Directly converting CO2 into a gasoline fuel

被引:893
作者
Wei, Jian [1 ,2 ]
Ge, Qingjie [1 ]
Yao, Ruwei [1 ,2 ]
Wen, Zhiyong [1 ,2 ]
Fang, Chuanyan [1 ]
Guo, Lisheng [1 ,2 ]
Xu, Hengyong [1 ]
Sun, Jian [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
CARBON-DIOXIDE REDUCTION; FISCHER-TROPSCH SYNTHESIS; SELECTIVE CONVERSION; METHANOL SYNTHESIS; LOWER OLEFINS; LIGHT OLEFINS; CATALYSTS; HYDROGENATION; IRON; ZEOLITE;
D O I
10.1038/ncomms15174
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The direct production of liquid fuels from CO2 hydrogenation has attracted enormous interest for its significant roles in mitigating CO2 emissions and reducing dependence on petrochemicals. Here we report a highly efficient, stable and multifunctional Na-Fe3O4/HZSM-5 catalyst, which can directly convert CO2 to gasoline-range (C-5-C-11) hydrocarbons with selectivity up to 78% of all hydrocarbons while only 4% methane at a CO2 conversion of 22% under industrial relevant conditions. It is achieved by a multifunctional catalyst providing three types of active sites (Fe3O4, Fe5C2 and acid sites), which cooperatively catalyse a tandem reaction. More significantly, the appropriate proximity of three types of active sites plays a crucial role in the successive and synergetic catalytic conversion of CO2 to gasoline. The multifunctional catalyst, exhibiting a remarkable stability for 1,000 h on stream, definitely has the potential to be a promising industrial catalyst for CO2 utilization to liquid fuels.
引用
收藏
页数:8
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