Isoconversional kinetics of vaporization of nanoconfined liquids

Detalhes bibliográficos
Autor(a) principal: Ekawa, Bruno [UNESP]
Data de Publicação: 2021
Outros Autores: Stanford, Victoria L., Vyazovkin, Sergey
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.molliq.2020.114824
http://hdl.handle.net/11449/209312
Resumo: Isoconversional kinetic analysis is applied to thermogravimetry data on vaporization of n-decane and dimethyl sulfoxide from alumina nanopores and bulk. For bulk vaporization, the isoconversional activation energy is independent of conversion and equal to the enthalpy of vaporization. For vaporization from nanopores, the isoconversional activation energy varies stronglywith conversion, passing through aminimumat midrange conversions. This behavior is shown to be consistent with the successive transition of the rate control fromthe Kelvin effect to Knudsen diffusion, and eventually to surface diffusion. All three phenomena are demonstrated to have their specific activation energies. It has been determined that the deceleration of vaporization from nanopores is due to a dramatic decrease in the value of the preexponential factor. The decrease is linked to the high frequency of collisions with the pore walls and to a possibility of adsorption on the walls. (C) 2020 Elsevier B.V. All rights reserved.
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spelling Isoconversional kinetics of vaporization of nanoconfined liquidsArrhenius equationEvaporationKinetic parametersMass lossNanoRate constantThermogravimetry (TGA)Isoconversional kinetic analysis is applied to thermogravimetry data on vaporization of n-decane and dimethyl sulfoxide from alumina nanopores and bulk. For bulk vaporization, the isoconversional activation energy is independent of conversion and equal to the enthalpy of vaporization. For vaporization from nanopores, the isoconversional activation energy varies stronglywith conversion, passing through aminimumat midrange conversions. This behavior is shown to be consistent with the successive transition of the rate control fromthe Kelvin effect to Knudsen diffusion, and eventually to surface diffusion. All three phenomena are demonstrated to have their specific activation energies. It has been determined that the deceleration of vaporization from nanopores is due to a dramatic decrease in the value of the preexponential factor. The decrease is linked to the high frequency of collisions with the pore walls and to a possibility of adsorption on the walls. (C) 2020 Elsevier B.V. All rights reserved.Univ Alabama Birmingham, Dept Chem, 901 S 14th St, Birmingham, AL 35294 USAUniv Estadual Paulista, Inst Quim, CP 355, BR-14801970 Araraquara, SP, BrazilUniv Estadual Paulista, Inst Quim, CP 355, BR-14801970 Araraquara, SP, BrazilElsevier B.V.Univ Alabama BirminghamUniversidade Estadual Paulista (Unesp)Ekawa, Bruno [UNESP]Stanford, Victoria L.Vyazovkin, Sergey2021-06-25T11:55:57Z2021-06-25T11:55:57Z2021-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article7http://dx.doi.org/10.1016/j.molliq.2020.114824Journal Of Molecular Liquids. Amsterdam: Elsevier, v. 327, 7 p., 2021.0167-7322http://hdl.handle.net/11449/20931210.1016/j.molliq.2020.114824WOS:000637200400027Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Molecular Liquidsinfo:eu-repo/semantics/openAccess2021-10-23T19:28:03Zoai:repositorio.unesp.br:11449/209312Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T19:28:03Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Isoconversional kinetics of vaporization of nanoconfined liquids
title Isoconversional kinetics of vaporization of nanoconfined liquids
spellingShingle Isoconversional kinetics of vaporization of nanoconfined liquids
Ekawa, Bruno [UNESP]
Arrhenius equation
Evaporation
Kinetic parameters
Mass loss
Nano
Rate constant
Thermogravimetry (TGA)
title_short Isoconversional kinetics of vaporization of nanoconfined liquids
title_full Isoconversional kinetics of vaporization of nanoconfined liquids
title_fullStr Isoconversional kinetics of vaporization of nanoconfined liquids
title_full_unstemmed Isoconversional kinetics of vaporization of nanoconfined liquids
title_sort Isoconversional kinetics of vaporization of nanoconfined liquids
author Ekawa, Bruno [UNESP]
author_facet Ekawa, Bruno [UNESP]
Stanford, Victoria L.
Vyazovkin, Sergey
author_role author
author2 Stanford, Victoria L.
Vyazovkin, Sergey
author2_role author
author
dc.contributor.none.fl_str_mv Univ Alabama Birmingham
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Ekawa, Bruno [UNESP]
Stanford, Victoria L.
Vyazovkin, Sergey
dc.subject.por.fl_str_mv Arrhenius equation
Evaporation
Kinetic parameters
Mass loss
Nano
Rate constant
Thermogravimetry (TGA)
topic Arrhenius equation
Evaporation
Kinetic parameters
Mass loss
Nano
Rate constant
Thermogravimetry (TGA)
description Isoconversional kinetic analysis is applied to thermogravimetry data on vaporization of n-decane and dimethyl sulfoxide from alumina nanopores and bulk. For bulk vaporization, the isoconversional activation energy is independent of conversion and equal to the enthalpy of vaporization. For vaporization from nanopores, the isoconversional activation energy varies stronglywith conversion, passing through aminimumat midrange conversions. This behavior is shown to be consistent with the successive transition of the rate control fromthe Kelvin effect to Knudsen diffusion, and eventually to surface diffusion. All three phenomena are demonstrated to have their specific activation energies. It has been determined that the deceleration of vaporization from nanopores is due to a dramatic decrease in the value of the preexponential factor. The decrease is linked to the high frequency of collisions with the pore walls and to a possibility of adsorption on the walls. (C) 2020 Elsevier B.V. All rights reserved.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T11:55:57Z
2021-06-25T11:55:57Z
2021-04-01
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://dx.doi.org/10.1016/j.molliq.2020.114824
Journal Of Molecular Liquids. Amsterdam: Elsevier, v. 327, 7 p., 2021.
0167-7322
http://hdl.handle.net/11449/209312
10.1016/j.molliq.2020.114824
WOS:000637200400027
url http://dx.doi.org/10.1016/j.molliq.2020.114824
http://hdl.handle.net/11449/209312
identifier_str_mv Journal Of Molecular Liquids. Amsterdam: Elsevier, v. 327, 7 p., 2021.
0167-7322
10.1016/j.molliq.2020.114824
WOS:000637200400027
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Molecular Liquids
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 7
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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