HYDROGENATION OF SURFACE CARBON ON ALUMINA-SUPPORTED NICKEL

被引:357
|
作者
MCCARTY, JG
WISE, H
机构
[1] Solid-State Catalysis Laboratory, SRI International, Menlo Park
关键词
D O I
10.1016/0021-9517(79)90007-1
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
Four types of carbon were observed to form on an alumina-supported nickel methanation catalyst on exposure to carbon monoxide at 550 ± 50 K. In order of their reactivity toward hydrogen the carbon species may be classified as: chemisorbed carbon atoms (α), bulk nickel carbide, amorphous carbon (β), and crystalline elemental carbon. The α-phase and the initial monolayers of Ni3C are much more reactive than the elemental forms as measured by temperature-programmed surface reaction in 100 kPa H2. At 550 K the α- and β-carbon species formed by CO exposure populate the surface at a ratio of about 2:1. Both phases are relatively stable on heating to 600 K in a He atmosphere. At higher temperatures, slow conversion of α- and β-carbon to graphite was observed. Hydrogenation of the α state at 550 K leads to methane at a sufficiently fast rate to make it a likely intermediate in nickel-catalyzed methane synthesis from hydrogen and carbon monoxide. © 1979.
引用
收藏
页码:406 / 416
页数:11
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