 citations recorded by the source corpus.
Abstract Improving catalytic efficiency is a yet still challenge in thermal catalytic oxidation. One of the key issues is to understand its catalytic oxidation mechanism. Here, a series of Co3O4 samples were prepared by solvothermal method. The characterization records showed that nanotubular Co3O4-NTs-2 for its rough surface, low temperature reducibility, abundance of Co3+ ions and surface adsorption oxygen species, thus exhibited high efficiency (T90 = 240℃, Ea = 67.42 kJ/mol) in catalytic oxidation of toluene. In-situ DRIFTS combined PTR-TOF-MS were applied to investigate the reaction process of toluene oxidation. These results revealed that the catalytic oxidation of toluene followed the listed way: toluene → benzyl alcohol → benzaldehyde → benzoate → benzene → phenol → benzoquinone → maleic anhydride and other ring opening by-products like ethanol, acetaldehyde, acetic acid, acetone etc., then ultimately mineralized to CO2 and H2O. Furthermore, the results of quasi in-situ XPS in C7H8/N2, toluene conversion in O2-free evaluation and UV–vis-DRS analysis further confirmed that surface lattice oxygen played an important role in toluene oxidation, and gas-phase oxygen facilitated the reaction. The combination of a series of instruments provided a promising means for further understanding the oxidation mechanism of toluene.
Subfields: Catalysis, Electrical and Electronic Engineering, Materials Chemistry
View Paper: https://www.semanticscholar.org/paper/591a2d7238b0d1e213806548329fa36083434cc1