Catalytic combustion of ethanol on pure and alumina supported K-Mn oxides: An IR and flow reactor study

Mn-based catalysts prepared by oxidation of Mn(II) by KMnO4, pure and supported on alumina, calcined at 350 and 500 °C have been characterized and tested in the total oxidation of ethanol. IR experiments allowed us to have an indication on some aspects of the reaction mechanisms. The unsupported cat...

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Detalhes bibliográficos
Autores: Peluso, Miguel Andrés, Pronsato, Maria Estela, Sambeth, Jorge Enrique, Thomas, Horacio Jorge, Busca, Guido
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2008
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/51830
Acesso em linha:http://hdl.handle.net/11336/51830
Access Level:acceso abierto
Palavra-chave:Criptomelane
Manganese Oxide
Vocs
Ftir
Ethanol Oxidation
https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
Descrição
Resumo:Mn-based catalysts prepared by oxidation of Mn(II) by KMnO4, pure and supported on alumina, calcined at 350 and 500 °C have been characterized and tested in the total oxidation of ethanol. IR experiments allowed us to have an indication on some aspects of the reaction mechanisms. The unsupported catalysts calcined at 350 °C, mostly constituted by a cryptomelane phase were the most active, allowing the total conversion of ethanol at 180 °C, with excellent stability for at least 80 h. The reaction is initiated by the fast conversion of ethanol to acetate species via acetaldehyde. Later, the conversion of acetates to CO2 appears to be a slow step. On alumina-supported catalysts, which are (in spite of the much higher surface area) active only above 240 °C, part of acetate species are adsorbed on the support and act as inactive spectators.