Thermodynamics Research Center / ThermoML | Fluid Phase Equilibria

In situ Raman spectroscopic study of diffusion coefficients of methane in liquid water under high pressure and wide temperatures

Guo, H.[Huirong], Chen, Y.[Ying], Lu, W.[Wanjun], Li, L.[Lanlan], Wang, M.[Menghan]
Fluid Phase Equilib. 2013, 360, 274-278
ABSTRACT
Methane is commonly found in sedimentary basin at temperatures of at least 473 K. Accurate values of diffusion coefficients for methane in water at high pressure and elevated temperature are essential to our understanding of transport behavior of methane in pore spaces at reservoir conditions. However, the experimental data are limited to conditions at low temperatures and pressures. In this study, diffusion coefficients of methane in water were determined under high pressures (up to 40 MPa) and wide temperature range (from 273 K to 473 K) via Raman spectroscopic method. The relationship between diffusion coefficient of methane in water [D(CH4) in m2 /s] and temperature (T in K) was derived with Speedy-Angell power-law approach as: D(CH4)=D0[T/Ts-1]^m Where, D0= 15.95x10-9 m2 /s, Ts= 229.8 K, m=1.8769. At constant temperature, pressure has very small effect on the diffusion coefficients.
Compounds
# Formula Name
1 H2O water
2 CH4 methane
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
  • 2
  • 1
  • Binary diffusion coefficient, m2/s ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Mole fraction - 2; Liquid
  • Liquid
  • Time-dependent Raman spectra
  • 19