Thermodynamics Research Center / ThermoML | Fluid Phase Equilibria

Limiting activity coefficient measurements in binary mixtures of dichloromethane and 1-alkanols (C1 - C4)

Vrbka, P.[Pavel], Dohnal, V.[Vladimir]
Fluid Phase Equilib. 2016, 411, 59-65
ABSTRACT
Limiting activity coefficients in binary mixtures of dichloromethane with four lower 1-alkanols (C1 - C4) were experimentally determined employing alternatively the techniques of inert gas stripping, comparative ebulliometry, Rayleigh distillation, and differential distillation. For each case, the suitable technique was chosen on the basis of the limiting relative volatility of the solute and/or volatility of the solvent. The measurements yielding data of good accuracy (relative standard uncertainty of limiting activity coefficients from 0.01 to 0.03) were carried out at several temperatures in the range from (283 - 333) K. The variation of limiting activity coefficients with temperature was fitted by a suitable two- or three-parameter equation and compared with available literature information on both limiting activity coefficients and calorimetric partial molar excess enthalpies at infinite dilution. The performance of the leading prediction method Modified UNIFAC was further examined using these new data. Concentration dependences of activity coefficients calculated from their infinite dilution values using van Laar equation were found to agree well with those inferred from reliable VLE data from the literature. The occurrence of an azeotropic point was tested for the systems under study and the temperature dependence of the azeotropic composition was estimated for mixtures of dichloromethane with methanol and ethanol.
Compounds
# Formula Name
1 CH4O methanol
2 C2H6O ethanol
3 C3H8O propan-1-ol
4 C4H10O butan-1-ol
5 CH2Cl2 dichloromethane
Datasets
The table above is generated from the ThermoML associated json file (link above). POMD and RXND refer to PureOrMixture and Reaction Datasets. The compound numbers are included in properties, variables, and phases, if specificied; the numbers refer to the table of compounds on the left.
Type Compound-# Property Variable Constraint Phase Method #Points
  • POMD
  • 5
  • Vapor or sublimation pressure, kPa ; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Gas
  • Ebulliometric method (Recirculating still)
  • 14
  • POMD
  • 1
  • 5
  • Activity coefficient - 5 ; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 5; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Rayleigh distillation
  • 5
  • POMD
  • 1
  • 5
  • Activity coefficient - 1 ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 1; Liquid
  • Liquid
  • comparative ebulliometry
  • 3
  • POMD
  • 2
  • 5
  • Activity coefficient - 5 ; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 5; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Rayleigh distillation
  • 5
  • POMD
  • 2
  • 5
  • Activity coefficient - 2 ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 2; Liquid
  • Liquid
  • comparative ebulliometry
  • 3
  • POMD
  • 3
  • 5
  • Activity coefficient - 5 ; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 5; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Inert gas stripping
  • 6
  • POMD
  • 3
  • 5
  • Activity coefficient - 5 ; Liquid
  • Mole fraction - 5; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Rayleigh distillation
  • 1
  • POMD
  • 3
  • 5
  • Activity coefficient - 3 ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 3; Liquid
  • Liquid
  • comparative ebulliometry
  • 3
  • POMD
  • 4
  • 5
  • Activity coefficient - 5 ; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 5; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • inert gas stripping
  • 6
  • POMD
  • 4
  • 5
  • Activity coefficient - 4 ; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 4; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • differential distillation
  • 3