Collective diffusion in charge-stabilized suspensions: Concentration and salt effects

Autores
Gapinski, J.; Patkowski, A.; Banchio, Adolfo Javier; Holmqvist, P.; Meier, Guillermo Enrique; Lettinga, M.P.; Nägele, G.
Año de publicación
2007
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The authors present a joint experimental-theoretical study of collective diffusion properties in aqueous suspensions of charge-stabilized fluorinated latex spheres. Small-angle x-ray scattering and x-ray photon correlation spectroscopy have been used to explore the concentration and ionic-strength dependence of the static and short-time dynamic properties including the hydrodynamic function H (q), the wave-number-dependent collective diffusion coefficient D (q), and the intermediate scattering function over the entire accessible range. They show that all experimental data can be quantitatively described and explained by means of a recently developed accelerated Stokesian dynamics simulation method, in combination with a modified hydrodynamic many-body theory. In particular, the behavior of H (q) for de-ionized and dense suspensions can be attributed to the influence of many-body hydrodynamics, without any need for postulating hydrodynamic screening to be present, as it was done in earlier work. Upper and lower boundaries are provided for the peak height of the hydrodynamic function and for the short-time self-diffusion coefficient over the entire range of added salt concentrations.
Fil: Gapinski, J.. A. Mickiewicz University; Polonia
Fil: Patkowski, A.. A. Mickiewicz University; Polonia
Fil: Banchio, Adolfo Javier. 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: Holmqvist, P.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
Fil: Meier, Guillermo Enrique. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
Fil: Lettinga, M.P.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
Fil: Nägele, G.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
Materia
Charge-stabilized suspension
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/132357

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network_name_str CONICET Digital (CONICET)
spelling Collective diffusion in charge-stabilized suspensions: Concentration and salt effectsGapinski, J.Patkowski, A.Banchio, Adolfo JavierHolmqvist, P.Meier, Guillermo EnriqueLettinga, M.P.Nägele, G.Charge-stabilized suspensionhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1The authors present a joint experimental-theoretical study of collective diffusion properties in aqueous suspensions of charge-stabilized fluorinated latex spheres. Small-angle x-ray scattering and x-ray photon correlation spectroscopy have been used to explore the concentration and ionic-strength dependence of the static and short-time dynamic properties including the hydrodynamic function H (q), the wave-number-dependent collective diffusion coefficient D (q), and the intermediate scattering function over the entire accessible range. They show that all experimental data can be quantitatively described and explained by means of a recently developed accelerated Stokesian dynamics simulation method, in combination with a modified hydrodynamic many-body theory. In particular, the behavior of H (q) for de-ionized and dense suspensions can be attributed to the influence of many-body hydrodynamics, without any need for postulating hydrodynamic screening to be present, as it was done in earlier work. Upper and lower boundaries are provided for the peak height of the hydrodynamic function and for the short-time self-diffusion coefficient over the entire range of added salt concentrations.Fil: Gapinski, J.. A. Mickiewicz University; PoloniaFil: Patkowski, A.. A. Mickiewicz University; PoloniaFil: Banchio, Adolfo Javier. 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: Holmqvist, P.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; AlemaniaFil: Meier, Guillermo Enrique. Helmholtz Gemeinschaft. Forschungszentrum Jülich; AlemaniaFil: Lettinga, M.P.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; AlemaniaFil: Nägele, G.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; AlemaniaAmerican Institute of Physics2007-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/132357Gapinski, J.; Patkowski, A.; Banchio, Adolfo Javier; Holmqvist, P.; Meier, Guillermo Enrique; et al.; Collective diffusion in charge-stabilized suspensions: Concentration and salt effects; American Institute of Physics; Journal of Chemical Physics; 126; 10; 12-2007; 1-120021-96061089-7690CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1063/1.2538891info:eu-repo/semantics/altIdentifier/url/https://aip.scitation.org/doi/10.1063/1.2538891info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:48:57Zoai:ri.conicet.gov.ar:11336/132357instacron: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:34982025-09-29 09:48:57.916CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
title Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
spellingShingle Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
Gapinski, J.
