Thermodynamics and kinetics of methane hydrate formation and dissociation in presence of calcium carbonate

Huge amount of gas hydrate deposits are identified in deep marine sediments, which may be considered as a future source of energy. Since carbonate is one of the major components of marine sediments, in the present study attention has been given to characterize methane hydrate formation and dissociation in presence of calcium carbonate. Experiments were performed with 0%, 2%, 4%, 6% and 10% by weight of calcium carbonate in distilled water. Extensive investigations have been done on pressure-temperature equilibrium behavior of hydrate formation and dissociation at varying concentrations of calcium carbonate. Hydrate formation rate was found to vary with concentration of calcium carbonate as the solubility of calcium carbonate in water is controlled by the presence of simultaneous chemical equilibria involving a high number of species like Ca2+, CO32-, HCO3-, CO2, etc. Induction time for hydrate formation has also been measured at different concentrations of carbonate. Nucleation point for the hydrate formation was observed to be slightly higher at higher concentration of calcium carbonate due to increased heat absorption. Dissociation enthalpy of hydrates was calculated by using Clausius-Clapeyron at different measured conditions. Moles consumption of methane gas during hydrate formation at different concentrations of carbonate was measured using real gas equation and found to be minimum at 10 wt%. (C) 2018 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved.