Cascade Catalysis for the Hydrogenation of Carbon Dioxide to Methyl Formate Using a Molecular Ru-Phosphine Complex and the Metal-Organic Framework UiO-66 as Heterogeneous Acid

被引:4
作者
Lemmens, Vincent [1 ]
Vanbergen, Thomas [1 ]
O'Rourke, Galahad [1 ]
Marquez, Carlos [1 ]
De Vos, Dirk E. [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Membrane Separat Adsorpt Catalysis & Spect Sus, B-3001 Leuven, Belgium
关键词
cascade catalysis; CO2; methyl formate; metal-organic framework; UiO-66; IN-SITU HYDROGENATION; CO2; CAPTURE; HOMOGENEOUS HYDROGENATION; INTEGRATED PROCESS; METHANOL; PRESSURE; SALTS; AMINE; WATER;
D O I
10.1021/acsaem.2c03856
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The direct incorporation of CO2 into value-added base chemicals, such as methyl formate (MF), is a grand challenge to chemical science. In this work, a base-free cascade catalysis system is described to effectively convert carbon dioxide into MF. In the initial step a well-established Ru complex (i.e., RuHCl(dppm)2, dppm = 1,1-bis(diphenylphosphino)methane) is able to hydrogenate CO2 into formic acid, which subsequently undergoes a heterogeneous acid catalyzed esterification with methanol to selectively produce MF. Here, the small pore MOF UiO-66, a Zr-terephthalate, is identified as a promising heterogeneous acid and its Zr6 cluster is modified to understand the effect of Bronsted/Lewis acidity on the performance. Moreover, this heterogeneous acid catalyst could be reused for multiple times without significantly losing its activity.
引用
收藏
页码:9153 / 9158
页数:6
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