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dc.contributor.authorSENOL, A
dc.contributor.authorSAYAR, AA
dc.date.accessioned2021-03-05T13:30:15Z
dc.date.available2021-03-05T13:30:15Z
dc.identifier.citationSENOL A., SAYAR A., "LIQUID-LIQUID EQUILIBRIA OF SOME WATER PLUS TETRAHYDROFURFURYL ALCOHOL PLUS SOLVENT TERNARIES AT 293.2+/-0.1 K AND 101.3+/-0.8 KPA", FLUID PHASE EQUILIBRIA, cilt.106, ss.169-183, 1995
dc.identifier.issn0378-3812
dc.identifier.othervv_1032021
dc.identifier.otherav_b28b656d-6ffc-4184-8501-f2dcbc4cc83d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/118937
dc.identifier.urihttps://doi.org/10.1016/0378-3812(94)02621-7
dc.description.abstractIsothermal solubility curves and tie-line end compositions for five water + tetrahydrofurfuryl alcohol + solvent ternaries were experimentally determined at 293.2 +/- 0.1 K and 101.3 +/- 0.8 kPa. Cyclohexanone, 2-methylbutyl ethanoate, 1,2-dichloroethane, 1-octanol and ethyl acetate were used as solvents. Tie-lines were predicted using the LLE-data UNIFAC model. Somewhat acceptable results were obtained for the 1,2-dichloroethane and I-octanol ternaries, whereas the model failed to generate reliable results for the remaining ternaries. Comparison of the extracting capabilities of the investigated solvents were made with respect to distribution coefficients, separation factors and solvent-free selectivity bases.1,2-Dichloroethane and I-octanol exhibited the best solvent performance in the separation of tetrahydrofurfuryl alcohol, especially from its dilute aqueous solutions.
dc.language.isoeng
dc.subjectKimya Mühendisliği ve Teknolojisi
dc.subjectFizikokimya
dc.subjectTemel Bilimler
dc.subjectMühendislik ve Teknoloji
dc.subjectTemel Bilimler (SCI)
dc.subjectMÜHENDİSLİK, KİMYASAL
dc.subjectKimya
dc.subjectKİMYA, FİZİKSEL
dc.subjectMühendislik, Bilişim ve Teknoloji (ENG)
dc.subjectMühendislik
dc.subjectTERMODİNAMİK
dc.titleLIQUID-LIQUID EQUILIBRIA OF SOME WATER PLUS TETRAHYDROFURFURYL ALCOHOL PLUS SOLVENT TERNARIES AT 293.2+/-0.1 K AND 101.3+/-0.8 KPA
dc.typeMakale
dc.relation.journalFLUID PHASE EQUILIBRIA
dc.contributor.department, ,
dc.identifier.volume106
dc.identifier.startpage169
dc.identifier.endpage183
dc.contributor.firstauthorID116155


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