The activity and stability of catalysts for methane-carbon dioxide reforming depend subtly upon the support and the active metal. Methane decomposes to carbon and hydrogen, forming carbon on the oxide support and the metal. Carbon on the metal is reactive and can be oxidized to CO by oxygen from dissociatively adsorbed CO2. For noble metals this reaction is fast, leading to low coke accumulation on the metal particles. The rate of carbon formation on the support is proportional to the concentration of Lewis acid sites. This carbon is non reactive and may cover the Pt particles causing catalyst deactivation. Hence, the combination of Pt with a support low in acid sites, such as ZrO2 is well suited for long term stable operation. For non-noble metals such as Ni, the rate of CH4 dissociation exceeds the rate of oxidation drastically and carbon forms rapidly on the metal in the form of filaments. The rate of carbon filament formation is proportional to the particle size of Ni. Below a critical Ni particle, size (d<2 nm), formation of carbon slowed down dramatically. Well dispersed Ni supported on ZrO2 is thus a viable alternative to the noble metal based materials.
|Number of pages||12|
|Journal||Studies in surface science and catalysis|
|Publication status||Published - 1996|
|Event||11th International Congress On Catalysis, ICC 1996: 40th Anniversary - Baltimore, United States|
Duration: 30 Jun 1996 → 5 Jul 1996
Conference number: 11