Time domain NMR evaluation of poly(vinyl alcohol) xerogels
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Polímeros (São Carlos. Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-14282016000300221 |
Resumo: | Abstract Poly(vinyl alcohol) (PVA)-based chemically cross-linked xerogels, both neat and loaded with nanoparticulate hydrophilic silica (SiO2), were obtained and characterized mainly through time domain NMR experiments (TD-NMR). Fourier-transform infrared (FT-IR) and wide angle X-ray diffraction (WAXD) analyses were employed as secondary methods. TD-NMR, through the interpretation of the spin-lattice relaxation constant values and related information, showed both cross-linking and nanoparticle influences on PVA matrix. SiO2 does not interact chemically with the PVA chains, but has effect on its molecular mobility, as investigated via TD-NMR. Apparent energy of activation, spin-lattice time constant and size of spin domains in the sample have almost linear dependence with the degree of cross-linking of the PVA and are affected by the addition of SiO2. These three parameters were derived from a single set of TD-NMR experiments, which demonstrates the versatility of the technique for characterization of inorganic-organic hybrid xerogels, an important class of materials. |
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Time domain NMR evaluation of poly(vinyl alcohol) xerogelsinorganic-organic hybridpolymer gelsrelaxometrylow-field nuclear magnetic resonancetime domain nuclear magnetic resonanceAbstract Poly(vinyl alcohol) (PVA)-based chemically cross-linked xerogels, both neat and loaded with nanoparticulate hydrophilic silica (SiO2), were obtained and characterized mainly through time domain NMR experiments (TD-NMR). Fourier-transform infrared (FT-IR) and wide angle X-ray diffraction (WAXD) analyses were employed as secondary methods. TD-NMR, through the interpretation of the spin-lattice relaxation constant values and related information, showed both cross-linking and nanoparticle influences on PVA matrix. SiO2 does not interact chemically with the PVA chains, but has effect on its molecular mobility, as investigated via TD-NMR. Apparent energy of activation, spin-lattice time constant and size of spin domains in the sample have almost linear dependence with the degree of cross-linking of the PVA and are affected by the addition of SiO2. These three parameters were derived from a single set of TD-NMR experiments, which demonstrates the versatility of the technique for characterization of inorganic-organic hybrid xerogels, an important class of materials.Associação Brasileira de Polímeros2016-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-14282016000300221Polímeros v.26 n.3 2016reponame:Polímeros (São Carlos. Online)instname:Associação Brasileira de Polímeros (ABPol)instacron:ABPO10.1590/0104-1428.2093info:eu-repo/semantics/openAccessRodrigues,Elton Jorge da RochaCavalcante,Maxwell de PaulaTavares,Maria Inês Brunoeng2016-12-20T00:00:00Zoai:scielo:S0104-14282016000300221Revistahttp://www.scielo.br/pohttps://old.scielo.br/oai/scielo-oai.php||revista@abpol.org.br1678-51690104-1428opendoar:2016-12-20T00:00Polímeros (São Carlos. Online) - Associação Brasileira de Polímeros (ABPol)false |
dc.title.none.fl_str_mv |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels |
title |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels |
spellingShingle |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels Rodrigues,Elton Jorge da Rocha inorganic-organic hybrid polymer gels relaxometry low-field nuclear magnetic resonance time domain nuclear magnetic resonance |
title_short |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels |
title_full |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels |
title_fullStr |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels |
title_full_unstemmed |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels |
title_sort |
Time domain NMR evaluation of poly(vinyl alcohol) xerogels |
author |
Rodrigues,Elton Jorge da Rocha |
author_facet |
Rodrigues,Elton Jorge da Rocha Cavalcante,Maxwell de Paula Tavares,Maria Inês Bruno |
author_role |
author |
author2 |
Cavalcante,Maxwell de Paula Tavares,Maria Inês Bruno |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Rodrigues,Elton Jorge da Rocha Cavalcante,Maxwell de Paula Tavares,Maria Inês Bruno |
dc.subject.por.fl_str_mv |
inorganic-organic hybrid polymer gels relaxometry low-field nuclear magnetic resonance time domain nuclear magnetic resonance |
topic |
inorganic-organic hybrid polymer gels relaxometry low-field nuclear magnetic resonance time domain nuclear magnetic resonance |
description |
Abstract Poly(vinyl alcohol) (PVA)-based chemically cross-linked xerogels, both neat and loaded with nanoparticulate hydrophilic silica (SiO2), were obtained and characterized mainly through time domain NMR experiments (TD-NMR). Fourier-transform infrared (FT-IR) and wide angle X-ray diffraction (WAXD) analyses were employed as secondary methods. TD-NMR, through the interpretation of the spin-lattice relaxation constant values and related information, showed both cross-linking and nanoparticle influences on PVA matrix. SiO2 does not interact chemically with the PVA chains, but has effect on its molecular mobility, as investigated via TD-NMR. Apparent energy of activation, spin-lattice time constant and size of spin domains in the sample have almost linear dependence with the degree of cross-linking of the PVA and are affected by the addition of SiO2. These three parameters were derived from a single set of TD-NMR experiments, which demonstrates the versatility of the technique for characterization of inorganic-organic hybrid xerogels, an important class of materials. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-09-01 |
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=S0104-14282016000300221 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-14282016000300221 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0104-1428.2093 |
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 |
Associação Brasileira de Polímeros |
publisher.none.fl_str_mv |
Associação Brasileira de Polímeros |
dc.source.none.fl_str_mv |
Polímeros v.26 n.3 2016 reponame:Polímeros (São Carlos. Online) instname:Associação Brasileira de Polímeros (ABPol) instacron:ABPO |
instname_str |
Associação Brasileira de Polímeros (ABPol) |
instacron_str |
ABPO |
institution |
ABPO |
reponame_str |
Polímeros (São Carlos. Online) |
collection |
Polímeros (São Carlos. Online) |
repository.name.fl_str_mv |
Polímeros (São Carlos. Online) - Associação Brasileira de Polímeros (ABPol) |
repository.mail.fl_str_mv |
||revista@abpol.org.br |
_version_ |
1754212589630390272 |