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dc.contributor.authorGonzález, Francisco-
dc.contributor.authorMunuera, Guillermo-
dc.contributor.authorPrieto, Juan A.-
dc.date.accessioned2025-04-12T04:36:10Z-
dc.date.available2025-04-12T04:36:10Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18651-
dc.description.abstractThe interaction of CH3COOH with anatase TiO2 surfaces has been studied and the results analysed in connection with those previously obtained for HCOOH on this and other oxides. The electron-donor properties of the carboxylate species formed at the surface were found to enhance the thermal elimination of surface hydroxyls, thus determining the actual state of the surface under catalytic conditions. Formation of ketene was detected by i.r.; a mechanism, involving this ketene and molecularly adsorbed acid in equilibrium with the gas phase, has been put forward for catalytic ketonization on TiO2 at T < 350°C. Decomposition of the adsorbed acetate at T > 350°C in the absence of gas phase produces alkyl-metal species (Ti—CH3) which, at T > 400°C, give C2H6 and CH4 leading to irreversible coke poisoning of the surface.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (06)en_US
dc.subjectChemistryen_US
dc.subjectKetonization reactionen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleMechanism of ketonization of acetic acid on anatase TiO2 surfacesen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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