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dc.contributor.authorBabaei, M
dc.contributor.authorShayanfar, A
dc.contributor.authorRahimpour, E
dc.contributor.authorBarzegar-Jalali, M
dc.contributor.authorMartinez, F
dc.contributor.authorJouyban, A
dc.date.accessioned2018-08-26T09:35:27Z
dc.date.available2018-08-26T09:35:27Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57874
dc.description.abstractSolubility measurements were performed for bosentan (BST) in binary mixtures of propylene glycol (PG) and water at atmospheric pressure within the temperature range, T = 293.2 - 313.2 K by employing a shake-flask method. Generated solubility data were correlated with Jouyban-Acree-van't Hoff model and the accuracies of the predicted solubilities and model performance were illustrated by mean relative deviations (MRD). Furthermore, the apparent thermodynamic properties of BST dissolving in all the mixed solvents were calculated, and the obtained results show that the dissolution process is endothermic. By using the inverse Kirkwood-Buff integrals, it was observed that BST is preferentially solvated by water in water-rich solvent mixtures and preferentially solvated by PG (as a cosolvent) in the composition range of 0.20 < x1 < 1.00 at 298.2 K. © 2018 Informa UK Limited, trading as Taylor & Francis Group
dc.language.isoEnglish
dc.relation.ispartofPhysics and Chemistry of Liquids
dc.subjectAtmospheric pressure
dc.subjectGlycols
dc.subjectPolyols
dc.subjectPropylene
dc.subjectSolubility
dc.subjectSolvents
dc.subjectThermodynamic properties
dc.subjectBinary solvent mixtures
dc.subjectBosentan
dc.subjectDissolution process
dc.subjectPreferential solvation
dc.subjectPropylene glycols
dc.subjectRelative deviations
dc.subjectShake-flask method
dc.subjectSolubility measurement
dc.subjectBinary mixtures
dc.titleSolubility of bosentan in {propylene glycol + water} mixtures at various temperatures: experimental data and mathematical modelling
dc.typeArticle
dc.citation.spage1
dc.citation.epage11
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1080/00319104.2018.1461872


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