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dc.contributor.authorWinatsara Kantanaen_US
dc.contributor.authorParkpoom Jarupoomen_US
dc.contributor.authorKamonpan Pengpaten_US
dc.contributor.authorSukum Eitssayeamen_US
dc.contributor.authorTawee Tunkasirien_US
dc.contributor.authorGobwute Rujijanagulen_US
dc.date.accessioned2018-09-04T09:23:43Z-
dc.date.available2018-09-04T09:23:43Z-
dc.date.issued2013-05-01en_US
dc.identifier.issn02728842en_US
dc.identifier.other2-s2.0-84875734858en_US
dc.identifier.other10.1016/j.ceramint.2012.10.098en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875734858&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52340-
dc.description.abstractEffects of zirconium oxide (ZrO2) nanoparticles additive on the microstructure and physical properties of hydroxyapatite (HA) were investigated. The HA powder was derived from natural bovine bone by a sequence of thermal processes. The composites containing nanoparticles of ZrO2(0.2-1.0 vol%) were fabricated by a solid-state reaction mixed oxide method. All samples showed traces of HA, beta-tricalcium phosphate (β-TCP) and alpha-tricalcium phosphate (α-TCP) phases while the x≥0.1 samples also showed ZrO2phase. Amount of β-TCP and α-TCP phases tend to decrease with ZrO2. The additive inhibited grain growth as a result of a decrease in grain size. However, the x=0.2 sample exhibited higher hardness value which is consistent with the density data. In addition, bioactivity test suggested that the additive promoted an apatite forming with the values of Ca/P close to the value obtained from HA. © 2013 Elsevier Ltd and Techna Group S.r.l.en_US
dc.subjectChemical Engineeringen_US
dc.subjectMaterials Scienceen_US
dc.titleProperties of hydroxyapatite/zirconium oxide nanocompositesen_US
dc.typeJournalen_US
article.title.sourcetitleCeramics Internationalen_US
article.volume39en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsRajamangala University of Technology Lannaen_US
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