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dc.contributor.advisorDonald R. Sadoway.en_US
dc.contributor.authorCooper, Benjamin Den_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Materials Science and Engineering.en_US
dc.date.accessioned2006-12-18T20:02:17Z
dc.date.available2006-12-18T20:02:17Z
dc.date.issued2006en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/35072
dc.descriptionThesis (S.B.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, June 2006.en_US
dc.description"May 2006."en_US
dc.descriptionIncludes bibliographical references (leaves 35-36).en_US
dc.description.abstractCarbon, tungsten, platinum, and iridium were examined as candidate anode materials for an electrolytic cell. The materials were pre-selected to endure high process temperatures and were characterized for inertness and high current density during electrolysis using voltammometric techniques. Inertness is viewable through current discrepancies dependent on voltage scan direction at low voltage, consumption of current by metal oxide formation, and ease of surface oxide electro-stripping. Conductivity during electrolytic oxidation is observable as current density maximization at high voltages. While carbon, tungsten, and platinum formed surface oxides, iridium remained quite inert. In addition, the voltage hold-time was found to affect the leading current density, as platinum performed best during cyclic voltammometry, but iridium performed best during potentiostatic electrolysis. The intermediate potentiodynamic scan-rate displays the transition from platinum to iridium dominated current density.en_US
dc.description.statementofresponsibilityby Benjamin D. Cooper.en_US
dc.format.extent36 leavesen_US
dc.format.extent1687097 bytes
dc.format.extent1686436 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypeapplication/pdf
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582
dc.subjectMaterials Science and Engineering.en_US
dc.titleElectrode materials for the electrolysis of metal oxidesen_US
dc.typeThesisen_US
dc.description.degreeS.B.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.oclc71231057en_US


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