A flow‐through experiment was performed to investigate evolution of a fractured carbonate caprock during flow of CO2‐acidified brine. A core was taken from the Amherstburg limestone, a caprock formation overlying the Bois Blanc and Bass Islands formations, which have been used to demonstrate CO2 storage in the Michigan basin. The inlet brine was representative of deep saline brines saturated with CO2, resulting in a starting pH of 4.4. Experimental conditions were 27 °C and 10 MPa. X‐ray computed tomography and scanning electron microscopy were used to observe evolution of fracture geometry and to investigate mineralogical changes along the fracture surface. The initial brine flow corresponded to an average fluid velocity of 110 cm hr−1. After one week, substantial mineral dissolution caused the average cross‐sectional area of the fracture to increase from 0.09 cm2 to 0.24 cm2. This demonstrates that carbonate caprocks, if fractured, can erode quickly and may jeopardize sealing integrity when hydrodynamic conditions promote flow of CO2‐acidified brine. However, changes to fracture permeability due to mineral dissolution may be offset by unaltered constrictions along the flow path and by increases in surface roughness. In this experiment, preferential dissolution of calcite over dolomite led to uneven erosion of the fracture surface and an increase in roughness. In areas with clay minerals, calcite dissolution left behind a silicate mineral‐rich microporous coating along the fracture wall. Thus, the evolution of fracture permeability will depend in a complex way on the carbonate content, as well as the heterogeneity of the minerals and their spatial patterning. © 2011 Society of Chemical Industry and John Wiley & Sons, Ltd
A single-sided transient plane source technique has been used to determine the thermal conductivity and thermal diffusivity of a compacted methane hydrate sample over the temperature range of 261.5-277.4 K and at gas-phase pressures ranging from 3.8 to 14.2 MPa. The average thermal conductivity, 0.68 +/- 0.01 W/(m K), and thermal diffusivity, 2.04 x 10(-7) +/- 0.04 x 10(-7) m2/s, values are, respectively, higher and lower than previously reported values. Equilibrium molecular dynamics (MD) simulations of methane hydrate have also been performed in the NPT ensemble to estimate the thermal conductivity for methane compositions ranging from 80 to 100% of the maximum theoretical occupation, at 276 K and at pressures ranging from 0.1 to 100 MPa. Calculations were performed with three rigid potential models for water, namely, SPC/E, TIP4P-Ew, and TIP4P-FQ, the last of which includes the effects of polarizability. The thermal conductivities predicted from MD simulations were in reasonable agreement with experimental results, ranging from about 0.52 to 0.77 W/(m K) for the different potential models with the polarizable water model giving the best agreement with experiments. The MD simulation method was validated by comparing calculated and experimental thermal conductivity values for ice and liquid water. The simulations were in reasonable agreement with experimental data. The simulations predict a slight increase in the thermal conductivity with decreasing methane occupation of the hydrate cages. The thermal conductivity was found to be essentially independent of pressure in both simulations and experiments. Our experimental and simulation thermal conductivity results provide data to help predict gas hydrate stability in sediments for the purposes of production or estimating methane release into the environment due to gradual warming.
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