Ozone Decomposition and Acetone Oxidation on Manganese Oxide Catalysts

dc.contributor.authorXi, Yanen
dc.contributor.committeechairOyama, Shigeo Teden
dc.contributor.committeememberCox, David F.en
dc.contributor.committeememberHanson, Brian E.en
dc.contributor.departmentChemical Engineeringen
dc.date.accessioned2014-03-14T20:38:10Zen
dc.date.adate2005-06-15en
dc.date.available2014-03-14T20:38:10Zen
dc.date.issued2005-05-11en
dc.date.rdate2005-06-15en
dc.date.sdate2005-05-22en
dc.description.abstractThis thesis describes the preparation and characterization of manganese oxide catalysts and their application in the oxidation of acetone, a typical volatile organic compound (VOC), and ozone decomposition. This topic is of great value because of environmental concerns of the elimination of the harmful VOCs and ozone. Manganese oxide was chosen because it is a well-known complete oxidation catalyst for VOCs and also an active catalyst for ozone decomposition. Two cases of studies were carried out in this work. The first study involved the oxidation of acetone using ozone on silica- and alumina-supported manganese oxide catalysts deposited on aluminum oxide foam substrates. The characteristics of the catalysts were determined through various techniques, including x-ray diffraction (XRD), x-ray absorption spectroscopy (XAS), Brunauer-Emmett-Teller (BET) surface area analysis, temperature-programmed reduction (TPR), and oxygen chemisorption. The use of these techniques allowed better understanding of the nature of the catalysts. Activity tests were carried out in the acetone oxidation reaction and it was found that the usage of ozone substantially reduced the oxidation temperature. Steady-state in situ Raman spectroscopy was also carried out to better understand the mechanism of the acetone oxidation reaction using ozone. The second study involved an investigation of structural and electronic properties of manganese centers of the MnOx/SiO2 and MnOx/Al2O3 catalysts during the ozone decomposition reaction using in situ x-ray absorption spectroscopy (XAS). The number of surface active sites was again determined through TPR and oxygen chemisorption measurements. The performance of the catalysts with different loadings and supports were also compared.en
dc.description.degreeMaster of Scienceen
dc.identifier.otheretd-05222005-141806en
dc.identifier.sourceurlhttp://scholar.lib.vt.edu/theses/available/etd-05222005-141806/en
dc.identifier.urihttp://hdl.handle.net/10919/33112en
dc.publisherVirginia Techen
dc.relation.haspartChapter4.pdfen
dc.relation.haspartVita.pdfen
dc.relation.haspartChapter3_corrected.pdfen
dc.relation.haspartAbstract.pdfen
dc.relation.haspartTable_of_Contents.pdfen
dc.relation.haspartChapter1.pdfen
dc.relation.haspartAcknowledgements.pdfen
dc.relation.haspartTitle_Page_corrected.pdfen
dc.relation.haspartChapter2_corrected.pdfen
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subjectManganese oxide catalystsen
dc.subjectVOCsen
dc.subjectozoneen
dc.subjectacetoneen
dc.subjectfoamen
dc.subjectX-ray absorption spectroscopyen
dc.titleOzone Decomposition and Acetone Oxidation on Manganese Oxide Catalystsen
dc.typeThesisen
thesis.degree.disciplineChemical Engineeringen
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.levelmastersen
thesis.degree.nameMaster of Scienceen

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