Ethanol auto-thermal reforming on rhodium catalysts and initial steps simulation on single crystals under UHV conditions

Autor: Erik Vesselli, Giovanni Comelli, Francesco Frusteri, Stefano Cavallaro, Renzo Rosei, S. Freni
Přispěvatelé: Vesselli, Erik, Comelli, Giovanni, Rosei, Renzo, Freni, S., Frusteri, F., Cavallaro, S.
Rok vydání: 2005
Předmět:
Zdroj: Applied catalysis. A, General
281 (2005): 139–147. doi:10.1016/j.apcata.2004.11.020
info:cnr-pdr/source/autori:E. Vesselli; G. Comelli; R. Rosei; S. FRENI; F. Frusteri; S. Cavallaro/titolo:Ethanol auto-thermal reforming on rhodium catalysts and initial steps simulation on single crystals under UHV conditions/doi:10.1016%2Fj.apcata.2004.11.020/rivista:Applied catalysis. A, General (Print)/anno:2005/pagina_da:139/pagina_a:147/intervallo_pagine:139–147/volume:281
ISSN: 0926-860X
Popis: By means of ultra high vacuum temperature programmed desorption experiments, we studied the influence of oxygen on the decomposition of ethanol over rhodium(1 1 1) and (1 0 0) single crystal surfaces. Oxygen at low surface coverage (between 0.1 and 0.25 ML) promotes ethanol decomposition and the formation of carbon dioxide, while carbon monoxide production is not significantly affected, with respect to the reaction on clean samples. Oxygen coverage above 0.25 ML hinders hydrogen formation due to the prevalent oxidising action, which leads to water formation. These results are in line with data we obtained for ethanol decomposition over a 5% Rh/Al 2 O 3 catalyst under typical reforming working conditions (i.e. T = 923 K and P = 1 bar), thus indicating that an oxidising environment is required in order to avoid carbon poisoning and to promote C 2 -containing molecules decomposition. On the contrary, excess of oxygen leads to a strong reduction of hydrogen concentration in the reaction products.
Databáze: OpenAIRE
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