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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.
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页码:9153 / 9158
页数:6
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