Gernot Rother, Eugene S Ilton, Dirk Wallacher, Thomas Hauβ, Herbert T Schaef, Odeta Qafoku, Kevin M Rosso, Andrew R Felmy, Elizabeth G Krukowski, Andrew G Stack, Nico Grimm, Robert J Bodnar
Geochemistry and Interfacial Science Group, Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831-6110, United States. rotherg@ornl.gov
Environmental science & technology 2013 Jan 2Geologic storage of CO(2) requires that the caprock sealing the storage rock is highly impermeable to CO(2). Swelling clays, which are important components of caprocks, may interact with CO(2) leading to volume change and potentially impacting the seal quality. The interactions of supercritical (sc) CO(2) with Na saturated montmorillonite clay containing a subsingle layer of water in the interlayer region have been studied by sorption and neutron diffraction techniques. The excess sorption isotherms show maxima at bulk CO(2) densities of ≈ 0.15 g/cm(3), followed by an approximately linear decrease of excess sorption to zero and negative values with increasing CO(2) bulk density. Neutron diffraction experiments on the same clay sample measured interlayer spacing and composition. The results show that limited amounts of CO(2) are sorbed into the interlayer region, leading to depression of the interlayer peak intensity and an increase of the d(001) spacing by ca. 0.5 Å. The density of CO(2) in the clay pores is relatively stable over a wide range of CO(2) pressures at a given temperature, indicating the formation of a clay-CO(2) phase. At the excess sorption maximum, increasing CO(2) sorption with decreasing temperature is observed while the high-pressure sorption properties exhibit weak temperature dependence.
Gernot Rother, Eugene S Ilton, Dirk Wallacher, Thomas Hauβ, Herbert T Schaef, Odeta Qafoku, Kevin M Rosso, Andrew R Felmy, Elizabeth G Krukowski, Andrew G Stack, Nico Grimm, Robert J Bodnar. CO2 sorption to subsingle hydration layer montmorillonite clay studied by excess sorption and neutron diffraction measurements. Environmental science & technology. 2013 Jan 2;47(1):205-11
PMID: 22917276
View Full Text