合成气
催化作用
串联
化学
乙醇
二甲醚
羰基化
选择性
产量(工程)
吡啶
有机化学
一氧化碳
材料科学
冶金
复合材料
作者
Songyue Han,Dong Fan,Nan Chen,Wenhao Cui,Linhai He,Peng Tian,Zhongmin Liu
出处
期刊:ACS Catalysis
日期:2023-07-31
卷期号:13 (16): 10651-10660
被引量:11
标识
DOI:10.1021/acscatal.3c01577
摘要
Syngas conversion into ethanol by tandem catalysis has exhibited its potential for the selective production of ethanol. For practical applications, it is desired to develop a robust catalyst system to enhance the CO conversion while maintaining high selectivity to ethanol. Here, we report an efficient and stable triple-tandem catalyst system consisting of CuZnAlOx/γ-Al2O3, pyridine-modified H-MOR zeolite (Py-HMOR), and Cu1Zn2AlOx, which catalyzes syngas to dimethyl ether (DME), DME carbonylation to methyl acetate (MA), and MA hydrogenation to ethanol in tandem. Both high CO conversion (52%) and satisfying selectivity to ethanol (62%, excluding CO2) were achieved simultaneously, leading to an unprecedently high ethanol space-time yield of 6.5 mmol g–1 h–1. In situ DRIFT and control catalytic tests were designed to elucidate the intrinsic reason of the high activity and stability of Py-HMOR in the tandem system. The developed tandem catalyst system presents a promising prospect for the direct ethanol manufacture from syngas.
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