Abstract
Catalytic deoxygenation represents a straightforward and core methodology for fine-chemical production and biomass upgrading. Generally, the application of homogeneous metal complexes or heterogeneous noble-metal catalysts prevails in academia and the chemical industry. Herein, we introduce cobalt@ordered mesoporous carbon (Co@OMC) catalysts, which are constructed conveniently by a mechanochemical coordination self-assembly based on a renewable tannin precursor. Importantly, the Co@OMC catalysts with a high loading of in situ confined Co species promote the selective deoxygenation of various ketones, aldehydes, and alcohols efficiently into the corresponding alkanes under mild conditions. Therefore, a simple, inexpensive, and heterogeneous catalyst for selective deoxygenation can be expected, meanwhile the solid-state synthesis affords a green, rapid, and scalable pathway to Co@OMC catalysts.
Original language | English |
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Pages (from-to) | 3299-3304 |
Number of pages | 6 |
Journal | ChemCatChem |
Volume | 10 |
Issue number | 15 |
DOIs | |
State | Published - Aug 13 2018 |
Funding
S.D., N.C., and P.F.Z. were supported by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, U. S. Department of Energy. Electron microscopy at ORNL (S.Z.Y.) was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division and performed in part as a user project proposal at the ORNL Center for Nanophase Materials Sciences, which is a DOE Office of the Science User Facility Facilities. P.F.Z. acknowledges the Shanghai Pujiang Program (Grant No. 17PJ1403500), National Natural Science Foundation of China (Grant No. 21776174) and the Thousand Talent Program of China for support.
Keywords
- cobalt
- heterogeneous catalysis
- hydrogenation
- mesoporous materials
- nanoparticles