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Study of liquid–liquid equilibria at different temperatures of water + ethanol + 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide tern…

2016

Abstract The experimental liquid–liquid equilibria (LLE) data of the water + ethanol + 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([bmp][Tf2N]) system has been measured at different temperatures in this work. The LLE of the system has been measured at between 283 and 333 K. The UNIQUAC and NRTL models were used to correlate the LLE data and good results were obtained in both cases, however UNIQUAC gave a more accurate correlation. In order to apply the UNIQUAC model the volume and surface parameters for [bmp][Tf2N] (r, q) were determined. Finally, in order to obtain ethanol from the aqueous mixture, the solvent capability of the ionic liquid was checked and compared wit…

UNIQUACAqueous solutionEthanolTernary numeral system010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryGeneral Physics and Astronomy02 engineering and technology01 natural sciences0104 chemical sciencesSolventchemistry.chemical_compound020401 chemical engineeringchemistryIonic liquidNon-random two-liquid modelPhysical chemistry0204 chemical engineeringPhysical and Theoretical ChemistryImideFluid Phase Equilibria
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Separation of the azeotropic mixture 2-propanol + water employing different imidazolium ionic liquids as solvents

2020

Abstract The liquid-liquid equilibria of the ternary systems water (1) + 2-propanol (2) + [emim][Tf2N] (3) and water (1) + 2-propanol (2) + [hmim][Tf2N] (3) at 283.2, 303.2 and 323.2 K and atmospheric pressure were investigated, in order to achieve a better knowledge of the ternary mixture behaviour. The capability of [emim][Tf2N] and [hmim][Tf2N] as solvents in the separation of the azeotropic mixture water + 2-propanol was studied through the distribution coefficient and selectivity, and compared with the results obtained with other ionic liquids in the same azeotropic mixture studied before by our research group. The thermodynamic parameters of both ternary mixtures were calculated by th…

UNIQUACAtmospheric pressureChemistry02 engineering and technology010402 general chemistry01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesPropanolPartition coefficientchemistry.chemical_compound020401 chemical engineeringIonic liquidNon-random two-liquid modelPhysical chemistryGeneral Materials Science0204 chemical engineeringPhysical and Theoretical ChemistrySelectivityTernary operationThe Journal of Chemical Thermodynamics
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Phase equilibria and variation of the azeotropic composition with pressure for binary mixtures of 1-propanol + chlorobenzene and 1-butanol + chlorobe…

1998

Abstract Isobaric vapor-liquid equilibria were obtained for the systems 1-propanol + chlorobenzene and 1-butanol + chlorobenzene at 200 and 300 kPa using a dynamic still. The mole fraction of the alcohol in the azeotropic point increases with pressure and for the 1-propanol + chlorobenzene system at 300 kPa, the azeotrope has disappeared. The two systems satisfy the point-to-point thermodynamic consistency test. Both systems show a positive deviation from ideality. The data were well correlated with the Margules, van Laar, Wilson. NRTL and UNIQUAC equations.

UNIQUACChemistryGeneral Chemical EngineeringButanolGeneral Physics and AstronomyThermodynamicsMole fractionchemistry.chemical_compound1-PropanolChlorobenzeneAzeotropeNon-random two-liquid modelIsobaric processPhysical and Theoretical ChemistryFluid Phase Equilibria
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Vapor–liquid equilibrium of binary mixtures of chlorobenzene with 3-methyl-1-butanol, 3-methyl-2-butanol and 2-methyl-2-butanol, at 100 kPa

1998

Abstract Isobaric vapor–liquid equilibria have been obtained for the systems 3-methyl-1-butanol+chlorobenzene, 3-methyl-2-butanol+chlorobenzene and 2-methyl-2-butanol+chlorobenzene at 100 kPa, using a dynamic still. The experimental error in temperature is ±0.1 K, in pressure ±0.1 kPa, and in the liquid and vapor mole fraction ±0.001. The three systems satisfy the point-to-point thermodynamic consistency test. All the systems show positive deviations from ideality. The data have been correlated with the Margules, Van Laar, Wilson, NRTL and UNIQUAC equations.

UNIQUACChemistryGeneral Chemical EngineeringButanolGeneral Physics and AstronomyThermodynamicsMole fractionchemistry.chemical_compoundChlorobenzeneNon-random two-liquid modelIsobaric processVapor–liquid equilibriumPhysical and Theoretical Chemistry2-ButanolFluid Phase Equilibria
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Isobaric vapor–liquid equilibrium for binary mixtures of 1-hexene+n-hexane and cyclohexane+cyclohexene at 30, 60 and 101.3kPa

2009

Abstract Consistent vapor–liquid equilibria (VLE) data were determined for the binary systems 1-hexene + n-hexane and cyclohexane + cyclohexene at 30, 60 and 101.3 kPa, with the purpose of studying the influence of the pressure in the separation of these binary mixtures. The two systems show a small positive deviation from ideality and do not present an azeotrope. VLE data for the binary systems have been correlated by the Wilson, UNIQUAC and NRTL equations with good results and have been predicted by the UNIFAC group contribution method.

