甲醇
催化作用
结晶度
选择性
无机化学
制氢
傅里叶变换红外光谱
金属
氢
材料科学
核化学
化学
化学工程
有机化学
工程类
复合材料
作者
Zama G. Duma,John Moma,Henrietta W. Langmi,Benoît Louis,Ksenia Parkhomenko,Nicholas M. Musyoka
出处
期刊:Catalysts
[MDPI AG]
日期:2022-09-24
卷期号:12 (10): 1104-1104
被引量:3
标识
DOI:10.3390/catal12101104
摘要
Green methanol is a viable alternative for the storage of hydrogen and may be produced from captured anthropogenic sources of carbon dioxide. The latter was hydrogenated over Cu-ZnO catalysts supported on an aluminum fumarate metal-organic framework (AlFum MOF). The catalysts, prepared via slurry phase impregnation, were assessed for thermocatalytic hydrogenation of CO2 to methanol. PXRD, FTIR, and SBET exhibited a decrease in crystallinity of the AlFum MOF support after impregnation with Cu-Zn active sites. SEM, SEM-EDS, and TEM revealed that the morphology of the support is preserved after metal loading, where H2-TPR confirmed the presence of active sites for hydrogen uptake. The catalysts exhibited good activity, with a doubling in Cu and Zn loading over the AlFum MOF, resulting in a 4-fold increase in CO2 conversions from 10.8% to 45.6% and an increase in methanol productivity from 34.4 to 56.5 gMeOH/Kgcat/h. The catalysts exhibited comparatively high CO selectivity and high yields of H2O, thereby favoring the reverse water-gas shift reaction. The selectivity of the catalysts towards methanol was found to be 12.9% and 6.9%. The performance of the catalyst supported on AlFum MOF further highlights the potential use of MOFs as supports in the heterogeneous thermocatalytic conversion of CO2 to value-added products.
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