Highly Selective Conversion of Carbon Dioxide to Lower Olefins

被引:484
|
作者
Li, Zelong [1 ]
Wang, Jijie [1 ]
Qu, Yuanzhi [1 ]
Liu, Hailong [1 ]
Tang, Chizhou [1 ]
Miao, Shu [1 ]
Feng, Zhaochi [1 ]
An, Hongyu [1 ]
Li, Can [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
来源
ACS CATALYSIS | 2017年 / 7卷 / 12期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
tandem catalysis; CO2; hydrogenation; C-C coupling; thermodynamic coupling; solid solution oxide; METAL-ORGANIC FRAMEWORKS; CO2; HYDROGENATION; METHANOL SYNTHESIS; BIFUNCTIONAL CATALYSTS; HYDROCARBON SYNTHESIS; PRODUCT SELECTIVITY; HYBRID CATALYSTS; LIGHT OLEFINS; SYNTHESIS GAS; SYNGAS;
D O I
10.1021/acscatal.7b03251
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
Conversion of CO2 to value-added chemicals has been a long-standing objective, and direct hydrogenation of CO2 to lower olefins is highly desirable but still challenging. Herein, we report a selective conversion of CO2 to lower olefins through CO2 hydrogenation over a ZnZrO/SAPO tandem catalyst fabricated with a ZnO-ZrO, solid solution and a Zn-modified SAPO-34 zeolite, which can achieve a selectivity for lower olefins as high as 80-90% among hydrocarbon products. This is realized on the basis of the dual functions of the tandem catalyst: hydrogenation of CO2 on the ZnO-ZrO2, solid solution and lower olefins production on the SAPO zeolite. The thermodynamic and kinetic coupling between the tandem reactions enable the highly efficient conversion of CO2 to lower olefins. Furthermore, this catalyst is stable toward the thermal and sulfur treatments, showing the potential industrial application.
引用
收藏
页码:8544 / 8548
页数:5
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