Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K

Detalhes bibliográficos
Autor(a) principal: Veloso, Anne C. G.
Data de Publicação: 2018
Outros Autores: Patrício, amela R., Quintão, Juan C., Carvalho, Raquel M. M. de, Silva, Luis H. M. da, Hespanhol, Maria C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: LOCUS Repositório Institucional da UFV
Texto Completo: https://doi.org/10.1016/j.fluid.2018.04.017
http://www.locus.ufv.br/handle/123456789/21771
Resumo: Liquid-liquid equilibrium data of aqueous two-phase systems (ATPS) composed by L35 triblock copolymer + ammonium electrolytes (nitrate, NO3−; tartrate, C4H4O62−; phosphate, HPO42−; acetate, C2H3O2−) + water, at different temperatures (298.2 and 313.2 K) are presented in this paper. The experimental ATPS data were correlated with the original and modified non-random two-liquid (NRTL) for predicting energetic parameters of the studied systems. The results were satisfactory with global root mean square deviations (33 tie-lines) of the 2.36% and 2.53% for the original and modified models, respectively. The effect of the temperature and electrolyte nature on the biphasic area position was investigated. The increase of the temperature promoted a slight increase in the two-phase region indicating the endothermic character of the phase splitting. The increase in the temperature also promoted a rise in the module of the slope of the tie-lines. The anions ability to promote phase separation followed the order: HPO42− > C4H4O62− > NO3− > C2H3O2−.
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spelling Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 KAqueous two-phase systemsLiquid-liquid equilibriumAmmonium saltsL35NRTLLiquid-liquid equilibrium data of aqueous two-phase systems (ATPS) composed by L35 triblock copolymer + ammonium electrolytes (nitrate, NO3−; tartrate, C4H4O62−; phosphate, HPO42−; acetate, C2H3O2−) + water, at different temperatures (298.2 and 313.2 K) are presented in this paper. The experimental ATPS data were correlated with the original and modified non-random two-liquid (NRTL) for predicting energetic parameters of the studied systems. The results were satisfactory with global root mean square deviations (33 tie-lines) of the 2.36% and 2.53% for the original and modified models, respectively. The effect of the temperature and electrolyte nature on the biphasic area position was investigated. The increase of the temperature promoted a slight increase in the two-phase region indicating the endothermic character of the phase splitting. The increase in the temperature also promoted a rise in the module of the slope of the tie-lines. The anions ability to promote phase separation followed the order: HPO42− > C4H4O62− > NO3− > C2H3O2−.Fluid Phase Equilibria2018-09-11T19:38:56Z2018-09-11T19:38:56Z2018-08-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlepdfapplication/pdf03783812https://doi.org/10.1016/j.fluid.2018.04.017http://www.locus.ufv.br/handle/123456789/21771engv. 469, p. 26- 32, ago. 2018Elsevier B.V.info:eu-repo/semantics/openAccessVeloso, Anne C. G.Patrício, amela R.Quintão, Juan C.Carvalho, Raquel M. M. deSilva, Luis H. M. daHespanhol, Maria C.reponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFV2024-07-12T08:10:00Zoai:locus.ufv.br:123456789/21771Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452024-07-12T08:10LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.none.fl_str_mv Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
title Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
spellingShingle Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
Veloso, Anne C. G.
Aqueous two-phase systems
Liquid-liquid equilibrium
Ammonium salts
L35
NRTL
title_short Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
title_full Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
title_fullStr Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
title_full_unstemmed Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
title_sort Phase equilibrium of aqueous two-phase systems composed by L35 triblock copolymer + organic and inorganic ammonium electrolytes + water at 298.2 and 313.2 K
author Veloso, Anne C. G.
author_facet Veloso, Anne C. G.
Patrício, amela R.
Quintão, Juan C.
Carvalho, Raquel M. M. de
Silva, Luis H. M. da
Hespanhol, Maria C.
author_role author
author2 Patrício, amela R.
Quintão, Juan C.
Carvalho, Raquel M. M. de
Silva, Luis H. M. da
Hespanhol, Maria C.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Veloso, Anne C. G.
Patrício, amela R.
Quintão, Juan C.
Carvalho, Raquel M. M. de
Silva, Luis H. M. da
Hespanhol, Maria C.
dc.subject.por.fl_str_mv Aqueous two-phase systems
Liquid-liquid equilibrium
Ammonium salts
L35
NRTL
topic Aqueous two-phase systems
Liquid-liquid equilibrium
Ammonium salts
L35
NRTL
description Liquid-liquid equilibrium data of aqueous two-phase systems (ATPS) composed by L35 triblock copolymer + ammonium electrolytes (nitrate, NO3−; tartrate, C4H4O62−; phosphate, HPO42−; acetate, C2H3O2−) + water, at different temperatures (298.2 and 313.2 K) are presented in this paper. The experimental ATPS data were correlated with the original and modified non-random two-liquid (NRTL) for predicting energetic parameters of the studied systems. The results were satisfactory with global root mean square deviations (33 tie-lines) of the 2.36% and 2.53% for the original and modified models, respectively. The effect of the temperature and electrolyte nature on the biphasic area position was investigated. The increase of the temperature promoted a slight increase in the two-phase region indicating the endothermic character of the phase splitting. The increase in the temperature also promoted a rise in the module of the slope of the tie-lines. The anions ability to promote phase separation followed the order: HPO42− > C4H4O62− > NO3− > C2H3O2−.
publishDate 2018
dc.date.none.fl_str_mv 2018-09-11T19:38:56Z
2018-09-11T19:38:56Z
2018-08-15
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 03783812
https://doi.org/10.1016/j.fluid.2018.04.017
http://www.locus.ufv.br/handle/123456789/21771
identifier_str_mv 03783812
url https://doi.org/10.1016/j.fluid.2018.04.017
http://www.locus.ufv.br/handle/123456789/21771
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv v. 469, p. 26- 32, ago. 2018
dc.rights.driver.fl_str_mv Elsevier B.V.
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Elsevier B.V.
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv pdf
application/pdf
dc.publisher.none.fl_str_mv Fluid Phase Equilibria
publisher.none.fl_str_mv Fluid Phase Equilibria
dc.source.none.fl_str_mv reponame:LOCUS Repositório Institucional da UFV
instname:Universidade Federal de Viçosa (UFV)
instacron:UFV
instname_str Universidade Federal de Viçosa (UFV)
instacron_str UFV
institution UFV
reponame_str LOCUS Repositório Institucional da UFV
collection LOCUS Repositório Institucional da UFV
repository.name.fl_str_mv LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)
repository.mail.fl_str_mv fabiojreis@ufv.br
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