Charge-stabilized suspension
title_short Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
title_full Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
title_fullStr Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
title_full_unstemmed Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
title_sort Collective diffusion in charge-stabilized suspensions: Concentration and salt effects
dc.creator.none.fl_str_mv Gapinski, J.
Patkowski, A.
Banchio, Adolfo Javier
Holmqvist, P.
Meier, Guillermo Enrique
Lettinga, M.P.
Nägele, G.
author Gapinski, J.
author_facet Gapinski, J.
Patkowski, A.
Banchio, Adolfo Javier
Holmqvist, P.
Meier, Guillermo Enrique
Lettinga, M.P.
Nägele, G.
author_role author
author2 Patkowski, A.
Banchio, Adolfo Javier
Holmqvist, P.
Meier, Guillermo Enrique
Lettinga, M.P.
Nägele, G.
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Charge-stabilized suspension
topic Charge-stabilized suspension
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.3
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The authors present a joint experimental-theoretical study of collective diffusion properties in aqueous suspensions of charge-stabilized fluorinated latex spheres. Small-angle x-ray scattering and x-ray photon correlation spectroscopy have been used to explore the concentration and ionic-strength dependence of the static and short-time dynamic properties including the hydrodynamic function H (q), the wave-number-dependent collective diffusion coefficient D (q), and the intermediate scattering function over the entire accessible range. They show that all experimental data can be quantitatively described and explained by means of a recently developed accelerated Stokesian dynamics simulation method, in combination with a modified hydrodynamic many-body theory. In particular, the behavior of H (q) for de-ionized and dense suspensions can be attributed to the influence of many-body hydrodynamics, without any need for postulating hydrodynamic screening to be present, as it was done in earlier work. Upper and lower boundaries are provided for the peak height of the hydrodynamic function and for the short-time self-diffusion coefficient over the entire range of added salt concentrations.
Fil: Gapinski, J.. A. Mickiewicz University; Polonia
Fil: Patkowski, A.. A. Mickiewicz University; Polonia
Fil: Banchio, Adolfo Javier. 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: Holmqvist, P.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
Fil: Meier, Guillermo Enrique. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
Fil: Lettinga, M.P.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
Fil: Nägele, G.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania
description The authors present a joint experimental-theoretical study of collective diffusion properties in aqueous suspensions of charge-stabilized fluorinated latex spheres. Small-angle x-ray scattering and x-ray photon correlation spectroscopy have been used to explore the concentration and ionic-strength dependence of the static and short-time dynamic properties including the hydrodynamic function H (q), the wave-number-dependent collective diffusion coefficient D (q), and the intermediate scattering function over the entire accessible range. They show that all experimental data can be quantitatively described and explained by means of a recently developed accelerated Stokesian dynamics simulation method, in combination with a modified hydrodynamic many-body theory. In particular, the behavior of H (q) for de-ionized and dense suspensions can be attributed to the influence of many-body hydrodynamics, without any need for postulating hydrodynamic screening to be present, as it was done in earlier work. Upper and lower boundaries are provided for the peak height of the hydrodynamic function and for the short-time self-diffusion coefficient over the entire range of added salt concentrations.
publishDate 2007
dc.date.none.fl_str_mv 2007-12
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/11336/132357
Gapinski, J.; Patkowski, A.; Banchio, Adolfo Javier; Holmqvist, P.; Meier, Guillermo Enrique; et al.; Collective diffusion in charge-stabilized suspensions: Concentration and salt effects; American Institute of Physics; Journal of Chemical Physics; 126; 10; 12-2007; 1-12
0021-9606
1089-7690
CONICET Digital
CONICET
url http://hdl.handle.net/11336/132357
identifier_str_mv Gapinski, J.; Patkowski, A.; Banchio, Adolfo Javier; Holmqvist, P.; Meier, Guillermo Enrique; et al.; Collective diffusion in charge-stabilized suspensions: Concentration and salt effects; American Institute of Physics; Journal of Chemical Physics; 126; 10; 12-2007; 1-12
0021-9606
1089-7690
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1063/1.2538891
info:eu-repo/semantics/altIdentifier/url/https://aip.scitation.org/doi/10.1063/1.2538891
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
dc.publisher.none.fl_str_mv American Institute of Physics
publisher.none.fl_str_mv American Institute of Physics
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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