Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer

Detalhes bibliográficos
Autor(a) principal: Tapia, María José
Data de Publicação: 2002
Outros Autores: Burrows, Hugh D.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10445
https://doi.org/10.1021/la015613j
Resumo: The interaction between trivalent lanthanide ions and the polyelectrolyte poly(vinyl sulfonate) (PVS) has been studied in aqueous solutions by monitoring lanthanide luminescence. The existence of specific binding of cations by PVS is indicated by blue-shifts in the maximum of the emission of cerium(III), effects on the decay of terbium(III) luminescence, and a slight broadening of the gadolinium(III) electron paramagnetic resonance (EPR). From the isotope effect observed on the decay of luminescence of Tb(III) bound to PVS in H2O and D2O solutions, it is suggested that complexation leads to a decrease in the number of bound water molecules from nine to three. In mixed PVS systems containing Ce(III) and Tb(III), energy transfer is observed. The efficiency of this is found to fit a multiple equilibrium model. The slope of the corresponding plot is shown to provide an effective measure of the extent of lanthanide binding to the polyelectrolyte. This is found to increase with temperature but to decrease upon addition of alcohols. The effect of alcohols is found to depend on their chain length, suggesting the importance of hydrophobic interactions. Increasing ionic strength by adding NaCl increases ion binding, while complex behavior, due to competing effects and precipitation, is observed upon addition of tetraalkylammonium bromide surfactants. Finally, from the energy-transfer data, it is possible to estimate the distance between lanthanide ions on the polyelectrolyte chain. Lanthanide luminescence promises to be an excellent technique for studying the interaction between metal ions and polyelectrolytes in aqueous solutions.
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spelling Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy TransferThe interaction between trivalent lanthanide ions and the polyelectrolyte poly(vinyl sulfonate) (PVS) has been studied in aqueous solutions by monitoring lanthanide luminescence. The existence of specific binding of cations by PVS is indicated by blue-shifts in the maximum of the emission of cerium(III), effects on the decay of terbium(III) luminescence, and a slight broadening of the gadolinium(III) electron paramagnetic resonance (EPR). From the isotope effect observed on the decay of luminescence of Tb(III) bound to PVS in H2O and D2O solutions, it is suggested that complexation leads to a decrease in the number of bound water molecules from nine to three. In mixed PVS systems containing Ce(III) and Tb(III), energy transfer is observed. The efficiency of this is found to fit a multiple equilibrium model. The slope of the corresponding plot is shown to provide an effective measure of the extent of lanthanide binding to the polyelectrolyte. This is found to increase with temperature but to decrease upon addition of alcohols. The effect of alcohols is found to depend on their chain length, suggesting the importance of hydrophobic interactions. Increasing ionic strength by adding NaCl increases ion binding, while complex behavior, due to competing effects and precipitation, is observed upon addition of tetraalkylammonium bromide surfactants. Finally, from the energy-transfer data, it is possible to estimate the distance between lanthanide ions on the polyelectrolyte chain. Lanthanide luminescence promises to be an excellent technique for studying the interaction between metal ions and polyelectrolytes in aqueous solutions.American Chemical Society2002-03-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10445http://hdl.handle.net/10316/10445https://doi.org/10.1021/la015613jengLangmuir. 18:5 (2002) 1872-18760743-7463Tapia, María JoséBurrows, Hugh D.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-11-03T10:09:12Zoai:estudogeral.uc.pt:10316/10445Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:30.790220Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
title Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
spellingShingle Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
Tapia, María José
title_short Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
title_full Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
title_fullStr Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
title_full_unstemmed Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
title_sort Cation Polyelectrolyte Interactions in Aqueous Sodium Poly(vinyl sulfonate) as Seen by Ce3+ to Tb3+ Energy Transfer
author Tapia, María José
author_facet Tapia, María José
Burrows, Hugh D.
author_role author
author2 Burrows, Hugh D.
author2_role author
dc.contributor.author.fl_str_mv Tapia, María José
Burrows, Hugh D.
description The interaction between trivalent lanthanide ions and the polyelectrolyte poly(vinyl sulfonate) (PVS) has been studied in aqueous solutions by monitoring lanthanide luminescence. The existence of specific binding of cations by PVS is indicated by blue-shifts in the maximum of the emission of cerium(III), effects on the decay of terbium(III) luminescence, and a slight broadening of the gadolinium(III) electron paramagnetic resonance (EPR). From the isotope effect observed on the decay of luminescence of Tb(III) bound to PVS in H2O and D2O solutions, it is suggested that complexation leads to a decrease in the number of bound water molecules from nine to three. In mixed PVS systems containing Ce(III) and Tb(III), energy transfer is observed. The efficiency of this is found to fit a multiple equilibrium model. The slope of the corresponding plot is shown to provide an effective measure of the extent of lanthanide binding to the polyelectrolyte. This is found to increase with temperature but to decrease upon addition of alcohols. The effect of alcohols is found to depend on their chain length, suggesting the importance of hydrophobic interactions. Increasing ionic strength by adding NaCl increases ion binding, while complex behavior, due to competing effects and precipitation, is observed upon addition of tetraalkylammonium bromide surfactants. Finally, from the energy-transfer data, it is possible to estimate the distance between lanthanide ions on the polyelectrolyte chain. Lanthanide luminescence promises to be an excellent technique for studying the interaction between metal ions and polyelectrolytes in aqueous solutions.
publishDate 2002
dc.date.none.fl_str_mv 2002-03-05
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10445
http://hdl.handle.net/10316/10445
https://doi.org/10.1021/la015613j
url http://hdl.handle.net/10316/10445
https://doi.org/10.1021/la015613j
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Langmuir. 18:5 (2002) 1872-1876
0743-7463
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dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
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