共 22 条
Activation of supported nickel catalysts for carbon dioxide reforming of methane
被引:52
作者:

Souza, MD
论文数: 0 引用数: 0
h-index: 0
机构: Univ Fed Rio de Janeiro, COPPE, PEQ, NUCAT, BR-21945 Rio De Janeiro, Brazil

Clavé, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Fed Rio de Janeiro, COPPE, PEQ, NUCAT, BR-21945 Rio De Janeiro, Brazil

Dubois, V
论文数: 0 引用数: 0
h-index: 0
机构: Univ Fed Rio de Janeiro, COPPE, PEQ, NUCAT, BR-21945 Rio De Janeiro, Brazil

Perez, CAC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Fed Rio de Janeiro, COPPE, PEQ, NUCAT, BR-21945 Rio De Janeiro, Brazil

Schmal, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Fed Rio de Janeiro, COPPE, PEQ, NUCAT, BR-21945 Rio De Janeiro, Brazil
机构:
[1] Univ Fed Rio de Janeiro, COPPE, PEQ, NUCAT, BR-21945 Rio De Janeiro, Brazil
[2] Inst Meurice, B-1070 Brussels, Belgium
关键词:
methane;
syngas;
reforming;
nickel;
catalysts;
D O I:
10.1016/j.apcata.2004.05.026
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 new activation process was proposed for supported nickel catalysts in CO2 reforming of methane. The activation was performed by heating the catalyst up to 800degreesC under a mixture of CH4/O-2 = 2. Before activation the nickel catalysts present only nickel aluminate species; these species are partially reduced to metallic nickel during activation. SEM pictures showed formation of carbon filaments embedded with dispersed nickel particles, which are the active sites for methane reforming with CO2. The nickel loading and the support greatly influence the catalyst stability, the conversion increased with Ni loading on alumina support, while the promotion with zirconia did not improve the catalytic behavior. (C) 2004 Elsevier B.V. All rights reserved.
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页码:133 / 139
页数:7
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