UNIQUACChemistryGeneral Chemical EngineeringGeneral Physics and AstronomyThermodynamicsGroup contribution methodchemistry.chemical_compoundHexeneAzeotropeNon-random two-liquid modelIsobaric processVapor–liquid equilibriumOrganic chemistryPhysical and Theoretical ChemistryUNIFACFluid Phase Equilibria
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Isobaric vapor-liquid equilibrium of binary mixtures of 1-propanol + chlorobenzene and 2-propanol + chlorobenzene

1997

Abstract Isobaric vapor-liquid equilibria were obtained for the system 1-propanol + chlorobenzene at 20 and 100 kPa and for the system 2-propanol + chlorobenzene at 100 kPa using a dynamic still. The experimental error in temperature was ±0.1 K, in pressure ±0.01 kPa and ±0.1 kPa for the experiments carried out at 20 and 100 kPa, respectively, and in the liquid and vapor mole fraction 0.001. The two systems satisfy the point-to-point thermodynamic consistency test. Both systems show a positive deviation from ideality. The data were well correlated with the Margules, Van Laar, Wilson, NRTL and UNIQUAC equations.

UNIQUACChemistryGeneral Chemical EngineeringGeneral Physics and AstronomyThermodynamicsMole fractionPropanolchemistry.chemical_compound1-PropanolChlorobenzeneNon-random two-liquid modelIsobaric processVapor–liquid equilibriumPhysical and Theoretical Chemistry
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Measurements and correlation of vapour–liquid equilibria of 2-butanone and hydrocarbons binary systems at two different pressures

2011

Abstract Consistent isobaric vapour–liquid equilibrium data have been measured for 2-butanone + n-hexane, 2-butanone + n-heptane, and 2-butanone + 2,2,4-trimethylpentane at two different pressures. All binary systems present a minimum boiling azeotrope at both pressures, and show that the azeotropic compositions are weakly dependent on pressure. The equilibrium data were correlated using the Wilson, NRTL, and UNIQUAC models for which the parameters are reported.

UNIQUACChemistryGeneral Chemical EngineeringGeneral Physics and AstronomyThermodynamicschemistry.chemical_compoundAzeotropeBoilingNon-random two-liquid modelIsobarIsobaric processBinary system224-TrimethylpentanePhysical and Theoretical ChemistryFluid Phase Equilibria
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Azeotropic distillation for 1-propanol dehydration with diisopropyl ether as entrainer: Equilibrium data and process simulation

2019

Abstract Azeotropic distillation process is widely used to separate non-ideal binary mixtures into their constituent pure components. 1-Propanol dehydration was used as case study and diisopropyl ether was analysed as possible entrainer in an azeotropic distillation. The separation of some alcohols from their aqueous solution is a challenging task because these aqueous mixture forms minimum boiling azeotrope. In this way, isobaric vapor-liquid and vapour-liquid-liquid equilibrium data were measured for the 1-propanol+ water + diisopropyl ether ternary mixture at 101.3 kPa. The data were correlated by NRTL and UNIQUAC models. A separation sequence (a decanter and a single-feed distillation c…

UNIQUACChemistryThermodynamicsFiltration and Separation02 engineering and technology021001 nanoscience & nanotechnologyAnalytical Chemistrychemistry.chemical_compound1-Propanol020401 chemical engineeringFractionating columnAzeotropic distillationAzeotropeNon-random two-liquid modelIsobaric processDiisopropyl ether0204 chemical engineering0210 nano-technologySeparation and Purification Technology
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Vapor–liquid equilibrium of binary mixtures of trichloroethylene with 1-pentanol, 2-methyl-1-butanol and 3-methyl-1-butanol at 100 kPa

1999

Abstract Isobaric vapor–liquid equilibria (VLE) have been obtained for the systems trichloroethylene+1-pentanol, trichloroethylene+2-methyl-1-butanol and trichloroethylene+3-methyl-1-butanol at 100 kPa using a dynamic still. The experimental error in temperature is ±0.1 K, in pressure ±0.1 kPa, and in the liquid and vapor mole fraction ±0.001. The three systems satisfy the point-to-point thermodynamic consistency test. All the systems show positive deviations from ideality. The data have been correlated with the Margules, van Laar, Wilson, NRTL and UNIQUAC equations.

UNIQUACChromatographyChemistryGeneral Chemical EngineeringButanolGeneral Physics and AstronomyThermodynamicsMole fractionGroup contribution methodchemistry.chemical_compoundAzeotropeNon-random two-liquid modelVapor–liquid equilibriumBinary systemPhysical and Theoretical ChemistryFluid Phase Equilibria
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Isobaric Vapor−Liquid Equilibrium in the Systems Methyl 1,1-Dimethylethyl Ether + 2-Methyl-2-propanol and Methyl 1,1-Dimethylethyl Ether + 2-Methylpe…

1999

Consistent vapor−liquid equilibrium data for the binary and ternary systems methyl 1,1-dimethylethyl ether (MTBE) + 2-methyl-2-propanol (TBA) and methyl 1,1-dimethylethyl ether (MTBE) + 2-methylpentane + 2-methyl-2-propanol (TBA) are reported at 101.3 kPa at temperatures in the range 328 to 356 K. The results indicate that the systems deviate positively from ideality and that no azeotrope is present. The activity coefficients of the solutions were correlated with composition by Wilson, NRTL, and UNIQUAC models. It is shown that the models allow a very good prediction of the phase equilibrium of the ternary system using the pertinent parameters of the binary system. In addition, the Wisniak−…

UNIQUACChromatographyTernary numeral system2-MethylpentaneGeneral Chemical EngineeringEtherGeneral ChemistryPropanolchemistry.chemical_compoundchemistryNon-random two-liquid modelVapor–liquid equilibriumPhysical chemistryBinary systemJournal of Chemical & Engineering Data
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