Chemical modification of niobium layered oxide by tetraalkylammonium intercalation
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000700024 |
Resumo: | Chemical modification of the layered K4Nb6O17 material was systematically investigated through the reaction of its proton-exchanged form (H2K2Nb6O17) in alkaline solutions containing tetramethylammonium (tma+), tetraethylammonium (tea+) or tetrapropylammonium (tpa+) cations. The intercalated amount reaches 50% (for tma+), 25% (for tea+) and 15% (for tpa+) of the H2K2Nb6O17 negative charge (concerning the exchange at interlayer I) due to the steric hindrance of larger cations. Hexaniobate samples present (020) basal reflections equal to 23.0, 26.3 and 26.5 Å once intercalated respectively with tma+, tea+ and tpa+. When samples are heated above 200-250 ºC, CO2 evolution is observed; Hofmann elimination reaction is also detected for hexaniobate-tpa+ samples. Scanning electron microscopy images show the predominance of plate-like particles; stick-like particles are also observed for samples containing bulky ions. The intercalation reaction is promoted in the order tma+ > tea+ > tpa+, while the formation of a dispersion of colloidal particles is facilitated in the inverse order. |
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Chemical modification of niobium layered oxide by tetraalkylammonium intercalationlayered niobatehexaniobatetetraalkylammoniumintercalationChemical modification of the layered K4Nb6O17 material was systematically investigated through the reaction of its proton-exchanged form (H2K2Nb6O17) in alkaline solutions containing tetramethylammonium (tma+), tetraethylammonium (tea+) or tetrapropylammonium (tpa+) cations. The intercalated amount reaches 50% (for tma+), 25% (for tea+) and 15% (for tpa+) of the H2K2Nb6O17 negative charge (concerning the exchange at interlayer I) due to the steric hindrance of larger cations. Hexaniobate samples present (020) basal reflections equal to 23.0, 26.3 and 26.5 Å once intercalated respectively with tma+, tea+ and tpa+. When samples are heated above 200-250 ºC, CO2 evolution is observed; Hofmann elimination reaction is also detected for hexaniobate-tpa+ samples. Scanning electron microscopy images show the predominance of plate-like particles; stick-like particles are also observed for samples containing bulky ions. The intercalation reaction is promoted in the order tma+ > tea+ > tpa+, while the formation of a dispersion of colloidal particles is facilitated in the inverse order.Sociedade Brasileira de Química2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000700024Journal of the Brazilian Chemical Society v.21 n.7 2010reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532010000700024info:eu-repo/semantics/openAccessShiguihara,Ana L.Bizeto,Marcos A.Constantino,Vera R. L.eng2010-07-30T00:00:00Zoai:scielo:S0103-50532010000700024Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-07-30T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation |
title |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation |
spellingShingle |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation Shiguihara,Ana L. layered niobate hexaniobate tetraalkylammonium intercalation |
title_short |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation |
title_full |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation |
title_fullStr |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation |
title_full_unstemmed |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation |
title_sort |
Chemical modification of niobium layered oxide by tetraalkylammonium intercalation |
author |
Shiguihara,Ana L. |
author_facet |
Shiguihara,Ana L. Bizeto,Marcos A. Constantino,Vera R. L. |
author_role |
author |
author2 |
Bizeto,Marcos A. Constantino,Vera R. L. |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Shiguihara,Ana L. Bizeto,Marcos A. Constantino,Vera R. L. |
dc.subject.por.fl_str_mv |
layered niobate hexaniobate tetraalkylammonium intercalation |
topic |
layered niobate hexaniobate tetraalkylammonium intercalation |
description |
Chemical modification of the layered K4Nb6O17 material was systematically investigated through the reaction of its proton-exchanged form (H2K2Nb6O17) in alkaline solutions containing tetramethylammonium (tma+), tetraethylammonium (tea+) or tetrapropylammonium (tpa+) cations. The intercalated amount reaches 50% (for tma+), 25% (for tea+) and 15% (for tpa+) of the H2K2Nb6O17 negative charge (concerning the exchange at interlayer I) due to the steric hindrance of larger cations. Hexaniobate samples present (020) basal reflections equal to 23.0, 26.3 and 26.5 Å once intercalated respectively with tma+, tea+ and tpa+. When samples are heated above 200-250 ºC, CO2 evolution is observed; Hofmann elimination reaction is also detected for hexaniobate-tpa+ samples. Scanning electron microscopy images show the predominance of plate-like particles; stick-like particles are also observed for samples containing bulky ions. The intercalation reaction is promoted in the order tma+ > tea+ > tpa+, while the formation of a dispersion of colloidal particles is facilitated in the inverse order. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-01-01 |
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=S0103-50532010000700024 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000700024 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532010000700024 |
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 |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.21 n.7 2010 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
_version_ |
1750318171095564288 |