Comparison of the Performance of Different Thermodynamic Models for Liquid Phase in Predicting the Phase Behavior of Hydrogen Hydrates with THF

In this work, five different thermodynamic models for correlating the fugacity of water and tetrahydrofuran (thf) in liquid phase in equilibrium with hydrogen hydrate phase, based on the van der waals–platteeuw (vdw-p) statistical thermodynamic model are used and the equilibrium pressures of hydrogen hydrate at different temperatures are calculated. the dissociation pressure of binary hydrogen hydrates is determined by using the zele–lee–holder cavity distortion model. the studied models in liquid phase are nrtl excess gibbs energy, peng-robinson (pr) equation of state (pr eos), peng-robinson-steryjek-vera eos with the wong-sandler mixing rule (prsv-ws), dashtizadeh eos (dptg), and ghotbi-vera simple saft (gv-ssaft) eos. the results show that the gv-ssaft model correlates more accurately the experimental dissociation pressure of binary hydrogen hydrate. additionally, hydrogen storage capacity of binary hydrogen hydrates is calculated.