Thermodynamics Research Center / ThermoML | Fluid Phase Equilibria

Measurement and correlation of saturated liquid properties and gas solubility for decane, tetradecane and their binary mixtures saturated with carbon dioxide

Nourozieh, H.[Hossein], Kariznovi, M.[Mohammad], Abedi, J.[Jalal]
Fluid Phase Equilib. 2013, 337, 246-254
ABSTRACT
The solubilities of carbon dioxide (CO2) in decane, tetradecane and their binary mixtures have been measured at a temperature of 373.2 K and pressures up to 6 MPa using a rocking mechanism pressure volume temperature apparatus. The measurements presented in this paper were undertaken to determine the solubility and liquid saturated properties (density and viscosity) when a liquid hydrocarbon (decane, tetradecane and their mixtures) was saturated with CO2. The generated data for compositions and densities were correlated with the Soave- Redlich-Kwong and Peng-Robinson equations of state (EOSs). The binary interaction parameters were adjusted, and the volume translation technique was employed to correlate the experimental compositions and densities. The generated ternary data were correlated with the adjusted binary parameters from the data of binary pairs (CO2 + decane) and (CO2 + tetradecane). The calculated ternary compositions were found to be in good agreement with the experimental data using the binary parameters from the data of binary pairs for both EOSs. The results for the density of the saturated liquid phase indicated that volume translation should be applied to all components in the binary and ternary systems to accurately describe the saturated liquid densities for mixtures.
Compounds
# Formula Name
1 C10H22 decane
2 CO2 carbon dioxide
3 C14H30 tetradecane
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
  • 1
  • 2
  • Mole fraction - 2 ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Gas
  • Phase equilibration
  • 6
  • POMD
  • 1
  • 2
  • Mass density, kg/m3 ; Liquid
  • Mole fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Vibrating tube method
  • 6
  • POMD
  • 1
  • 2
  • Viscosity, Pa*s ; Liquid
  • Mole fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Moving piston method
  • 6
  • POMD
  • 2
  • 3
  • Mole fraction - 2 ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Gas
  • Phase equilibration
  • 6
  • POMD
  • 2
  • 3
  • Mass density, kg/m3 ; Liquid
  • Mole fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Vibrating tube method
  • 6
  • POMD
  • 2
  • 3
  • Viscosity, Pa*s ; Liquid
  • Mole fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Moving piston method
  • 6
  • POMD
  • 1
  • 2
  • 3
  • Mole fraction - 2 ; Liquid
  • Pressure, kPa; Liquid
  • Solvent: Mole fraction - 1; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Gas
  • Phase equilibration
  • 18
  • POMD
  • 1
  • 2
  • 3
  • Mass density, kg/m3 ; Liquid
  • Mole fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Solvent: Mole fraction - 1; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Vibrating tube method
  • 18
  • POMD
  • 1
  • 2
  • 3
  • Viscosity, Pa*s ; Liquid
  • Mole fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Solvent: Mole fraction - 1; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Moving piston method
  • 18
  • POMD
  • 1
  • 3
  • Mass density, kg/m3 ; Liquid
  • Pressure, kPa; Liquid
  • Mole fraction - 1; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Vibrating tube method
  • 55