Thermodynamics Research Center / ThermoML | Fluid Phase Equilibria

High-pressure experimental vapour-liquid-liquid equilibrium measurements and modelling for natural gas processing: Equipment validation, and the system CH4 + nC6H14 + H2O

Kruger, Francois, Varsos, Athanasios A., Kontogeorgis, Georgios M., Solms, Nicolas von
Fluid Phase Equilib. 2019, 501, 112276
ABSTRACT
Despite its relevance for oil and gas separation processes, surprisingly few experimental three-phase data are available in the open literature for gas-condensate-water systems. In support of proposed subsea processing facilities, a three-phase equilibrium measurement apparatus has been recommissioned for the measurement of C1 + nC6 + H2O systems between 303 and 323 K. The apparatus has been validated by comparison with literature VLE data for C1 + H2O and C1 + nC6, with the experimental uncertainty estimated at +- 9% (95% confidence interval). 81 new three-phase C1 + nC6 + H2O data points have been generated for three different feed mixtures. The relative compositions in each phase are strongly correlated to the experimental feed composition, while the solubility-temperature trends indicate complex interactions in the system. The repeatability of the measurements ranges from below 1% for major components up to 10 - 20% for trace components in the respective phases. Experimental standard deviations are comparable with those reported for literature data. The data have been modelled using the CPA and sPC-SAFT equations of state. Satisfactory results were achieved for major components (accuracy between 1 and 6%), while order of magnitude errors were observed for certain trace components (e.g. water in the HC-rich phase). Overall, sPC-SAFT provided slightly better predictions compared to the CPA, but the differences are rather modest.
Compounds
# Formula Name
1 CH4 methane
2 C6H14 hexane
3 H2O water
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
  • 3
  • Mole fraction - 3 ; Liquid mixture 1
  • Mole fraction - 3 ; Gas
  • Mole fraction - 1 ; Gas
  • Temperature, K; Gas
  • Pressure, kPa; Gas
  • Mole fraction - 1; Liquid mixture 1
  • Liquid mixture 1
  • Gas
  • Chromatography
  • Chromatography
  • Chromatography
  • 9
  • POMD
  • 1
  • 2
  • 3
  • Mole fraction - 2 ; Liquid mixture 2
  • Mole fraction - 3 ; Gas
  • Mole fraction - 2 ; Gas
  • Temperature, K; Gas
  • Pressure, kPa; Gas
  • Mole fraction - 3; Liquid mixture 2
  • Liquid mixture 2
  • Gas
  • Chromatography
  • Chromatography
  • Chromatography
  • 9
  • POMD
  • 1
  • 2
  • 3
  • Mole fraction - 2 ; Liquid mixture 2
  • Mole fraction - 2 ; Liquid mixture 1
  • Mole fraction - 1 ; Liquid mixture 1
  • Temperature, K; Liquid mixture 1
  • Pressure, kPa; Liquid mixture 1
  • Mole fraction - 1; Liquid mixture 2
  • Liquid mixture 2
  • Liquid mixture 1
  • Chromatography
  • Chromatography
  • Chromatography
  • 9