Search results for "Efficient"

showing 10 items of 1603 documents

Phase equilibria in the systems 3-methylpentane + methylcyclohexane, diisopropyl ether + methylcyclohexane and 3-methylpentane + diisopropyl ether + …

2002

Abstract Consistent vapor–liquid equilibria (VLE) at 101.3 kPa has been determined for the ternary system 3-methylpentane+diisopropyl ether (DIPE)+methylcyclohexane and the binary subsystems 3-methylpentane+methylcyclohexane and DIPE+methylcyclohexane in the temperature range from 336 to 374 K. According to the experimental results, the systems exhibit slight positive deviation from ideal behavior and no azeotrope is present. The VLE data have been correlated with the composition using the Wilson, UNIQUAC and NRTL relations. These models allow good prediction of the VLE properties of the ternary system from those of the pertinent binary subsystems.

Activity coefficientUNIQUACTernary numeral systemGeneral Chemical EngineeringGeneral Physics and AstronomyThermodynamicschemistry.chemical_compoundchemistryAzeotropeNon-random two-liquid modelDiisopropyl etherPhysical and Theoretical ChemistryMethylcyclohexane3-MethylpentaneFluid Phase Equilibria
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Vapor–liquid equilibria in the ternary system isobutyl alcohol+isobutyl acetate+butyl propionate and the binary systems isobutyl alcohol+butyl propio…

2005

Abstract Consistent vapor–liquid equilibrium (VLE) data at 101.3 kPa have been determined for the ternary system isobutyl alcohol (IBA) + isobutyl acetate (IBAc) + butyl propionate (BUP) and two constituent binary systems: IBA + BUP and IBAc + BUP. The IBA + BUP system show lightly positive deviation from Raoult's law and IBAc + BUP system exhibits no deviation from ideal behaviour. The activity coefficients of the solutions were correlated with its composition by the Wilson, NRTL, UNIQUAC models. The ternary system is very well predicted from binary interaction parameters. BUP eliminates the IBA–IBAc binary azeotrope. The change of phase equilibria behaviour is significant therefore this s…

Activity coefficientUNIQUACTernary numeral systemIsobutyl acetateChemistryGeneral Chemical EngineeringGeneral Physics and AstronomyThermodynamicschemistry.chemical_compoundAzeotropeNon-random two-liquid modelOrganic chemistryBinary systemPhysical and Theoretical ChemistryUNIFACFluid Phase Equilibria
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Vapor–liquid equilibria in the systems 3-methylpentane+methyl 1,1-dimethylethyl ether and 3-methylpentane+methyl 1,1-dimethylpropyl ether at 101.3 kPa

1999

Abstract Pure-component vapor pressure of 3-methylpentane and vapor–liquid equilibrium (VLE) for the binary systems of 3-methylpentane with methyl 1,1-dimethylethyl ether (MTBE) and with methyl 1,1-dimethylpropyl ether (TAME) at 101.3 kPa have been measured. Both systems exhibit small positive deviations from ideality. They can be described as regular solutions and do not present azeotrope. The activity coefficients and boiling points of the solutions were correlated with its composition by Wilson, UNIQUAC, NRTL, and Wisniak–Tamir equations.

Activity coefficientUNIQUACVapor pressureGeneral Chemical EngineeringGeneral Physics and AstronomyEtherchemistry.chemical_compoundBoiling pointchemistryAzeotropeNon-random two-liquid modelPhysical chemistryOrganic chemistryPhysical and Theoretical Chemistry3-MethylpentaneFluid Phase Equilibria
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Vapor−Liquid Equilibria for the Binary Systems tert-Butyl Alcohol + Toluene, + Isooctane, and + Methylcyclohexane at 101.3 kPa

1998

Vapor-liquid equilibria were measured for binary systems of tert-butyl alcohol with toluene, isooctane, and methylcyclohexane at 101.3 kPa using a recirculating still. Experimental values of the vapor pressure of non-oxygenated pure components have been obtained. The accuracy of experimental measurements was ±0.01 K in temperature, ±0.01 kPa in pressure, and ±0.001 in mole fractions. The results are thermodynamically consistent according to the point-to-point consistency test. The data were correlated with five liquid-phase activity coefficients models (Margules, Van Laar, Wilson, NRTL, UNIQUAC).

Activity coefficientUNIQUACVapor pressureGeneral Chemical EngineeringThermodynamicsGeneral ChemistryTolueneGroup contribution methodchemistry.chemical_compoundchemistryNon-random two-liquid modelOrganic chemistryBinary systemMethylcyclohexaneJournal of Chemical & Engineering Data
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Binding of a fluorescent dansylcadaverine-substance P analogue to negatively charged phospholipid membranes.

