Tandem Reactions of CO2 Reduction and Ethane Aromatization

被引:98
作者
Gomez, Elaine [1 ]
Nie, Xiaowa [1 ,2 ]
Lee, Ji Hoon [1 ]
Xie, Zhenhua [3 ]
Chen, Jingguang G. [1 ,3 ]
机构
[1] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[2] Dalian Univ Technol, Sch Chem Engn, PSU DUT Joint Ctr Energy Res, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[3] Brookhaven Natl Lab, Div Chem, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; OXIDATIVE DEHYDROGENATION; CATALYTIC-CRACKING; CARBON-DIOXIDE; LIGHT OLEFINS; SOFT OXIDANT; HYDROCARBONS; CONVERSION; COMPLEXES; ZEOLITE;
D O I
10.1021/jacs.9b08538
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aromatization of light alkanes is of great interest because this can expand the raw materials used to produce aromatics to include fractions of natural gas that are readily available and inexpensive. Combining CO2 reduction with ethane dehydrogenation and aromatization can also mitigate CO, emissions. A one-step process that can produce liquid aromatics from the reactions of CO2 and ethane using phosphorus (P)- and gallium (Ga)-modified ZSM-5 has been evaluated at 873 K and atmospheric pressure. The addition of P improves the hydrothermal stability of Ga/ZSM-5, reduces coke formation on the catalyst surface, and allows the formation of more liquid aromatics through the tandem reactions of CO2-assisted oxidative dehydrogenation of ethane and subsequent aromatization. Density functional theory calculations provide insights into the effect of Ga- and P- modification on ethane dehydrogenation to ethylene as well as the role of CO2 on the production of aromatics.
引用
收藏
页码:17771 / 17782
页数:12
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