Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates

Detalhes bibliográficos
Autor(a) principal: Siqueira,Kisla P. F.
Data de Publicação: 2014
Outros Autores: Dias,Anderson
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Materials research (São Carlos. Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000700027
Resumo: The influence of the synthesis parameters on the crystalline structures of orthotantalate ceramics has been investigated. Powder materials were prepared by the solid-state reaction route. X-ray diffraction and Raman scattering measurements were employed to investigate the crystal structure of the produced materials. In this work, we analyzed three different examples in which the temperature and time were decisive on the final crystal structure of LnTaO4 compounds besides the lanthanide ionic size. Firstly, the thermal evolution for NdTaO4 samples showed that mixed crystal phases are formed up to 1100 ºC, while well-crystallized M-NdTaO4 (I2/a) materials are obtained in temperatures higher than 1200 ºC. Also, the influence of the synthesis time was investigated for the LaTaO4 ceramics: it was necessary 14 h to obtain samples in the P2(1)/c structure. Finally, two polymorphs could be obtained for the DyTaO4 ceramics: P2/a and I2/a space groups were obtained at 1300 ºC and 1500 ºC, respectively. This study indicated that the temperature, time and lanthanide size are directly correlated with the crystalline arrangement of the orthotantalate materials.
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spelling Effect of the processing parameters on the crystalline structure of lanthanide orthotantalatessolid-state processinglanthanide orthotantalatescrystal structureRaman spectroscopyThe influence of the synthesis parameters on the crystalline structures of orthotantalate ceramics has been investigated. Powder materials were prepared by the solid-state reaction route. X-ray diffraction and Raman scattering measurements were employed to investigate the crystal structure of the produced materials. In this work, we analyzed three different examples in which the temperature and time were decisive on the final crystal structure of LnTaO4 compounds besides the lanthanide ionic size. Firstly, the thermal evolution for NdTaO4 samples showed that mixed crystal phases are formed up to 1100 ºC, while well-crystallized M-NdTaO4 (I2/a) materials are obtained in temperatures higher than 1200 ºC. Also, the influence of the synthesis time was investigated for the LaTaO4 ceramics: it was necessary 14 h to obtain samples in the P2(1)/c structure. Finally, two polymorphs could be obtained for the DyTaO4 ceramics: P2/a and I2/a space groups were obtained at 1300 ºC and 1500 ºC, respectively. This study indicated that the temperature, time and lanthanide size are directly correlated with the crystalline arrangement of the orthotantalate materials.ABM, ABC, ABPol2014-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000700027Materials Research v.17 suppl.1 2014reponame:Materials research (São Carlos. Online)instname:Universidade Federal de São Carlos (UFSCAR)instacron:ABM ABC ABPOL10.1590/S1516-14392013005000189info:eu-repo/semantics/openAccessSiqueira,Kisla P. F.Dias,Andersoneng2015-11-06T00:00:00Zoai:scielo:S1516-14392014000700027Revistahttp://www.scielo.br/mrPUBhttps://old.scielo.br/oai/scielo-oai.phpdedz@power.ufscar.br1980-53731516-1439opendoar:2015-11-06T00:00Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)false
dc.title.none.fl_str_mv Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
title Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
spellingShingle Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
Siqueira,Kisla P. F.
solid-state processing
lanthanide orthotantalates
crystal structure
Raman spectroscopy
title_short Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
title_full Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
title_fullStr Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
title_full_unstemmed Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
title_sort Effect of the processing parameters on the crystalline structure of lanthanide orthotantalates
author Siqueira,Kisla P. F.
author_facet Siqueira,Kisla P. F.
Dias,Anderson
author_role author
author2 Dias,Anderson
author2_role author
dc.contributor.author.fl_str_mv Siqueira,Kisla P. F.
Dias,Anderson
dc.subject.por.fl_str_mv solid-state processing
lanthanide orthotantalates
crystal structure
Raman spectroscopy
topic solid-state processing
lanthanide orthotantalates
crystal structure
Raman spectroscopy
description The influence of the synthesis parameters on the crystalline structures of orthotantalate ceramics has been investigated. Powder materials were prepared by the solid-state reaction route. X-ray diffraction and Raman scattering measurements were employed to investigate the crystal structure of the produced materials. In this work, we analyzed three different examples in which the temperature and time were decisive on the final crystal structure of LnTaO4 compounds besides the lanthanide ionic size. Firstly, the thermal evolution for NdTaO4 samples showed that mixed crystal phases are formed up to 1100 ºC, while well-crystallized M-NdTaO4 (I2/a) materials are obtained in temperatures higher than 1200 ºC. Also, the influence of the synthesis time was investigated for the LaTaO4 ceramics: it was necessary 14 h to obtain samples in the P2(1)/c structure. Finally, two polymorphs could be obtained for the DyTaO4 ceramics: P2/a and I2/a space groups were obtained at 1300 ºC and 1500 ºC, respectively. This study indicated that the temperature, time and lanthanide size are directly correlated with the crystalline arrangement of the orthotantalate materials.
publishDate 2014
dc.date.none.fl_str_mv 2014-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000700027
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000700027
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1516-14392013005000189
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv ABM, ABC, ABPol
publisher.none.fl_str_mv ABM, ABC, ABPol
dc.source.none.fl_str_mv Materials Research v.17 suppl.1 2014
reponame:Materials research (São Carlos. Online)
instname:Universidade Federal de São Carlos (UFSCAR)
instacron:ABM ABC ABPOL
instname_str Universidade Federal de São Carlos (UFSCAR)
instacron_str ABM ABC ABPOL
institution ABM ABC ABPOL
reponame_str Materials research (São Carlos. Online)
collection Materials research (São Carlos. Online)
repository.name.fl_str_mv Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)
repository.mail.fl_str_mv dedz@power.ufscar.br
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