Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes

Autores
Martínez Casillas, Diana Cristina; Longinotti, María Paula; Bruno, Mariano Martín; Vaca Chávez Fornasero, Fabián; Acosta, Rodolfo Héctor; Corti, Horacio Roberto
Año de publicación
2018
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The diffusion of alkaline chlorides (LiCl, KCl, and CsCl) and water in mesoporous silica samples with pore sizes covering the range from micropores (2 nm) up to mesopores larger than 30 nm have been measured by resorting to a simple diffusional technique in the case of electrolytes and 1H NMR in the case of water. The morphology of the silica samples varies from a microporous structure, an interconnected network of pores, and typical mesoporous materials with ink-bottle pores, with increasing pore size. The release of electrolytes from the silica as a function of time exhibits two differentiated regimes, at short and long times, which correlates quite well with the size of the pores and that of necks of the pores, respectively. The diffusion of water inside the pores follows the same trend with pore size that the diffusion of electrolytes, indicating a coupling between the ions and water diffusional mobilities. The tortuosity effect on the diffusion of all studied electrolytes and water shows a monotonic slight increase with decreasing diameter for pores larger than 5 nm, while the tortuosity factor increases markedly for smaller pores. In microporous and mesoporous silica with pore sizes below 10 nm, the tortuosity factor of Li+ ion is much larger than those for K+ and Cs+ ions, since its diffusion is hindered by a stronger electrostatic interaction with the ionizable silanol groups on the pore wall; and also larger than that for water diffusion which it is retarded by a weaker hydrogen bond interaction with the silanol groups. The differences in tortuosity factors among alkaline chlorides and water become negligible for pore sizes larger than 10 nm. The spin-lattice relaxation time measurements of 1H-water and Li+ ions confirm this behavior.
Fil: Martínez Casillas, Diana Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Longinotti, María Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Bruno, Mariano Martín. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina
Fil: Vaca Chávez Fornasero, Fabián. Universidad Nacional de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Acosta, Rodolfo Héctor. Universidad Nacional de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Corti, Horacio Roberto. Comisión Nacional de Energía Atómica. Gerencia del Área Investigaciones y Aplicaciones no Nucleares; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Materia
Silica
Difusion
Litio
Agua
Litio
Nivel de accesibilidad
acceso abierto
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
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CONICET Digital (CONICET)
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Consejo Nacional de Investigaciones Científicas y Técnicas
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oai:ri.conicet.gov.ar:11336/89511
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spelling Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore SizesMartínez Casillas, Diana CristinaLonginotti, María PaulaBruno, Mariano MartínVaca Chávez Fornasero, FabiánAcosta, Rodolfo HéctorCorti, Horacio RobertoSilicaDifusionLitioAguaLitiohttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The diffusion of alkaline chlorides (LiCl, KCl, and CsCl) and water in mesoporous silica samples with pore sizes covering the range from micropores (2 nm) up to mesopores larger than 30 nm have been measured by resorting to a simple diffusional technique in the case of electrolytes and 1H NMR in the case of water. The morphology of the silica samples varies from a microporous structure, an interconnected network of pores, and typical mesoporous materials with ink-bottle pores, with increasing pore size. The release of electrolytes from the silica as a function of time exhibits two differentiated regimes, at short and long times, which correlates quite well with the size of the pores and that of necks of the pores, respectively. The diffusion of water inside the pores follows the same trend with pore size that the diffusion of electrolytes, indicating a coupling between the ions and water diffusional mobilities. The tortuosity effect on the diffusion of all studied electrolytes and water shows a monotonic slight increase with decreasing diameter for pores larger than 5 nm, while the tortuosity factor increases markedly for smaller pores. In microporous and mesoporous silica with pore sizes below 10 nm, the tortuosity factor of Li+ ion is much larger than those for K+ and Cs+ ions, since its diffusion is hindered by a stronger electrostatic interaction with the ionizable silanol groups on the pore wall; and also larger than that for water diffusion which it is retarded by a weaker hydrogen bond interaction with the silanol groups. The differences in tortuosity factors among alkaline chlorides and water become negligible for pore sizes larger than 10 nm. The spin-lattice relaxation time measurements of 1H-water and Li+ ions confirm this behavior.Fil: Martínez Casillas, Diana Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Longinotti, María Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Bruno, Mariano Martín. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: Vaca Chávez Fornasero, Fabián. Universidad Nacional de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Acosta, Rodolfo Héctor. Universidad Nacional de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Corti, Horacio Roberto. Comisión Nacional de Energía Atómica. Gerencia del Área Investigaciones y Aplicaciones no Nucleares; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaAmerican Chemical Society2018-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/89511Martínez Casillas, Diana Cristina; Longinotti, María Paula; Bruno, Mariano Martín; Vaca Chávez Fornasero, Fabián; Acosta, Rodolfo Héctor; et al.; Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes; American Chemical Society; Journal of Physical Chemistry C; 122; 6; 2-2018; 3638-36471932-74471932-7455CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/acs.jpcc.7b11555info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpcc.7b11555info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-12T09:33:41Zoai:ri.conicet.gov.ar:11336/89511instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-11-12 09:33:41.659CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
title Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
spellingShingle Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
Martínez Casillas, Diana Cristina
Silica
Difusion
Litio
Agua
Litio
title_short Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
title_full Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
title_fullStr Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
title_full_unstemmed Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
title_sort Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes
dc.creator.none.fl_str_mv Martínez Casillas, Diana Cristina
Longinotti, María Paula
Bruno, Mariano Martín
Vaca Chávez Fornasero, Fabián
Acosta, Rodolfo Héctor
Corti, Horacio Roberto
author Martínez Casillas, Diana Cristina
author_facet Martínez Casillas, Diana Cristina
Longinotti, María Paula
Bruno, Mariano Martín
Vaca Chávez Fornasero, Fabián
Acosta, Rodolfo Héctor
Corti, Horacio Roberto
author_role author
author2 Longinotti, María Paula
Bruno, Mariano Martín
Vaca Chávez Fornasero, Fabián
Acosta, Rodolfo Héctor
Corti, Horacio Roberto
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Silica
Difusion
Litio
Agua
Litio
topic Silica
Difusion
Litio
Agua
Litio
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The diffusion of alkaline chlorides (LiCl, KCl, and CsCl) and water in mesoporous silica samples with pore sizes covering the range from micropores (2 nm) up to mesopores larger than 30 nm have been measured by resorting to a simple diffusional technique in the case of electrolytes and 1H NMR in the case of water. The morphology of the silica samples varies from a microporous structure, an interconnected network of pores, and typical mesoporous materials with ink-bottle pores, with increasing pore size. The release of electrolytes from the silica as a function of time exhibits two differentiated regimes, at short and long times, which correlates quite well with the size of the pores and that of necks of the pores, respectively. The diffusion of water inside the pores follows the same trend with pore size that the diffusion of electrolytes, indicating a coupling between the ions and water diffusional mobilities. The tortuosity effect on the diffusion of all studied electrolytes and water shows a monotonic slight increase with decreasing diameter for pores larger than 5 nm, while the tortuosity factor increases markedly for smaller pores. In microporous and mesoporous silica with pore sizes below 10 nm, the tortuosity factor of Li+ ion is much larger than those for K+ and Cs+ ions, since its diffusion is hindered by a stronger electrostatic interaction with the ionizable silanol groups on the pore wall; and also larger than that for water diffusion which it is retarded by a weaker hydrogen bond interaction with the silanol groups. The differences in tortuosity factors among alkaline chlorides and water become negligible for pore sizes larger than 10 nm. The spin-lattice relaxation time measurements of 1H-water and Li+ ions confirm this behavior.
Fil: Martínez Casillas, Diana Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Longinotti, María Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Bruno, Mariano Martín. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina
Fil: Vaca Chávez Fornasero, Fabián. Universidad Nacional de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Acosta, Rodolfo Héctor. Universidad Nacional de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Corti, Horacio Roberto. Comisión Nacional de Energía Atómica. Gerencia del Área Investigaciones y Aplicaciones no Nucleares; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
description The diffusion of alkaline chlorides (LiCl, KCl, and CsCl) and water in mesoporous silica samples with pore sizes covering the range from micropores (2 nm) up to mesopores larger than 30 nm have been measured by resorting to a simple diffusional technique in the case of electrolytes and 1H NMR in the case of water. The morphology of the silica samples varies from a microporous structure, an interconnected network of pores, and typical mesoporous materials with ink-bottle pores, with increasing pore size. The release of electrolytes from the silica as a function of time exhibits two differentiated regimes, at short and long times, which correlates quite well with the size of the pores and that of necks of the pores, respectively. The diffusion of water inside the pores follows the same trend with pore size that the diffusion of electrolytes, indicating a coupling between the ions and water diffusional mobilities. The tortuosity effect on the diffusion of all studied electrolytes and water shows a monotonic slight increase with decreasing diameter for pores larger than 5 nm, while the tortuosity factor increases markedly for smaller pores. In microporous and mesoporous silica with pore sizes below 10 nm, the tortuosity factor of Li+ ion is much larger than those for K+ and Cs+ ions, since its diffusion is hindered by a stronger electrostatic interaction with the ionizable silanol groups on the pore wall; and also larger than that for water diffusion which it is retarded by a weaker hydrogen bond interaction with the silanol groups. The differences in tortuosity factors among alkaline chlorides and water become negligible for pore sizes larger than 10 nm. The spin-lattice relaxation time measurements of 1H-water and Li+ ions confirm this behavior.
publishDate 2018
dc.date.none.fl_str_mv 2018-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/89511
Martínez Casillas, Diana Cristina; Longinotti, María Paula; Bruno, Mariano Martín; Vaca Chávez Fornasero, Fabián; Acosta, Rodolfo Héctor; et al.; Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes; American Chemical Society; Journal of Physical Chemistry C; 122; 6; 2-2018; 3638-3647
1932-7447
1932-7455
CONICET Digital
CONICET
url http://hdl.handle.net/11336/89511
identifier_str_mv Martínez Casillas, Diana Cristina; Longinotti, María Paula; Bruno, Mariano Martín; Vaca Chávez Fornasero, Fabián; Acosta, Rodolfo Héctor; et al.; Diffusion of Water and Electrolytes in Mesoporous Silica with a Wide Range of Pore Sizes; American Chemical Society; Journal of Physical Chemistry C; 122; 6; 2-2018; 3638-3647
1932-7447
1932-7455
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/acs.jpcc.7b11555
info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpcc.7b11555
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
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dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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