Hydrogen production through CO2 reforming of methane over Ni/CeZrO2/Al2O3 catalysts

被引:58
|
作者
Faria, E. C. [1 ,2 ]
Neto, R. C. R. [2 ]
Colman, R. C. [1 ]
Noronha, F. B. [2 ]
机构
[1] Univ Fed Fluminense, BR-24210240 Niteroi, RJ, Brazil
[2] Inst Nacl Tecnol, BR-20081310 Rio De Janeiro, Brazil
关键词
CO2 reforming of methane; Ni/CexZr1-xO2; /Al2O3; catalysts; Hydrogen; production; Gas-to-liquid technology; SUPPORTED CERIA-ZIRCONIA; PARTIAL OXIDATION; PT/CEZRO2/AL2O3; CATALYSTS; OXYGEN STORAGE; CARBON-DIOXIDE; MIXED-OXIDE; CH4; ALUMINA; PT/ZRO2; METALS;
D O I
10.1016/j.cattod.2013.10.058
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This work studied the performance of Ni/CexZr1-xO2/Al2O3 (x = 0.5; 0.75; 1.0) catalysts for the production of synthesis gas through CO2 reforming of CH4. Ni/Al2O3 and Ni/CeO2/Al2O3 catalysts exhibited an increase of methane and CO2 conversion at the beginning of reaction. For Ni/Ce0.75Zr0.25O2/Al2O3 and Ni/Ce-0.50 Zr0.50O2/Al2O3 catalysts, the conversion remained quite constant during the reaction. This result was associated with the oxidation of metallic Ni particles by CO2 from the feed. Ceria-zirconia support was preferentially oxidized, inhibiting the oxidation of the metallic phase. Carbon was formed over all catalysts. However, the amount of carbon deposits significantly decreased for Ni/Ce0.75Zr0.25O2/Al2O3 and Ni/Ce0.50Zr0.50O2/Al2O3 catalysts. This result was attributed to the high oxygen mobility of the homogeneous solid solution formed, which promoted the mechanism of carbon removal from the metallic particle. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 144
页数:7
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