Surface Carbon as a Reactive Intermediate in Dry Reforming of Methane to Syngas on a 5% Ni/MnO Catalyst

被引:75
作者
Gili, Albert [1 ]
Schlicker, Lukas [1 ]
Bekheet, Maged F. [1 ]
Goerke, Oliver [1 ]
Penner, Simon [2 ]
Gruenbacher, Matthias [2 ]
Goetsch, Thomas [2 ]
Littlewood, Patrick [3 ]
Marks, Tobin J. [3 ]
Stair, Peter C. [3 ]
Schomaecker, Reinhard [4 ]
Doran, Andrew [5 ]
Selve, Soeren [6 ]
Simon, Ulla [1 ]
Gurlo, Aleksander [1 ]
机构
[1] Tech Univ Berlin, Inst Werkstoffwissensch & Technol, Fachgebiet Keram Werkstoffe, Chair Adv Ceram Mat, Hardenbergstr 40, D-10623 Berlin, Germany
[2] Univ Innsbruck, Inst Phys Chem, Innrain 52c, A-6020 Innsbruck, Austria
[3] Northwestern Univ, Dept Chem, Ctr Catalysis & Surface Sci, 2145 Sheridan Rd, Evanston, IL 60208 USA
[4] Tech Univ Berlin, Inst Chem, Sekretariat TC 8,Str 17 Juni 124, D-10623 Berlin, Germany
[5] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
[6] Tech Univ Berlin, Ctr Electron Microscopy ZELMI, Str 17 Juni 135, D-10623 Berlin, Germany
基金
奥地利科学基金会;
关键词
carbon deposition; in situ XRD; synchrotron radiation; heterogeneous catalysis; DRM; nickel; surface carbon; NI NANOPARTICLES; SYNTHESIS GAS; SUPPORTED NI; NI/SIO2; CATALYST; PARTICLE-SIZE; CO2; CH4; DIOXIDE; PERFORMANCE; NANOTUBES;
D O I
10.1021/acscatal.8b01820
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
A 5% Ni/MnO catalyst has been tested for the dry reforming of methane at different temperatures and reactant partial pressures. Changing the reactant ratio with time on stream results in a decrease in the deactivation rate of the catalyst. Graphitic carbon growth and metal particle sintering have been observed by applying in situ transmission XRD using synchrotron radiation under actual reaction conditions. Both methane and carbon monoxide separately result in graphitic surface carbon, which can then be oxidized by carbon dioxide. The morphology of the surface carbon has been analyzed by TEM, and the reactions of both methane and carbon monoxide result in the same graphitic multiwalled carbon nanotubes. The present combination of catalytic experiments and in situ techniques suggests that surface carbon acts as an intermediate in the formation of CO and that catalyst deactivation happens via metallic particle sintering. These results enable a more rational choice of reaction conditions to ensure high catalyst activity and long-term stability. Future catalyst advances must aim to prevent metal particle sintering.
引用
收藏
页码:8739 / 8750
页数:23
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