Study by thermogravimetry, electrical conductivity and IR spectrometry of the phase transition for manganese cation deficient spinels
Identifieur interne : 000D92 ( Istex/Corpus ); précédent : 000D91; suivant : 000D93Study by thermogravimetry, electrical conductivity and IR spectrometry of the phase transition for manganese cation deficient spinels
Auteurs : B. Gillot ; M. El Guendouzi ; M. Laarj ; P. Tailhades ; A. RoussetSource :
- Journal of Materials Science [ 0022-2461 ] ; 1988-09-01.
Abstract
Abstract: Thermogravimetry, electrical conductivity and IR spectrometry were used to study the crystal structure change of the metastable manganese cation deficient spinels that occur during the oxidation of manganese ions above 500° C. The kinetic of the transformation is found to be governed by a nucleation growth mechanism with an activation energy varying with the amount of Mn3+ ions. The nature of the inversion products depends on the manganese substitution extent. We observe for a substitution extent x<0.72 a phase with a corundum structure which is a solid solution of α-(MnFe)2O3 and for x>0.72 a mixture of two phases α-(MnFe)2O3 + Mn2O3 of orthorhombic structure.
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DOI: 10.1007/BF00551316
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<front><div type="abstract" xml:lang="en">Abstract: Thermogravimetry, electrical conductivity and IR spectrometry were used to study the crystal structure change of the metastable manganese cation deficient spinels that occur during the oxidation of manganese ions above 500° C. The kinetic of the transformation is found to be governed by a nucleation growth mechanism with an activation energy varying with the amount of Mn3+ ions. The nature of the inversion products depends on the manganese substitution extent. We observe for a substitution extent x<0.72 a phase with a corundum structure which is a solid solution of α-(MnFe)2O3 and for x>0.72 a mixture of two phases α-(MnFe)2O3 + Mn2O3 of orthorhombic structure.</div>
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<affiliation>Laboratoire de Chimie des Matériaux Inorganiques, Université Paul Sabatier, Toulouse III, 118 route de Narbonne, 31062, Toulouse Cedex, France</affiliation>
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<name type="personal"><namePart type="given">A.</namePart>
<namePart type="family">Rousset</namePart>
<affiliation>Laboratoire de Chimie des Matériaux Inorganiques, Université Paul Sabatier, Toulouse III, 118 route de Narbonne, 31062, Toulouse Cedex, France</affiliation>
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<originInfo><publisher>Kluwer Academic Publishers</publisher>
<place><placeTerm type="text">Dordrecht</placeTerm>
</place>
<dateCreated encoding="w3cdtf">1987-10-05</dateCreated>
<dateIssued encoding="w3cdtf">1988-09-01</dateIssued>
<copyrightDate encoding="w3cdtf">1988</copyrightDate>
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<language><languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract lang="en">Abstract: Thermogravimetry, electrical conductivity and IR spectrometry were used to study the crystal structure change of the metastable manganese cation deficient spinels that occur during the oxidation of manganese ions above 500° C. The kinetic of the transformation is found to be governed by a nucleation growth mechanism with an activation energy varying with the amount of Mn3+ ions. The nature of the inversion products depends on the manganese substitution extent. We observe for a substitution extent x<0.72 a phase with a corundum structure which is a solid solution of α-(MnFe)2O3 and for x>0.72 a mixture of two phases α-(MnFe)2O3 + Mn2O3 of orthorhombic structure.</abstract>
<relatedItem type="host"><titleInfo><title>Journal of Materials Science</title>
</titleInfo>
<titleInfo type="abbreviated"><title>J Mater Sci</title>
</titleInfo>
<genre type="journal" displayLabel="Archive Journal"></genre>
<originInfo><dateIssued encoding="w3cdtf">1988-09-01</dateIssued>
<copyrightDate encoding="w3cdtf">1988</copyrightDate>
</originInfo>
<subject><genre>Chemistry</genre>
<topic>Polymer Sciences</topic>
<topic>Industrial Chemistry/Chemical Engineering</topic>
<topic>Characterization and Evaluation Materials</topic>
<topic>Mechanics</topic>
</subject>
<identifier type="ISSN">0022-2461</identifier>
<identifier type="eISSN">1573-4803</identifier>
<identifier type="JournalID">10853</identifier>
<identifier type="IssueArticleCount">58</identifier>
<identifier type="VolumeIssueCount">12</identifier>
<part><date>1988</date>
<detail type="volume"><number>23</number>
<caption>vol.</caption>
</detail>
<detail type="issue"><number>9</number>
<caption>no.</caption>
</detail>
<extent unit="pages"><start>3342</start>
<end>3347</end>
</extent>
</part>
<recordInfo><recordOrigin>Chapman and Hall Ltd., 1988</recordOrigin>
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<identifier type="istex">58020309D601DBEB23FE497E54ACAC44B4663D4B</identifier>
<identifier type="DOI">10.1007/BF00551316</identifier>
<identifier type="ArticleID">BF00551316</identifier>
<identifier type="ArticleID">Art46</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Chapman and Hall Ltd, 1988</accessCondition>
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<recordOrigin>Chapman and Hall Ltd, 1988</recordOrigin>
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