Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers

Detalhes bibliográficos
Autor(a) principal: Spitzer,Marcos
Data de Publicação: 2000
Outros Autores: Silva,Luís H.M. da, Loh,Watson
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000400009
Resumo: Phase equilibrium data were determined for ternary systems containing ethylene oxide oligomers or polymers, heptane and one of three organic solvents (methanol, dichloromethane or chloroform). The effects of temperature, of polymer molecular weight and of the chemical nature of the organic solvent on phase equilibrium were investigated. For all the studied systems, the miscibility region was reduced as temperature decreased, indicating an exothermic phase separation process. For both binary and ternary mixtures, the miscibility also decreased as the macromolecule size increased, although this effect was less significant for the ternary mixtures. These features suggest that phase separation is more influenced by enthalpic than entropic contributions. Regarding the different polar solvents investigated, methanol presented a much smaller miscibility region, in accordance with its inferior solvation ability for PEO. The largest miscibility region was observed with chloroform, not much different from the behaviour observed with dichloromethane. Tie lines were determined for some systems, confirming the strong segregation between polymer and the hydrocarbon solvent.
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spelling Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymerspoly(ethylene oxide)liquid-liquid equilibriapolymer solutionspreferential solvationPhase equilibrium data were determined for ternary systems containing ethylene oxide oligomers or polymers, heptane and one of three organic solvents (methanol, dichloromethane or chloroform). The effects of temperature, of polymer molecular weight and of the chemical nature of the organic solvent on phase equilibrium were investigated. For all the studied systems, the miscibility region was reduced as temperature decreased, indicating an exothermic phase separation process. For both binary and ternary mixtures, the miscibility also decreased as the macromolecule size increased, although this effect was less significant for the ternary mixtures. These features suggest that phase separation is more influenced by enthalpic than entropic contributions. Regarding the different polar solvents investigated, methanol presented a much smaller miscibility region, in accordance with its inferior solvation ability for PEO. The largest miscibility region was observed with chloroform, not much different from the behaviour observed with dichloromethane. Tie lines were determined for some systems, confirming the strong segregation between polymer and the hydrocarbon solvent.Sociedade Brasileira de Química2000-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000400009Journal of the Brazilian Chemical Society v.11 n.4 2000reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532000000400009info:eu-repo/semantics/openAccessSpitzer,MarcosSilva,Luís H.M. daLoh,Watsoneng2000-11-17T00:00:00Zoai:scielo:S0103-50532000000400009Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2000-11-17T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
title Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
spellingShingle Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
Spitzer,Marcos
poly(ethylene oxide)
liquid-liquid equilibria
polymer solutions
preferential solvation
title_short Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
title_full Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
title_fullStr Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
title_full_unstemmed Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
title_sort Liquid biphase systems formed in ternary mixtures of two organic solvents and ethylene oxide oligomers or polymers
author Spitzer,Marcos
author_facet Spitzer,Marcos
Silva,Luís H.M. da
Loh,Watson
author_role author
author2 Silva,Luís H.M. da
Loh,Watson
author2_role author
author
dc.contributor.author.fl_str_mv Spitzer,Marcos
Silva,Luís H.M. da
Loh,Watson
dc.subject.por.fl_str_mv poly(ethylene oxide)
liquid-liquid equilibria
polymer solutions
preferential solvation
topic poly(ethylene oxide)
liquid-liquid equilibria
polymer solutions
preferential solvation
description Phase equilibrium data were determined for ternary systems containing ethylene oxide oligomers or polymers, heptane and one of three organic solvents (methanol, dichloromethane or chloroform). The effects of temperature, of polymer molecular weight and of the chemical nature of the organic solvent on phase equilibrium were investigated. For all the studied systems, the miscibility region was reduced as temperature decreased, indicating an exothermic phase separation process. For both binary and ternary mixtures, the miscibility also decreased as the macromolecule size increased, although this effect was less significant for the ternary mixtures. These features suggest that phase separation is more influenced by enthalpic than entropic contributions. Regarding the different polar solvents investigated, methanol presented a much smaller miscibility region, in accordance with its inferior solvation ability for PEO. The largest miscibility region was observed with chloroform, not much different from the behaviour observed with dichloromethane. Tie lines were determined for some systems, confirming the strong segregation between polymer and the hydrocarbon solvent.
publishDate 2000
dc.date.none.fl_str_mv 2000-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000400009
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000400009
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532000000400009
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.11 n.4 2000
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
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instname_str Sociedade Brasileira de Química (SBQ)
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institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
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