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Solubilities of cinnamic acid esters in ionic liquids

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dc.contributor.author Panteli, EK en
dc.contributor.author Voutsas, EK en
dc.date.accessioned 2014-03-01T01:31:56Z
dc.date.available 2014-03-01T01:31:56Z
dc.date.issued 2009 en
dc.identifier.issn 0021-9568 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/19985
dc.subject.classification Chemistry, Multidisciplinary en
dc.subject.classification Engineering, Chemical en
dc.subject.other Alkyl chain lengths en
dc.subject.other Cinnamic acids en
dc.subject.other Experimental datum en
dc.subject.other Ferulate en
dc.subject.other Gibbs energies en
dc.subject.other Imidazolium cations en
dc.subject.other Imidazolium-based ionic liquids en
dc.subject.other Nrtl activity coefficient models en
dc.subject.other Positive values en
dc.subject.other Thermodynamic functions en
dc.subject.other Uniquac en
dc.subject.other Van't hoff equations en
dc.subject.other Acids en
dc.subject.other Alkylation en
dc.subject.other Esterification en
dc.subject.other Esters en
dc.subject.other Ionization of liquids en
dc.subject.other Negative ions en
dc.subject.other Positive ions en
dc.subject.other Solubility en
dc.subject.other Ionic liquids en
dc.title Solubilities of cinnamic acid esters in ionic liquids en
heal.type journalArticle en
heal.identifier.primary 10.1021/je800596c en
heal.identifier.secondary http://dx.doi.org/10.1021/je800596c en
heal.language English en
heal.publicationDate 2009 en
heal.abstract The solubilities of three cinnamic acid esters, namely, methyl ferulate, methyl p-coumarate, and methyl sinapate, in eight imidazolium-based ionic liquids composed of the PF6- and BF4- anions have been measured at (30, 39, and 48) °C. Higher solubilities of the three esters were observed in the ionic liquids composed of the BF4- anion than those composed of the PF6- anion. Also, higher solubilities are observed in alkyl-substituted (on the imidazolium cation moiety) ILs than in polar-substituted ILs, whereas, as the alkyl chain length on the cation moiety increases, the solubility increases as well. Moreover, using the van't Hoff equations, the apparent Gibbs energy, enthalpy, and entropy of solution were calculated. Positive values of the three thermodynamic functions were found in all cases. Finally, successful correlations of the experimental data were achieved with the UNIQUAC and the NRTL activity coefficient models. © 2009 American Chemical Society. en
heal.publisher AMER CHEMICAL SOC en
heal.journalName Journal of Chemical and Engineering Data en
dc.identifier.doi 10.1021/je800596c en
dc.identifier.isi ISI:000264197700023 en
dc.identifier.volume 54 en
dc.identifier.issue 3 en
dc.identifier.spage 812 en
dc.identifier.epage 818 en


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