<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-18T21:58:07Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/115607" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/115607</identifier><datestamp>2026-06-17T14:46:57Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Antoine Allanore.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Nakanishi, Bradley Rex</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department of Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2018-05-23T15:04:25Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2018-05-23T15:04:25Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2018</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2018</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/115607</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1036986491</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2018.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">This electronic version was submitted by the student author.  The certified thesis is available in the Institute Archives and Special Collections.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from student-submitted PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The electrolytic cell method and its application for Gibbs energy measurement in high temperature, concentrated ionic melts was investigated. Previous challenges related primarily to signal interpretation during decomposition voltage measurement have hindered determination of Gibbs energy. An electrolytic cell method is proposed herein utilizing the sensitivity of large amplitude alternating current voltammetry, which enabled precise measurement of chemical potential during electrolytic decomposition. A novel, containerless approach for electrochemical study of high temperature, reactive electrolytes in a molten pendant droplet is described. For the first time, melts of pure alumina, lanthana and yttria were electrolytically decomposed to metal alloy and oxygen gas using iridium electrodes. The method was validated in molten alumina. Systematic investigation of the half-cell reactions corresponding to oxygen evolution and aluminum deposition revealed their electrochemical nature. Measurements of the chemical potential and partial molar entropy of aluminum in an iridium-rich, binary alloy liquid were obtained in close agreement with previous predictions. The method was extended to the pseudo-binary system molten lanthana-yttria. The results revealed selective extraction of lanthanum and indicated that molten lanthana-yttria does not exhibit ideal mixing behavior, contradicting previous predictions. However, data interpretation in multicomponent electrolyte compositions were challenged primarily by a lack of thermodynamic data for the attendant alloy system and influence of dissolved oxygen on the observed alloy composition. This work represents a pioneering effort for electrochemical operation in molten refractory oxides at temperatures above 2000 K.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Bradley Rex Nakanishi.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">205 pages</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">On the electrolytic nature of molten aluminum and rare earth oxides</dim:field>
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   	&lt;Title>On the electrolytic nature of molten aluminum and rare earth oxides&lt;/Title>
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   	&lt;PublicationDate>2018&lt;/PublicationDate>
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        	&lt;DisplayName>Nakanishi, Bradley Rex&lt;/DisplayName>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>The electrolytic cell method and its application for Gibbs energy measurement in high temperature, concentrated ionic melts was investigated. Previous challenges related primarily to signal interpretation during decomposition voltage measurement have hindered determination of Gibbs energy. An electrolytic cell method is proposed herein utilizing the sensitivity of large amplitude alternating current voltammetry, which enabled precise measurement of chemical potential during electrolytic decomposition. A novel, containerless approach for electrochemical study of high temperature, reactive electrolytes in a molten pendant droplet is described. For the first time, melts of pure alumina, lanthana and yttria were electrolytically decomposed to metal alloy and oxygen gas using iridium electrodes. The method was validated in molten alumina. Systematic investigation of the half-cell reactions corresponding to oxygen evolution and aluminum deposition revealed their electrochemical nature. Measurements of the chemical potential and partial molar entropy of aluminum in an iridium-rich, binary alloy liquid were obtained in close agreement with previous predictions. The method was extended to the pseudo-binary system molten lanthana-yttria. The results revealed selective extraction of lanthanum and indicated that molten lanthana-yttria does not exhibit ideal mixing behavior, contradicting previous predictions. However, data interpretation in multicomponent electrolyte compositions were challenged primarily by a lack of thermodynamic data for the attendant alloy system and influence of dissolved oxygen on the observed alloy composition. This work represents a pioneering effort for electrochemical operation in molten refractory oxides at temperatures above 2000 K.&lt;/Abstract>
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