2000

Abstract We have investigated the binding of a new dansylcadaverine derivative of substance P (DNC-SP) with negatively charged small unilamellar vesicles composed of a mixture of phosphatidylcholine (PC) and either phosphatidylglycerol (PG) or phosphatidylserine (PS) using fluorescence spectroscopic techniques. The changes in fluorescence properties were used to obtain association isotherms at variable membrane negative charges and at different ionic strengths. The experimental association isotherms were analyzed using two binding approaches: (i) the Langmuir adsorption isotherm and the partition equilibrium model, that neglect the activity coefficients; and (ii) the partition equilibrium m…

Activity coefficientVesicleLipid BilayersAnalytical chemistryLangmuir adsorption modelCharge densityGeneral MedicineSubstance PBiochemistryBinding constantFluorescencechemistry.chemical_compoundsymbols.namesakeMembranechemistryModels ChemicalStructural BiologyPhosphatidylcholinePartition equilibriumCadaverinesymbolsMolecular BiologyPhospholipidsFluorescent DyesProtein BindingInternational journal of biological macromolecules
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Thermodynamic properties and conductivities of some dodecylsurfactants in water

1988

Densities, heat capacities, enthalpies of dilution, osmotic coefficients and conductivities are reported for dodecylamine hydrochloride, dodecyldimethylammonium and dodecyltrimethylammonium chloride in water over a wide range of concentration. The last two properties were also measured for dodecyltrimethylammonium bromide. From the thermodynamic data partial molar volumes, heat capacities and relative enthalpies and nonideal free energies and entropies were derived as a function of the surfactant concentration. The cmc's and degree of counterion dissociation were also calculated from the transport properties. It is shown that the trends of volumes, enthalpies, free energies and entropies ar…

Activity coefficientchemistry.chemical_classificationQuantitative Biology::BiomoleculesAqueous solutionInorganic chemistryThermodynamics of micellizationBiophysicsThermodynamicsBiochemistryMicelleDissociation (chemistry)DilutionCondensed Matter::Soft Condensed MatterchemistryPulmonary surfactantPhysics::Chemical PhysicsPhysical and Theoretical ChemistryCounterionMolecular BiologyJournal of Solution Chemistry
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Isobaric Vapor−Liquid Equilibria for Binary and Ternary Mixtures of Dipropyl Ether, 1-Propyl Alcohol, and Butyl Propionate

2006

Consistent vapor−liquid equilibrium (VLE) data at 101.3 kPa have been determined for the ternary system dipropyl ether + 1-propyl alcohol + butyl propionate and two constituent binary systems:  dipropyl ether + butyl propionate and 1-propyl alcohol + butyl propionate. The dipropyl ether + butyl propionate system exhibits ideal behavior, and the 1-propyl alcohol + butyl propionate system shows positive deviations from Raoult's law. No additional azeotropes are present. The activity coefficients of the solutions were correlated with its composition by the Wilson, NRTL, and UNIQUAC models. The ternary system is well-predicted from binary interaction parameters. Butyl propionate breaks the dipr…

Activity coefficientchemistry.chemical_classificationUNIQUACTernary numeral systemGeneral Chemical EngineeringRaoult's lawEtherGeneral ChemistryMedicinal chemistrychemistry.chemical_compoundchemistryAzeotropeNon-random two-liquid modelPropionateOrganic chemistryJournal of Chemical & Engineering Data
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Phase Equilibrium for the Esterification Reaction of Acetic Acid + Butan-1-ol at 101.3 kPa

2007

In this work, the thermodynamic behavior of catalytic esterification reaction equilibrium and vapor–liquid equilibria (VLE) for the quaternary reactive system acetic acid + butan-1-ol + butyl acetate + water and constituent binary systems acetic acid + butyl acetate, butan-1-ol + butyl acetate, and butan-1-ol + water have been determined at 101.3 kPa, and liquid–liquid equilibria (LLE) of the binary system butan-1-ol + water have also been determined. The esterification reaction rate of the acetic acid and butan-1-ol mixture is very slow. So, in this study, p-toluenesulfonic acid was selected as the catalyst to accelerate the chemical reaction. The measured VLE data were correlated by the N…

Activity coefficientchemistry.chemical_compoundAcetic acidUNIQUACChemistryGeneral Chemical EngineeringNon-random two-liquid modelOrganic chemistryGeneral ChemistryBinary systemButyl acetateChemical reactionCatalysisJournal of Chemical & Engineering Data
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Isobaric Vapor−Liquid Equilibria of Trichloroethylene with 1-Butanol and 2-Butanol at 20 and 100 kPa

1996

Vapor−liquid equilibria for trichloroethylene + 1-butanol, and + 2-butanol are reported at 20 and 100 kPa. The two systems satisfy the point-to-point thermodynamic consistency test. Both systems show a positive deviation from ideality.

Activity coefficientchemistry.chemical_compoundBoiling pointchemistryTrichloroethyleneGeneral Chemical EngineeringAzeotropeButanolIsobaric processThermodynamicsGeneral ChemistryBinary system2-ButanolJournal of Chemical & Engineering Data
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1-Ethyl-3-methylimidazolium Dicyanamide as a Very Efficient Entrainer for the Extractive Distillation of the Acetone + Methanol System

2012

Isobaric vapor–liquid equilibria (VLE) for the ternary system acetone + methanol +1-ethyl-3-methylimidazolium dicyanamide ([emim][DCA]) as well as the two solvent + IL binary systems have been obtained at 100 kPa using a recirculating still. The addition of [emim][DCA] to the solvent mixture produced a salting-out effect greater than that produced by other ionic liquids, showing that this ionic liquid is, until now, the best IL tested as an entrainer for the extractive distillation of the acetone + methanol mixtures, causing the azeotrope to disappear for an ionic liquid mole fraction as low as 0.031, at 100 kPa. This behavior can be explained on the basis of the influence of the IL concent…

Activity coefficientchemistry.chemical_compoundTernary numeral systemChemistryGeneral Chemical EngineeringAzeotropeInorganic chemistryIonic liquidAcetoneNon-random two-liquid modelExtractive distillationGeneral ChemistryDicyanamideJournal of Chemical & Engineering Data
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