Publication | Open Access
Clathrate hydrates in the system H2O–Ar at pressures and temperatures up to 30 kbar and 140 °C
43
Citations
20
References
1999
Year
High Hydrostatic PressureEngineeringExperimental ThermodynamicsClathrate HydratesChemistryNatural Gas HydrateSystem H2o–arChemical EngineeringPure ArgonPure Ice ViiThermodynamicsHigh Temperature GeochemistryMaterials ScienceChemical ThermodynamicsPhysical ChemistryHydrogenDecomposition CurveGas HydratePhysicochemical AnalysisPhase EquilibriumNatural Gas Hydrate SystemGeochemistryChemical Kinetics
Studies of the binary mixture H2O–Ar—by means of a quasi-isochoric scanning method—have revealed the range of stability of clathrate hydrates in the high-pressure and high-temperature region. The results obtained show an extension of the decomposition curve above the melting curve of pure argon and up to the melting curve of pure ice VII. At low pressures the argon decomposition temperature first increases and then decreases with pressure, showing a local maximum and minimum temperature. At higher pressures the slope of the decomposition curve remains positive but undergoes three more breaks. Two new quadruple points have been determined; at 105 °C, 20 kbar (Q4) and at 136 °C, 29 kbar (Q5). In the lower region (below 10 kbar) the decomposition curve shows two breaks; at 31.5 °C, 6.2 kbar (Q2) and at 37.5 °C, 9.6 kbar (Q3), indicating that three different clathrate structures are formed in this region. The positions of the three-phase lines separating the two clathrate structures at lower pressure could be obtained via Raman spectroscopy since the pressure and temperature dependence of the vibrational frequencies of the coupled O–H oscillations is different for each clathrate structure.
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