Effect of Mn loading onto MnFeO nanocomposites for the CO2 hydrogenation reaction

被引:110
作者
Al-Dossary, M. [1 ]
Ismail, Adel A. [2 ,3 ]
Fierro, J. L. G. [1 ]
Bouzid, Houcine [2 ,4 ]
Al-Sayari, S. A. [2 ,5 ]
机构
[1] CSIC, Inst Catalysis & Petr Chem, E-28049 Madrid, Spain
[2] Najran Univ, Adv Mat & Nanores Ctr, PCSED, Najran 11001, Saudi Arabia
[3] CMRDI, Nanostruct Mat & Nanotechnol Div, Cairo 11421, Egypt
[4] Fac Sci Sfax, Lab Mat Ferroelect, Sfax 3018, Tunisia
[5] Najran Univ, Coll Sci & Artssharoura, Najran, Saudi Arabia
关键词
Fischer-Tropsch synthesis (FTS); CO2; hydrogenation; Mn promotion; Fe-based catalysts; Fe-based FTS catalysts; FISCHER-TROPSCH SYNTHESIS; MANGANESE OXIDE; SYNTHESIS CATALYSTS; CARBON-DIOXIDE; IRON CATALYST; LIGHT OLEFINS; PHASE; FE; HYDROCARBONS; NANOPARTICLES;
D O I
10.1016/j.apcatb.2014.10.064
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
This work describes the preparation of mesoporous xMnFe oxide (x = 0, 0.05, 0.1, 0.2, 0.3 and 0.5 molar ratios) nanocomposites through a one-step sol-gel process in the presence of a triblock copolymer as a structure-directing agent. The prepared oxides were used as catalysts in the CO2 hydrogenation via Fischer-Tropsch reactions for the production of valuable hydrocarbons. Among the catalysts, the 0.05MnFe catalyst performed best under the selected reaction conditions: a reaction temperature of 340 degrees C, overall pressure of 20 bar, reactant mixture of 23% CO2/69% H2/8% N-2 and flow rate of 20 mL min(-1). This catalyst provided a much higher conversion of CO2 to hydrocarbons (63.2% C-2-C-5, 3.9% to C6+ and 3.6% to oxygenates) and the lowest levels of CO and methane formation among the xMnFe series. Moreover, 0.05MnFe was the only catalyst with a mesoporous structure, and it had a substantially lower reduction temperature than did the other members of the series. The enhanced catalytic activity of the 0.05MnFe catalyst, which contains only a small amount of Mn, appears to result primarily from its high specific area and relatively easy reduction. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:651 / 660
页数:10
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