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 cata...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2008-01, Vol.78 (1-2), p.73-79 |
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creator | Peluso, Miguel A. Pronsato, Estela Sambeth, Jorge E. Thomas, Horacio J. Busca, Guido |
description | 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 80h. 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. |
doi_str_mv | 10.1016/j.apcatb.2007.09.002 |
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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.</description><subject>Cryptomelane</subject><subject>Ethanol oxidation</subject><subject>FTIR</subject><subject>Indexing in process</subject><subject>Manganese oxide</subject><subject>Q1</subject><subject>VOCs</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkE1P4zAQhq0VK20p_AMOPnFL1l-NHQ5IqIIFAVppBWfLtSfgKo2D7bD03-NSznAajeaZV3ofhE4oqSmhze91bUZr8qpmhMiatDUh7AeaUSV5xZXiB2hGWtZUnEv-Cx2mtCaF4EzN0NPSZNNvs7fYhs1qStmHAYcOQ342Q-hx2cYpAjaDw6afNn4wOE3jGGIGh2-r-0K_eQfpDF8M-ObfB9j14T-OYGwOEac8ue0R-tmZPsHx55yjx6vLh-V1dff3z83y4q6ygopcceeElNBx4Ri1VnVOKFMqNp3lK96WAqRRzPAG7KIcpCBKCqlYwwWwwvA5Ot3njjG8TJCy3vhkoe_NAGFKmlPJWrFYfAvSVhS3cpco9qCNIaUInR6j35i41ZTonX691nv9eqdfk1bv5M7R-f4NSttXD1En62Gw4HwEm7UL_uuAd4S_j1A</recordid><startdate>20080117</startdate><enddate>20080117</enddate><creator>Peluso, Miguel A.</creator><creator>Pronsato, Estela</creator><creator>Sambeth, Jorge E.</creator><creator>Thomas, Horacio J.</creator><creator>Busca, Guido</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope></search><sort><creationdate>20080117</creationdate><title>Catalytic combustion of ethanol on pure and alumina supported K-Mn oxides: An IR and flow reactor study</title><author>Peluso, Miguel A. ; Pronsato, Estela ; Sambeth, Jorge E. ; Thomas, Horacio J. ; Busca, Guido</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-3dd477ef34d21cc8fd48a0166fc3b393370682a36ec58a0740874782634e2fc33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Cryptomelane</topic><topic>Ethanol oxidation</topic><topic>FTIR</topic><topic>Indexing in process</topic><topic>Manganese oxide</topic><topic>Q1</topic><topic>VOCs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peluso, Miguel A.</creatorcontrib><creatorcontrib>Pronsato, Estela</creatorcontrib><creatorcontrib>Sambeth, Jorge E.</creatorcontrib><creatorcontrib>Thomas, Horacio J.</creatorcontrib><creatorcontrib>Busca, Guido</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied catalysis. 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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 80h. 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.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2007.09.002</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cryptomelane Ethanol oxidation FTIR Indexing in process Manganese oxide Q1 VOCs |
title | Catalytic combustion of ethanol on pure and alumina supported K-Mn oxides: An IR and flow reactor study |
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