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dc.contributor.authorAzubike, D.C.
dc.contributor.authorChrysanthou, A.
dc.contributor.authorTerry, B.S.
dc.date.accessioned2012-10-08T13:29:38Z
dc.date.available2012-10-08T13:29:38Z
dc.date.issued1994-06-01
dc.identifier.citationAzubike , D C , Chrysanthou , A & Terry , B S 1994 , ' Kinetic dissociation of nickel titanate and nickel tungstate in oxygen potential gradients ' , Journal of Materials Science , vol. 29 , no. 11 , pp. 2957-2962 . https://doi.org/10.1007/BF01117607
dc.identifier.issn0022-2461
dc.identifier.otherPURE: 1055176
dc.identifier.otherPURE UUID: 0b06e34b-49f7-4f90-a5f0-77bb8ab4f7cd
dc.identifier.otherScopus: 0028447197
dc.identifier.urihttp://hdl.handle.net/2299/9078
dc.descriptionCopyright 2007 Elsevier B.V., All rights reserved.
dc.description.abstractNickel titanate (NiTiO) and nickel tungstate (NiWO) were exposed to oxygen potential gradients at 1400 and 1100° C, and they were found to dissociate into their constituent oxides, namely, NiO and TiO, and WO and NiO, respectively. This is consistent with the non-equilibrium phenomenon of kinetic decomposition. In the case of nickel titanate, at the low-oxygen-potential side, TiO was formed as sharp needle-like structures within the titanate matrix, while at the high-oxygen-potential side, NiO was formed. In contrast, NiO was formed at the lower-oxygen-potential side in the case of nickel tungstate, while WO volatized off from the high-oxygen-potential side. This indicated that W diffuses faster than Ni in tungstates. In both cases, there were significant macroscopic shifts of the oxide with respect to the original position, established with Pt markers, towards the high-oxygen-potential sideen
dc.format.extent6
dc.language.isoeng
dc.relation.ispartofJournal of Materials Science
dc.titleKinetic dissociation of nickel titanate and nickel tungstate in oxygen potential gradientsen
dc.contributor.institutionCentre for Engineering Research
dc.contributor.institutionMaterials and Structures
dc.contributor.institutionSchool of Physics, Engineering & Computer Science
dc.contributor.institutionDepartment of Engineering and Technology
dc.contributor.institutionCentre for Climate Change Research (C3R)
dc.description.statusPeer reviewed
rioxxterms.versionofrecordhttps://doi.org/10.1007/BF01117607
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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