Boosting light olefin selectivity in CO2 hydrogenation by adding Co to Fe catalysts within close proximity

被引:64
作者
Yuan, Fei [1 ]
Zhang, Guanghui [1 ]
Zhu, Jie [1 ]
Ding, Fanshu [1 ]
Zhang, Anfeng [1 ]
Song, Chunshan [1 ,2 ,3 ]
Guo, Xinwen [1 ]
机构
[1] Dalian Univ Technol, PSU DUT Joint Ctr Energy Res, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Penn State Univ, EMS Energy Inst, PSU DUT Joint Ctr Energy Res, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Energy & Mineral Engn & Chem Engn, University Pk, PA 16802 USA
基金
中国国家自然科学基金;
关键词
Fe-based catalysts; Lower olefin; CARBON-DIOXIDE HYDROGENATION; FISCHER-TROPSCH SYNTHESIS; HYDROCARBONS; CONVERSION; NANOPARTICLES; GENERATION; POTASSIUM; FERRITE; SURFACE; SODIUM;
D O I
10.1016/j.cattod.2020.07.072
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Direct conversion of carbon dioxide (CO2) into lower olefins (C2-C4=) is highly attractive as a sustainable production route for its great significance in greenhouse gas emission control and fossil fuel substitution. Fe-based catalysts have been extensively studied in CO2 hydrogenation, which usually show unsatisfactory selectivity toward lower olefins. Here we present a high-dispersion catalyst precursor CoFe2O4 with Na (Na-CoFe2O4) that offers C2-C4= space time yield as high as 2.88 mu molC2-C4= gcat 1 s-1 and olefin to paraffin ratio about 6 at CO2 conversion higher than 41 %. High dispersion and the intimate contact between Fe and Co sites help inhibit the formation of methane, and favor a higher selectivity of C2+ hydrocarbons, especially lower olefins. The presence of Na further promotes chain growth and suppresses the direct hydrogenation of Fe-(CH2)n intermediates. A superior stability over 100 h was observed, demonstrating the promising potential of this catalyst for industrial applications.
引用
收藏
页码:142 / 149
页数:8
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