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A promising low pressure methanol synthesis route from CO2 hydrogenation over Pd@Zn core–shell catalysts
Authors:
Edman
Tsang
(Wolfson Catalysis Centre, Department of Chemistry, University of Oxford)
,
Fenglin
Liao
(Wolfson Catalysis Centre, Department of Chemistry, University of Oxford)
,
Xin-Ping
Wu
(Key Laboratory for Advanced Materials, Centre for Computational Chemistry and Research Institute of Industrial Catalysis, College of Chemistry and Molecular Engineering, East China University of Science and Technology)
,
Jianwei
Zheng
(State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Production of Alcohols-Ethers-Esters, iChEM, College of Chemistry and Chemical Engineering, Xiamen University)
,
Molly Meng-Jeng
Li
(Wolfson Catalysis Centre, Department of Chemistry, University of Oxford)
,
Anna
Kroner
(Diamond Light Source)
,
Ziyan
Zeng
(Diamond Light Source)
,
Xinlin
Hong
(Diamond Light Source)
,
Youzhu
Yuan
(State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Production of Alcohols-Ethers-Esters, iChEM, College of Chemistry and Chemical Engineering, Xiamen University)
,
Xue-Qing
Gong
(Key Laboratory for Advanced Materials, Centre for Computational Chemistry and Research Institute of Industrial Catalysis, College of Chemistry and Molecular Engineering, East China University of Science and Technology)
Co-authored by industrial partner:
No
Type:
Journal Paper
Journal:
Green Chemistry
State:
Published (Approved)
Published:
October 2016
Abstract: At present, there is no low pressure methanol synthesis from CO2/H2 with high yield despite the presence of an upstream process of aqueous phase reforming (APR) of biomass derivatives at industrial scale for CO2/H2 production at ca. 2 MPa. This is due to the intrinsic thermodynamics of the system which leads to particularly high CO levels at low pressure through reversed water gas shift reaction (RWGS) for most studied catalysts. Here we report a new Pd@Zn core-shell catalyst that offers a significantly higher kinetic barrier for CO/H2O formation in CO2 hydrogenation to reduce the CO levels but facilitates CH3OH formation at or below 2 MPa with CH3OH selectivity maintained at ca. 70% comparing to ca. 10% over industrial Cu catalyst. The corresponding methanol yield at 2 MPa reaches 6.1 g methanol/g active metal *h which is comparable with the best reported value among a wide variety of catalysts under 5 MPa. It is thus, believed this active Pd based catalyst opens up a promising possibility for low pressure and temperature methanol production using renewable biomass resource for fossil-fuels-starved countries.
Diamond Keywords: Biofuel
Subject Areas:
Chemistry,
Energy,
Environment
Instruments:
B18-Core EXAFS
Added On:
11/11/2016 14:16
Discipline Tags:
Bioenergy
Earth Sciences & Environment
Sustainable Energy Systems
Energy
Climate Change
Physical Chemistry
Catalysis
Chemistry
Technical Tags:
Spectroscopy
X-ray Absorption Spectroscopy (XAS)
Extended X-ray Absorption Fine Structure (EXAFS)