T174 Experimental, Field, and Modeling Studies of Geological Carbon Sequestration II
Tuesday, 29 October 2002
1:30 PM - 5:30 PM
REACTIVE TRANSPORT MODELING OF GEOLOGIC CO2 SEQUESTRATION
Paper number: T174-1
Program: Technical Sessions
Time: 1:30 PM – 1:45 PM
Authors
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John J. NitaoLawrence Livermore National Lab, Livermore, CA
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Carl I. SteefelLawrence Livermore National Lab, Livermore, CA
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Kevin G. KnaussLawrence Livermore National Lab, Livermore, CA
Abstract
Simulation results suggest that in the near-field environment of Sleipner-like settings roughly 85% by mass of injected CO2 remains and migrates as an immiscible fluid phase (subject to hydrodynamic and structural trapping), about 15% dissolves into formation waters (solubility trapping), and <1% precipitates as carbonate minerals (mineral trapping). Although seemingly negligible, mineral trapping has enormous strategic significance. We have identified four distinct mechanisms: siderite-magnesite precipitates within inter-bedded and cap-rock shales, dawsonite cementation occurs throughout the intra-aquifer plume, and siderite-magnesite-calcite rind forms along both lateral and upper plume boundaries. Local porosity and permeability are reduced by each of these mechanisms; however, such reduction is most extreme in clay-rich shales, owing to their relatively large Fe and Mg concentrations. In our 20-year simulations, initial porosity and permeability of the basal cap-rock shale have been reduced by 8% and 22%, respectively. Hence, the strategic significance of mineral trapping: it continuously improves seal integrity and therefore containment of the voluminous immiscible plume and solubility-trapped CO2.