Methanation of CO2: Structural response of a Ni-based catalyst under fluctuating reaction conditions unraveled by operando spectroscopy

被引:134
|
作者
Mutz, Benjamin [1 ,2 ]
Carvalho, Hudson W. P. [1 ]
Mangold, Stefan [3 ]
Kleist, Wolfgang [1 ,2 ]
Grunwaldt, Jan-Dierk [1 ,2 ]
机构
[1] Karlsruhe Inst Technol, Inst Chem Technol & Polymer Chem ITCP, D-76131 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Inst Catalysis Res & Technol IKFT, D-76344 Eggenstein Leopoldshafen, Germany
[3] Karlsruhe Inst Technol, Synchrotron Radiat Facil ANKA, D-76344 Eggenstein Leopoldshafen, Germany
关键词
Methanation; Carbon dioxide; Operando XAS; Dynamic reaction conditions; Ni catalyst; Deactivation; RAY-ABSORPTION SPECTROSCOPY; IN-SITU CHARACTERIZATION; CARBON-DIOXIDE; NI/AL2O3; CATALYSTS; HYDROGENATION;
D O I
10.1016/j.jcat.2015.04.006
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
The methanation of CO2 as a relevant strategy for energy storage has been studied by operando X-ray absorption spectroscopy under dynamic H-2/CO2 and CO2 reaction atmospheres. A typical CO2 conversion of 81% was reached at 400 degrees C with a 23 wt.-% Ni/CaO-Al2O3 catalyst, yielding 80% of CH4. The operando XAS experiment under working conditions revealed pronounced structural changes, e.g., a fast bulk oxidation of the Ni particles after removal of H-2 from the H-2/CO2 (4:1) gas stream. A lower performance of the catalyst was observed in the subsequent methanation cycle due to the presence of a residual oxidized fraction of Ni. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:48 / 53
页数:6
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