Monometallic iron catalysts with synergistic Na and S for higher alcohols synthesis via CO2 hydrogenation

被引:58
|
作者
Yao, Ruwei [1 ,2 ]
Wei, Jian [1 ]
Ge, Qingjie [1 ]
Xu, Jing [1 ,2 ]
Han, Yu [1 ,2 ]
Ma, Qingxiang [3 ]
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
[3] Ningxia Univ, State Key Lab Highefficiency Utilizat Coal & Gree, Yinchuan 750021, Ningxia, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; hydrogenation; Higher alcohols; Iron catalysts; Na-S synergy; CARBON-DIOXIDE HYDROGENATION; FISCHER-TROPSCH SYNTHESIS; SELECTIVE CONVERSION; ETHANOL SYNTHESIS; LOWER OLEFINS; SULFUR; PROMOTER; POTASSIUM; SYNGAS; OXIDATION;
D O I
10.1016/j.apcatb.2021.120556
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
Direct hydrogenation of CO2 to higher alcohols is highly attractive and challenging. Iron catalysts are generally not regarded as ideal candidates, owing to its poor ability for non-dissociative CO activation, and needs to combine with other metals (such as Rh, Pd, Cu) for above process. Herein, we proposed an iron catalyst comodified with Na and S (FeNaS-0.6), achieving a space-time yield of 80.5 mg g(cat)(-1) h(-1) for alcohols, more than 98 % of which corresponds to C2+ alcohols. The synergistic effects of Na and S enable the monometallic iron catalyst to provide matched molecularly adsorbed CO and alkyl species simultaneously required for higher alcohols synthesis. Sulfur existed in the form of sulfate, and its electron-withdrawing effects could transfrom the surrounding Fe sites for CO dissociation to those for non-dissociative CO adsorption. The DFT modeling also confirmed more facile formation of alcohols on the Na and S co-modified iron catalyst.
引用
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页数:10
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