Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography

Autores
Castells, Reynaldo César; Castells, Cecilia Beatriz Marta
Año de publicación
1992
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The activity coefficients of fifteen hydrocarbons at infinite dilution in tetra-n-octyltin were measured using gas-liquid chromatography at five temperatures between 40 and 60°C. Partial molar excess thermodynamic properties are calculated from the experimental results, and discussed within the framework of the equation of state theory of Flory and of the Ising fluid theory of Sanchez and Lacombe. Both theories results in binary mixture characteristic parameters (X12 and ΔP*, respectively) that decrease linearly with the temperature. The results may be interpreted by assuming that there is orientational order in pure tetra-n-octyltin and in pure n-alkanes, but not in the remaining solutes; the destruction of this order on mixing the hydrocarbons with the tin compound results in important contributions to the excess thermodynamic properties.
Centro de Investigación y Desarrollo en Tecnología de Pinturas
Facultad de Ciencias Exactas
Materia
Química
Tetra-n-octyltin
hydrocarbon solutions
activity coefficients
gas chromatography
Flory theory
Sanchez-Lacombe theory
excess enthalpy
orientational order
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/143653

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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatographyCastells, Reynaldo CésarCastells, Cecilia Beatriz MartaQuímicaTetra-n-octyltinhydrocarbon solutionsactivity coefficientsgas chromatographyFlory theorySanchez-Lacombe theoryexcess enthalpyorientational orderThe activity coefficients of fifteen hydrocarbons at infinite dilution in tetra-n-octyltin were measured using gas-liquid chromatography at five temperatures between 40 and 60°C. Partial molar excess thermodynamic properties are calculated from the experimental results, and discussed within the framework of the equation of state theory of Flory and of the Ising fluid theory of Sanchez and Lacombe. Both theories results in binary mixture characteristic parameters (X12 and ΔP*, respectively) that decrease linearly with the temperature. The results may be interpreted by assuming that there is orientational order in pure tetra-n-octyltin and in pure n-alkanes, but not in the remaining solutes; the destruction of this order on mixing the hydrocarbons with the tin compound results in important contributions to the excess thermodynamic properties.Centro de Investigación y Desarrollo en Tecnología de PinturasFacultad de Ciencias Exactas1992info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf129-146http://sedici.unlp.edu.ar/handle/10915/143653enginfo:eu-repo/semantics/altIdentifier/issn/0095-9782info:eu-repo/semantics/altIdentifier/issn/1572-8927info:eu-repo/semantics/altIdentifier/doi/10.1007/bf00647003info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:32:01Zoai:sedici.unlp.edu.ar:10915/143653Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:32:02.203SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
title Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
spellingShingle Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
Castells, Reynaldo César
Química
Tetra-n-octyltin
hydrocarbon solutions
activity coefficients
gas chromatography
Flory theory
Sanchez-Lacombe theory
excess enthalpy
orientational order
title_short Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
title_full Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
title_fullStr Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
title_full_unstemmed Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
title_sort Thermodynamics of Tetra-n-octyltin+ hydrocarbon systems by gas-liquid chromatography
dc.creator.none.fl_str_mv Castells, Reynaldo César
Castells, Cecilia Beatriz Marta
author Castells, Reynaldo César
author_facet Castells, Reynaldo César
Castells, Cecilia Beatriz Marta
author_role author
author2 Castells, Cecilia Beatriz Marta
author2_role author
dc.subject.none.fl_str_mv Química
Tetra-n-octyltin
hydrocarbon solutions
activity coefficients
gas chromatography
Flory theory
Sanchez-Lacombe theory
excess enthalpy
orientational order
topic Química
Tetra-n-octyltin
hydrocarbon solutions
activity coefficients
gas chromatography
Flory theory
Sanchez-Lacombe theory
excess enthalpy
orientational order
dc.description.none.fl_txt_mv The activity coefficients of fifteen hydrocarbons at infinite dilution in tetra-n-octyltin were measured using gas-liquid chromatography at five temperatures between 40 and 60°C. Partial molar excess thermodynamic properties are calculated from the experimental results, and discussed within the framework of the equation of state theory of Flory and of the Ising fluid theory of Sanchez and Lacombe. Both theories results in binary mixture characteristic parameters (X12 and ΔP*, respectively) that decrease linearly with the temperature. The results may be interpreted by assuming that there is orientational order in pure tetra-n-octyltin and in pure n-alkanes, but not in the remaining solutes; the destruction of this order on mixing the hydrocarbons with the tin compound results in important contributions to the excess thermodynamic properties.
Centro de Investigación y Desarrollo en Tecnología de Pinturas
Facultad de Ciencias Exactas
description The activity coefficients of fifteen hydrocarbons at infinite dilution in tetra-n-octyltin were measured using gas-liquid chromatography at five temperatures between 40 and 60°C. Partial molar excess thermodynamic properties are calculated from the experimental results, and discussed within the framework of the equation of state theory of Flory and of the Ising fluid theory of Sanchez and Lacombe. Both theories results in binary mixture characteristic parameters (X12 and ΔP*, respectively) that decrease linearly with the temperature. The results may be interpreted by assuming that there is orientational order in pure tetra-n-octyltin and in pure n-alkanes, but not in the remaining solutes; the destruction of this order on mixing the hydrocarbons with the tin compound results in important contributions to the excess thermodynamic properties.
publishDate 1992
dc.date.none.fl_str_mv 1992
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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://sedici.unlp.edu.ar/handle/10915/143653
url http://sedici.unlp.edu.ar/handle/10915/143653
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0095-9782
info:eu-repo/semantics/altIdentifier/issn/1572-8927
info:eu-repo/semantics/altIdentifier/doi/10.1007/bf00647003
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
129-146
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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