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Surface adsorbed–H2O promoted aerobic oxidation of biomass–derived alcohols on MnOx catalysts.

Authors :
Zhang, Yurong
Wang, Junpeng
Niu, Meiying
Tang, Jun
Chen, Zhipeng
Wan, Chao
Ke, Qingping
Source :
Chemical Engineering Journal. Jun2024, Vol. 490, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

[Display omitted] • Solvent-redox hydrothermal process was employed to constructure MnO x –D oxides. • MnO x –D catalyst exhibites superior catalytic activity for aerobic oxidation of biomass–derived R–CH 2 –OH. • Adsorbed H 2 O on MnO x –D catalyst was found to enhance its superior catalytic activity. Manganese oxides (MnO x) have been emerged as highly active catalysts for the aerobic oxidation of biomass-derived compounds. Herein, a facile urea–redox hydrothermal method was employed to scalable synthesis of MnO x oxides with surface abundant unsaturated Mn and O species. The defective MnO x (MnO x –D) catalyst exhibits remarkable catalytic performance, enabling the room-temperature aerobic oxidation of biomass–derived alcohols with yields exceeding 99%. This represents a substantial 90.8-fold increase in activity compared to commercial MnO 2. Moreover, MnO x –D catalyst demonstrates broad substrate scopes for various biomass–derived alcohols and displays recyclability for the aerobic oxidative conversion of 5-hydroxymethylfurfural (HMF) over five cycles. Through a comprehensive analysis involving X–ray photoelectron spectroscopy (XPS), in–situ infrared (IR) spectroscopy, and controlled experiments, it is established that the presence of surface–adsorbed H 2 O species on MnO x –D catalyst significantly influences its catalytic performance. Mechanism studies reveal that the aerobic oxidation of biomass–derived R–CH 2 –OH compounds into the corresponding aldehydes can proceed via radical and non–radical pathways. Notably, the catalytic activity of MnO x –D catalyst in both pathways is mediated by the surface adsorbed H 2 O species. In the radical route, surface adsorbed H 2 O and O 2 species are converted into active •OH radical species, while in the non–radical route, surface adsorbed H 2 O can form a complex of HMF––H 2 O species. Both processes enhance the abstraction of H from the O–H and C–H bonds in the R–CH 2 –OH compounds on MnO x –D catalyst. This discovery could potentially guide the development of efficient metal oxidic catalysts for the oxidation of biomass–derived R–CH 2 –OH compounds. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13858947
Volume :
490
Database :
Academic Search Index
Journal :
Chemical Engineering Journal
Publication Type :
Academic Journal
Accession number :
177419842
Full Text :
https://doi.org/10.1016/j.cej.2024.151721