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dc.contributor.authorPinto, Luiz Carlos Barbosa de Miranda-
dc.contributor.authorRighi, Ariete-
dc.contributor.authorLameiras, Fernando Soares-
dc.contributor.authorAraújo, Fernando Gabriel da Silva-
dc.contributor.authorKrambrock, Klaus Wilhelm Heinrich-
dc.date.accessioned2017-03-08T16:03:10Z-
dc.date.available2017-03-08T16:03:10Z-
dc.date.issued2011-
dc.identifier.citationPINTO, L. C. B. de M. et al. Origin of the color in cobalt-doped quartz. Physics and Chemistry of Minerals, v. 38, p. 623-629, 2011. Disponível em: <https://link.springer.com/article/10.1007/s00269-011-0434-3>. Acesso em: 08 mar. 2017.pt_BR
dc.identifier.issn1432-2021-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/7338-
dc.description.abstractSynthetic Co-doped quartz was grown hydrothermally in steel autoclaves at the Technological Center of Minas Gerais (CETEC), Brazil. The quartz samples, originally yellow in the as-grown state acquired blue coloration after prolonged heat treatment times at 500°C near the alpha–beta transition temperature. UV–VIS–NIR absorption spectroscopy shows the characteristic spectra of Co3+ before heat treatment. After heat treatment, the optical absorption spectrum is dominated by two split-triplet bands the Wrst in the near infrared region centered at about 6,700 cm¡1 (1,490 nm) and the second in the visible spectral range at about 16,900 cm¡1 (590 nm). Both split-triplet bands are typical for Co2+ ions in tetrahedral coordination environments. From the absence of electron paramagnetic resonance (EPR) spectra, we conclude that the Co2+ found in the optical absorption spectra of the blue quartz is not due to an isolated structural site in the quartz lattice. Instead, the blue color is associated with electronic transitions of Co2+ in small inclusions in which the Co site has tetrahedral symmetry. The non-observation of polarizationdepend optical absorption spectra is also in agreement with this model. The results for Co2+ in quartz are diVerent from Co-bearing spinel and staurolite and other silicates like orthopyroxene, olivine, and beryls. The formation process of the color center is discussed.pt_BR
dc.language.isoen_USpt_BR
dc.rightsrestritopt_BR
dc.subjectSynthetic quartzpt_BR
dc.subjectElectron paramagnetic resonancept_BR
dc.subjectOptical absorptionpt_BR
dc.titleOrigin of the color in cobalt-doped quartz.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.identifier.uri2https://link.springer.com/article/10.1007/s00269-011-0434-3pt_BR
dc.identifier.doihttps://doi.org/10.1007/s00269-011-0434-3-
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