Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/61672
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dc.contributor.authorWanwilai Chaisanen_US
dc.contributor.authorRattikorn Yimnirunen_US
dc.contributor.authorSupon Anantaen_US
dc.contributor.authorDavid P. Cannen_US
dc.date.accessioned2018-09-11T08:56:52Z-
dc.date.available2018-09-11T08:56:52Z-
dc.date.issued2006-08-15en_US
dc.identifier.issn09215107en_US
dc.identifier.other2-s2.0-33746645932en_US
dc.identifier.other10.1016/j.mseb.2006.04.033en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33746645932&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/61672-
dc.description.abstract(1-x)Pb(Zr0.52Ti0.48)O3-xBaTiO3ceramics were prepared by a modified mixed-oxide method. The phase formation was studied by XRD analysis. All compositions exhibit complete solid solutions of perovskite-like phase in the (1-x)PZT-xBT system. The (2 0 0)/(0 0 2) peak was found to split at the composition x = 0.6 and the co-existence of tetragonal-rhombohedral phases occurs with x ≤ 0.6. The possible range of compositions which correspond to a phase transition is 0.6 < x < 0.7. While pure BT ceramics exhibited a sharp phase transformation expected for normal ferroelectrics, phase transformation behavior of the (1-x)PZT-xBT solid solutions became more diffuse with increasing BT contents. This was primarily evidenced by an increased broadness in the dielectric peak, with a maximum peak width occurring at x = 0.5. © 2006 Elsevier B.V. All rights reserved.en_US
dc.subjectEngineeringen_US
dc.subjectMaterials Scienceen_US
dc.subjectPhysics and Astronomyen_US
dc.titlePhase development and dielectric properties of (1-x)Pb(Zr<inf>0.52</inf>Ti<inf>0.48</inf>)O<inf>3</inf>-xBaTiO<inf>3</inf>ceramicsen_US
dc.typeJournalen_US
article.title.sourcetitleMaterials Science and Engineering B: Solid-State Materials for Advanced Technologyen_US
article.volume132en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsOregon State Universityen_US
Appears in Collections:CMUL: Journal Articles

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