Oxidation of Ethanol and Carbon Monoxide on Alumina-Supported Metal/Metal Oxide Xerogel Catalysts

dc.contributor.advisor Şeker, Erol
dc.contributor.author Ateş, Selcan
dc.date.accessioned 2014-07-22T13:51:02Z
dc.date.available 2014-07-22T13:51:02Z
dc.date.issued 2011
dc.description Thesis (Master)--Izmir Institute of Technology, Chemical Engineering, Izmir, 2011 en_US
dc.description Includes bibliographical references (leaves: 49-53) en_US
dc.description Text in English; Abstract: Turkish and English en_US
dc.description ix, 58 leaves en_US
dc.description.abstract The main goal of the study is to investigate the effect of metal type, metal oxide type and metal/oxide loading on the conversion as a function of temperature for the complete combustion of ethanol and CO in air over single step sol-gel made Al2O3 supported metal and mixed metal oxides. Two types of catalysts, Pt/Al2O3 (1, 2, and 3 % Pt loaded) and CuO-Mn2O3/Al2O3, with Cu/Mn molar ratio of 1:1, 5:1 and 12:1, and 50, 70, and 90% metal loading, were synthesized by impregnation and single step sol-gel methods, respectively. In addition, by synthesizing CuO/Al2O3, Mn2O3/Al2O3 and Pd-Mn2O3/Al2O3, the catalytic activity relationship between metal and metal oxides were clarified. Characterization of the samples was performed by XRD, BET, and FT-IR techniques and it was observed that among the metal oxide catalysts, CuO-Mn2O3/Al2O3 (70 wt%; (Cu/Mn)molar=1) showed the highest activity due to the formation of Cu1.5Mn1.5O4 phase while 3% Pt loaded alumina was the catalyst demonstrated the highest catalytic activity among the noble metal catalysts. Also, Pd addition enhanced the activity of metal oxide catalyst by lowering the temperature at which ~99% ethanol conversion was obtained. Moreover, deactivation of CuO-Mn2O3/Al2O3 mixed oxides was observed due to the irreversible adsorption of CO2 on catalyst surface at low temperatures. Except for Pt containing catalysts, the catalysts that showed high catalytic activity in ethanol oxidation was also tested for CO oxidation and CO2 formation was detected qualitatively at varying operating temperatures. en_US
dc.identifier.uri https://hdl.handle.net/11147/3178
dc.language.iso en en_US
dc.publisher Izmir Institute of Technology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject.lcsh Ethanol en
dc.subject.lcsh Carbon monoxide en
dc.subject.lcsh Aluminum oxide en
dc.subject.lcsh Oxidation en
dc.subject.lcsh Catalysts en
dc.title Oxidation of Ethanol and Carbon Monoxide on Alumina-Supported Metal/Metal Oxide Xerogel Catalysts en_US
dc.type Master Thesis en_US
dspace.entity.type Publication
gdc.author.institutional Ateş, Selcan
gdc.coar.access open access
gdc.coar.type text::thesis::master thesis
gdc.description.department Thesis (Master)--İzmir Institute of Technology, Chemical Engineering en_US
gdc.description.publicationcategory Tez en_US
gdc.description.scopusquality N/A
gdc.description.wosquality N/A
relation.isAuthorOfPublication.latestForDiscovery 9cd609c1-0abd-471c-bc86-0a3b835c3120
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4021-8abe-a4dfe192da5e

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