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DC Field | Value | Language |
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dc.contributor.author | Santos, L. P. S. | - |
dc.contributor.author | Camargo, E. R. | - |
dc.contributor.author | Fabbro, M. T. | - |
dc.contributor.author | Longo, Elson | - |
dc.contributor.author | Leite, E. R. | - |
dc.date.accessioned | 2014-05-20T15:26:09Z | - |
dc.date.accessioned | 2016-10-25T18:00:42Z | - |
dc.date.available | 2014-05-20T15:26:09Z | - |
dc.date.available | 2016-10-25T18:00:42Z | - |
dc.date.issued | 2007-01-01 | - |
dc.identifier | http://dx.doi.org/10.1016/j.ceramint.2006.04.006 | - |
dc.identifier.citation | Ceramics International. Oxford: Elsevier B.V., v. 33, n. 7, p. 1205-1209, 2007. | - |
dc.identifier.issn | 0272-8842 | - |
dc.identifier.uri | http://hdl.handle.net/11449/36359 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/36359 | - |
dc.description.abstract | Nanosized 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.extent | 1205-1209 | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier B.V. | - |
dc.source | Web of Science | - |
dc.subject | MgNb2O6 | pt |
dc.subject | columbite | pt |
dc.subject | magnesium niobate | pt |
dc.subject | low temperature synthesis | pt |
dc.subject | FT-Raman | pt |
dc.title | Wet-chemical synthesis of magnesium niobate nanoparticles powders | en |
dc.type | outro | - |
dc.contributor.institution | Universidade Federal de São Carlos (UFSCar) | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.description.affiliation | Univ Fed Sao Carlos, Dept Quim, Lab Interdisciplinar Electroquim & Ceram, BR-13565905 Sao Carlos, SP, Brazil | - |
dc.description.affiliation | Univ Estadual Paulista, Fac Ciências, BR-17033360 Bauru, SP, Brazil | - |
dc.description.affiliation | Univ Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil | - |
dc.description.affiliationUnesp | Univ Estadual Paulista, Fac Ciências, BR-17033360 Bauru, SP, Brazil | - |
dc.description.affiliationUnesp | Univ Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil | - |
dc.identifier.doi | 10.1016/j.ceramint.2006.04.006 | - |
dc.identifier.wos | WOS:000249191700010 | - |
dc.rights.accessRights | Acesso restrito | - |
dc.relation.ispartof | Ceramics International | - |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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