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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/36359
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dc.contributor.authorSantos, L. P. S.-
dc.contributor.authorCamargo, E. R.-
dc.contributor.authorFabbro, M. T.-
dc.contributor.authorLongo, Elson-
dc.contributor.authorLeite, E. R.-
dc.date.accessioned2014-05-20T15:26:09Z-
dc.date.accessioned2016-10-25T18:00:42Z-
dc.date.available2014-05-20T15:26:09Z-
dc.date.available2016-10-25T18:00:42Z-
dc.date.issued2007-01-01-
dc.identifierhttp://dx.doi.org/10.1016/j.ceramint.2006.04.006-
dc.identifier.citationCeramics International. Oxford: Elsevier B.V., v. 33, n. 7, p. 1205-1209, 2007.-
dc.identifier.issn0272-8842-
dc.identifier.urihttp://hdl.handle.net/11449/36359-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/36359-
dc.description.abstractNanosized and highly reactive magnesium mobate (MgNb2O6) powders were successfully synthesized by a new wet-chemical method by means of the dissolution of Nb2O5 center dot 5H(2)O and in a solution of oxalic acid followed by the addition of stoichiometric amounts of magnesium carbonate. The Nb-Mg-oxalic acid solution was evaporated resulting in a dry and amorphous powder that was calcined in the temperature range from 200 to 900 degrees C for 2 h. The crystallization process from the amorphous state to the crystalline MgNb2O6 was followed by thermal analysis. The calcined powders characterized by FT-Raman spectroscopy, X-ray diffraction (XRD) and their morphology examined by high resolution scanning electron microscopy (HR-SEM). Pure MgNb2O6, free from the second phases and obtained at 800 degrees C was confirmed by a combined analysis using XRD and FT-Raman. The average diameter of the particles was calculated from the HR-SEM image as 70 urn approximately. This technique allows a better mixing of the constituent elements and thus a better reactivity of the mixture to obtain pre-reaction products with high purity at lower temperatures and reducing cost. It can offer a great advantage in the PMN-PT formation with respect to the solid-state synthesis. (c) 2006 Elsevier Ltd and Techna Group S.r.l. All rights reserved.en
dc.format.extent1205-1209-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectMgNb2O6pt
dc.subjectcolumbitept
dc.subjectmagnesium niobatept
dc.subjectlow temperature synthesispt
dc.subjectFT-Ramanpt
dc.titleWet-chemical synthesis of magnesium niobate nanoparticles powdersen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Fed Sao Carlos, Dept Quim, Lab Interdisciplinar Electroquim & Ceram, BR-13565905 Sao Carlos, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, Fac Ciências, BR-17033360 Bauru, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciências, BR-17033360 Bauru, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/j.ceramint.2006.04.006-
dc.identifier.wosWOS:000249191700010-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofCeramics International-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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