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hal.structure.identifierUniversité du Québec à Trois-Rivières [UQTR]
dc.contributor.authorBIBIENNE, Thomas
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorRAZAFINDRAMANANA, Volatiana
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorBOBET, Jean-Louis
hal.structure.identifierUniversité du Québec à Trois-Rivières [UQTR]
dc.contributor.authorHUOT, Jacques
dc.date.issued2015
dc.identifier.issn0925-8388
dc.description.abstractEnThe morphology, crystal structure, and hydrogenation properties of the alloy 42Ti–21V–37Cr doped with 4 wt.% of Zr7Ni10 were investigated. Two doping schemes were used: (i) a single melt method, where all the components were melted together; (ii) a co-melt method where 42Ti–21V–37Cr alloy and Zr7Ni10 were first melted separately and thereafter re-melted together. The single melt alloy was a multi-phase compound, made of two intergranular phases within a Ti-, V-, Cr-rich matrix. One intergranular phase was Ti-, Zr-, Ni-rich and the other one Ti-rich. The co-melt alloy was a two phase material; a Ti-, V-, Cr-rich matrix and an homogeneously distributed Ti-, Zr-, Ni-rich intergranular phase.Both single melt and co-melt samples have a faster and more complete first hydrogenation (activation) than the undoped 42Ti–21V–37Cr. Activation is complete in less than 3 min for both doped alloys and their thermodynamics parameters are similar.
dc.language.isoen
dc.publisherElsevier
dc.subject.enHydrogen storage
dc.subject.enMetal hydrides
dc.subject.enBCC alloys
dc.subject.enZr7Ni10
dc.title.enSynthesis, characterization and hydrogen sorption properties of a Body Centered Cubic 42Ti–21V–37Cr alloy doped with Zr7Ni10
dc.typeArticle de revue
dc.identifier.doi10.1016/j.jallcom.2014.08.156
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Alloys and Compounds
bordeaux.page101-108
bordeaux.volume620
bordeaux.peerReviewedoui
hal.identifierhal-01086080
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01086080v1
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