Use este identificador para citar ou linkar para este item: http://repositorio.ufc.br/handle/riufc/55882
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dc.contributor.authorSilva, Marcelo Antonio Santos da-
dc.contributor.authorFernandes, Tatiana Sainara Maia-
dc.contributor.authorSantiago, Alexander Arley Xavier-
dc.contributor.authorSales, Juscelino Chaves-
dc.contributor.authorSombra, Antônio Sérgio Bezerra-
dc.date.accessioned2020-12-30T20:40:35Z-
dc.date.available2020-12-30T20:40:35Z-
dc.date.issued2011-
dc.identifier.citationSILVA, Marcelo Antonio Santos da; FERNANDES, Tatiana Sainara Maia; SANTIAGO, Alexander Arley Xavier; SALES, Juscelino Chaves; SOMBRA, Antônio Sérgio Bezerra. Synthesis and caracterization of CTO (CaTiO3). In: CONGRESSO BRASILEIRO DE CERÂMICA, 55º, 29 maio a 01 jun. 2011, Porto de Galinhas, Pernambuco, Brasil. Anais[…] Porto de Galinhas, Pernambuco, 2011.pt_BR
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/55882-
dc.description.abstractThe objective of this work is to study the ceramic material CTO (CaTiO3) by X-Ray Diffraction. The composites of CTO are widely used in dielectric resonators in communication systems. The CTO was prepared by solid state method in a planetary high energy ball milling (Fritsch Pulverisette 5). Stoichiometric quantities of CaCO3 (Aldrich 99%) and TiO2 (Merck 99%) were dry milled during 4h with a rotational speed of 370 rpm and then calcined at 1000 ºC for 3h. After, the CTO was studied by X-ray diffraction (XRD). The refinament showed that the CTO was formed with 100% mass, the graph of Williamson-Hall showed a homogeneous sample, with a contraction in the crystal lattice and a reasonably small particle size.pt_BR
dc.language.isoenpt_BR
dc.subjectMétodo de sinestesia no estado sólidopt_BR
dc.subjectDifração de raios - Xpt_BR
dc.subjectRefinamentopt_BR
dc.titleSynthesis and caracterization of CTO (CaTiO3)pt_BR
dc.typeArtigo de Eventopt_BR
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