Bifunctionality of Cu/ZnO catalysts for alcohol-assisted low-temperature methanol synthesis from syngas:Effect of copper content
Alcohol-assisted low-temperature methanol synthesis was conducted over Cu/ZnOX catalysts while varying the copper content(X). Unlike conventional methanol synthesis, ethanol acted as both solvent and reaction intermediate in this reaction, creating a different reaction pathway. The formation of crys...
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Published in | Journal of energy chemistry Vol. 26; no. 3; pp. 373 - 379 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.05.2017
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Subjects | |
Online Access | Get full text |
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Summary: | Alcohol-assisted low-temperature methanol synthesis was conducted over Cu/ZnOX catalysts while varying the copper content(X). Unlike conventional methanol synthesis, ethanol acted as both solvent and reaction intermediate in this reaction, creating a different reaction pathway. The formation of crystalline phases and characteristic morphology of the co-precipitated precursors during the co-precipitation step were important factors in obtaining an efficient Cu/ZnO catalyst with a high dispersion of metallic copper,which is one of the main active sites for methanol synthesis. The acidic properties of the Cu/ZnO catalyst were also revealed as important factors, since alcohol esterification is considered the rate-limiting step in alcohol-assisted low-temperature methanol synthesis. As a consequence, bifunctionality of the Cu/ZnO catalyst such as metallic copper and acidic properties was required for this reaction. In this respect, the copper content(X) strongly affected the catalytic activity of the Cu/ZnOX catalysts, and accordingly, the Cu/ZnO0.5 catalyst with a high copper dispersion and sufficient acid sites exhibited the best catalytic performance in this reaction. |
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Bibliography: | Ilho Kim;Gihoon Lee;Heondo Jeong;Jong Ho Park;Ji Chul Jung;Department of Chemical Engineering,Myongji University;Korea Institute of Energy Research 21-1585/O4 |
ISSN: | 2095-4956 |
DOI: | 10.1016/j.jechem.2017.02.003 |