Catalyst design for natural-gas upgrading through oxybromination chemistry

被引:85
|
作者
Paunovic, Vladimir [1 ]
Zichittella, Guido [1 ]
Moser, Maximilian [1 ]
Amrute, Amol P. [1 ]
Perez-Ramirez, Javier [1 ]
机构
[1] ETH, Inst Chem & Bioengn, Dept Chem & Appl Biosci, Vladimir Prelog Weg 1, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
VANADYL PYROPHOSPHATE; SELECTIVE OXIDATION; SURFACE-ACIDITY; N-BUTANE; BROMINE; METHANE; ACTIVATION; TRANSFORMATION; CONDENSATION; HYDROCARBONS;
D O I
10.1038/nchem.2522
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Natural gas contains large volumes of light alkanes, and its abundant reserves make it an appealing feedstock for value-added chemicals and fuels. However, selectively activating the C-H bonds in these useful hydrocarbons is one of the greatest challenges in catalysis. Here we report an attractive oxybromination method for the one-step functionalization of methane under mild conditions that integrates gas-phase alkane bromination with heterogeneously catalysed HBr oxidation, a step that is usually executed separately. Catalyst-design strategies to provide optimal synergy between these two processes are discussed. Among many investigated material families, vanadium phosphate (VPO) is identified as the best oxybromination catalyst, as it provides selectivity for CH3Br up to 95% and stable operation for over 100 hours on stream. The outstanding performance of VPO is rationalized by its high activity in HBr oxidation and low propensity for methane and bromomethane oxidation. Data on the oxybromination of ethane and propane over VPO suggest that the reaction network for higher alkanes is more complex.
引用
收藏
页码:803 / 809
页数:7
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