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Methanol Oxidative Dehydrogenation and Dehydration on Carbon Nanotubes: Active Sites and Basic Reaction Kinetics

Abstract

Methanol dehydrogenation to formaldehyde or dehydration to dimethyl ether are high-value-added industrial processes. Here we applied oxidized multi-walled carbon nanotubes (oCNT) in methanol conversion reaction in the presence of oxygen. oCNT catalysts exhibit methanol conversion of 60 % under gentle reaction conditions, yielding DME (65%) and FA (30%) as the main products, and long term stability for over 150 h is achieved. The catalytic performance of oCNT is even comparable to industrial metal catalysts. The in-situ site titration experiment revealed that carboxyl groups were the active sites for the formation of dimethyl ether. Small organic molecules as model catalysts suggested that quinoidic carbonyl groups may be responsible for methanol ODH producing formaldehyde, while both quinoidic and ketonic carbonyl groups are responsible for total oxidation to carbon dioxide. The basic reaction kinetics and mechanism such as reaction orders, apparent activation energy and rate determining step etc. for the oxidative dehydrogenation and dehydration of methanol were studied systematically. A unique gentle redox catalytic activity of oCNT catalysts could be realized to reduce the over-oxidation losses.

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Supplementary files

Article information


Submitted
27 Mar 2020
Accepted
11 May 2020
First published
12 May 2020

Catal. Sci. Technol., 2020, Accepted Manuscript
Article type
Paper

Methanol Oxidative Dehydrogenation and Dehydration on Carbon Nanotubes: Active Sites and Basic Reaction Kinetics

P. Yan, X. Zhang, F. Herold, F. Li, X. Dai, T. Cao, B. J. M. Etzold and W. Qi, Catal. Sci. Technol., 2020, Accepted Manuscript , DOI: 10.1039/D0CY00619J

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