Permanent Carbon Dioxide Storage in Deep-Sea Sediments
Stabilizing the concentration of atmospheric CO₂ may require storing enormous quantities of captured anthropogenic CO₂ in near-permanent geologic reservoirs. Because of the subsurface temperature profile of terrestrial storage sites, CO₂ stored in these reservoirs is buoyant. As a result, a portion...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2006-08, Vol.103 (33), p.12291-12295 |
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Sprache: | eng |
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Zusammenfassung: | Stabilizing the concentration of atmospheric CO₂ may require storing enormous quantities of captured anthropogenic CO₂ in near-permanent geologic reservoirs. Because of the subsurface temperature profile of terrestrial storage sites, CO₂ stored in these reservoirs is buoyant. As a result, a portion of the injected CO₂ can escape if the reservoir is not appropriately sealed. We show that injecting CO₂ into deep-sea sediments >3,000-m water depth and a few hundred meters of sediment provides permanent geologic storage even with large geomechanical perturbations. At the high pressures and low temperatures common in deep-sea sediments, CO₂ resides in its liquid phase and can be denser than the overlying pore fluid, causing the injected CO₂ to be gravitationally stable. Additionally, CO₂ hydrate formation will impede the flow of CO₂(l) and serve as a second cap on the system. The evolution of the CO₂ plume is described qualitatively from the injection to the formation of CO₂ hydrates and finally to the dilution of the CO₂(aq) solution by diffusion. If calcareous sediments are chosen, then the dissolution of carbonate host rock by the CO₂(aq) solution will slightly increase porosity, which may cause large increases in permeability. Karst formation, however, is unlikely because total dissolution is limited to only a few percent of the rock volume. The total CO₂ storage capacity within the 200-mile economic zone of the U.S. coastline is enormous, capable of storing thousands of years of current U.S. CO₂ emissions. |
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ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.0605318103 |