NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles

Detalhes bibliográficos
Autor(a) principal: Norek, Małgorzata
Data de Publicação: 2007
Outros Autores: Pereira, Giovannia A., Geraldes, Carlos F. G. C., Denkova, Antonia, Zhou, Wuzong, Peters, Joop A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10389
https://doi.org/10.1021/jp072288l
Resumo: Aqueous suspensions of paramagnetic lanthanide oxide nanoparticles have been studied by NMR relaxometry. The observed relaxivities are explained by the static dephasing regime (SDR) theory. The corresponding R2 relaxivities are considerably smaller and are strongly dependent on the interval between the two refocusing pulses. The experimental data are rationalized by assuming the value of the diffusion correlation time, τD, to be very long in a layer with adsorbed xanthan on the particle's surface. In this layer, the refocusing pulses are fully effective and R2 ≈ 0. Outside this layer, the diffusion model for weakly magnetized particles was applied. From the fit of the experimental relaxation data with this model, both the particle radii (rp) and the radii of the spheres, within which the refocusing pulses are fully effective (rdiff), were estimated. The values of rp obtained are in agreement with those determined by dynamic light scattering. Because the value of rdiff depends on the external magnetic field B and on the magnetic moment of the lanthanide of interest (μeff2), the R2 relaxivity was found to be proportional to B and to μeff2.
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spelling NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide NanoparticlesAqueous suspensions of paramagnetic lanthanide oxide nanoparticles have been studied by NMR relaxometry. The observed relaxivities are explained by the static dephasing regime (SDR) theory. The corresponding R2 relaxivities are considerably smaller and are strongly dependent on the interval between the two refocusing pulses. The experimental data are rationalized by assuming the value of the diffusion correlation time, τD, to be very long in a layer with adsorbed xanthan on the particle's surface. In this layer, the refocusing pulses are fully effective and R2 ≈ 0. Outside this layer, the diffusion model for weakly magnetized particles was applied. From the fit of the experimental relaxation data with this model, both the particle radii (rp) and the radii of the spheres, within which the refocusing pulses are fully effective (rdiff), were estimated. The values of rp obtained are in agreement with those determined by dynamic light scattering. Because the value of rdiff depends on the external magnetic field B and on the magnetic moment of the lanthanide of interest (μeff2), the R2 relaxivity was found to be proportional to B and to μeff2.American Chemical Society2007-07-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10389http://hdl.handle.net/10316/10389https://doi.org/10.1021/jp072288lengThe Journal of Physical Chemistry C. 111:28 (2007) 10240-102461932-7447Norek, MałgorzataPereira, Giovannia A.Geraldes, Carlos F. G. C.Denkova, AntoniaZhou, WuzongPeters, Joop A.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:RCAAP2021-10-12T09:17:12Zoai:estudogeral.uc.pt:10316/10389Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:46.299479Repositório 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 NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
title NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
spellingShingle NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
Norek, Małgorzata
title_short NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
title_full NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
title_fullStr NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
title_full_unstemmed NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
title_sort NMR Transversal Relaxivity of Suspensions of Lanthanide Oxide Nanoparticles
author Norek, Małgorzata
author_facet Norek, Małgorzata
Pereira, Giovannia A.
Geraldes, Carlos F. G. C.
Denkova, Antonia
Zhou, Wuzong
Peters, Joop A.
author_role author
author2 Pereira, Giovannia A.
Geraldes, Carlos F. G. C.
Denkova, Antonia
Zhou, Wuzong
Peters, Joop A.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Norek, Małgorzata
Pereira, Giovannia A.
Geraldes, Carlos F. G. C.
Denkova, Antonia
Zhou, Wuzong
Peters, Joop A.
description Aqueous suspensions of paramagnetic lanthanide oxide nanoparticles have been studied by NMR relaxometry. The observed relaxivities are explained by the static dephasing regime (SDR) theory. The corresponding R2 relaxivities are considerably smaller and are strongly dependent on the interval between the two refocusing pulses. The experimental data are rationalized by assuming the value of the diffusion correlation time, τD, to be very long in a layer with adsorbed xanthan on the particle's surface. In this layer, the refocusing pulses are fully effective and R2 ≈ 0. Outside this layer, the diffusion model for weakly magnetized particles was applied. From the fit of the experimental relaxation data with this model, both the particle radii (rp) and the radii of the spheres, within which the refocusing pulses are fully effective (rdiff), were estimated. The values of rp obtained are in agreement with those determined by dynamic light scattering. Because the value of rdiff depends on the external magnetic field B and on the magnetic moment of the lanthanide of interest (μeff2), the R2 relaxivity was found to be proportional to B and to μeff2.
publishDate 2007
dc.date.none.fl_str_mv 2007-07-19
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/10316/10389
http://hdl.handle.net/10316/10389
https://doi.org/10.1021/jp072288l
url http://hdl.handle.net/10316/10389
https://doi.org/10.1021/jp072288l
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv The Journal of Physical Chemistry C. 111:28 (2007) 10240-10246
1932-7447
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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