Thermodynamic and hydrodynamic constraints on overpressure caused by hydrate dissociation: A porescale model

Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. [1] It has been suggested that volume expansion caused by hydrate dissociation in sediment pores can result in large overpressure, which in turn may destabilize the sediment and trigger massive submarine landslides. Here, we investigate the pressure evolution during thermally‐induced dissociation, by means of a pore‐scale model that couples dissociation kinetics, multiphase flow and geomechanics. Dissociation is controlled by a self‐preservation mechanism: increasing pore pressure reduces the driving force for dissociation. Hence, the overpressure is constrained by the phase equilibrium pressure, regardless of the kinetic rate of dissociation, heat supply, and sediment permeability. Furthermore, we find that the timescale for buildup of pressure by dissociation is typically much larger than that for its dissipation by drainage. Consequently, the overpressure is controlled by the capillary entry thresholds, which depend on the mode of gas invasion. In low‐permeability systems, fracturing is the preferred mechanism, occurring at capillary pressures lower than the entry thresholds in the undeformed sediment. Our results suggest that while large overpressures cannot be sustained by rapid dissociation in natural systems, dissociation can induce important geomechanical effects. Gas migration by fracturing provides a possible link between dissociation, sediment deformation and methane venting.dynamic and hydrodynamic constraints on overpressure caused by hydrate dissociation: A pore‐scale model, Geophys.