HR: 1340h
AN: B33C-1042 [Abstracts]
TI: Calcium carbonate precipitation along solution-solution interfaces in porous media
AU: * Redden, G D
EM: george.redden@inl.gov
AF: Idaho National Laboratory, PO Box 1625, MS 2208, Idaho Falls, ID 83415
United States
AU: Fang, Y
B33C-1042
AF: Pacific Northwest National Laboratory, Battelle Boulevard, MSIN: K9-33, Richland, WA 99352
United States
AU: Scheibe, T
EM: tim.scheibe@pnl.gov
AF: Pacific Northwest National Laboratory, Battelle Boulevard, MSIN: K9-33, Richland, WA 99352
United States
AU: Tartakovsky, A
EM: alexander.tartakovsky@pnl.gov
AF: Pacific Northwest National Laboratory, Battelle Boulevard, MSIN: K9-33, Richland, WA 99352
United States
AU: Fox, D T
EM: Don.Fox@inl.gov
AF: Idaho National Laboratory, PO Box 1625, MS 2208, Idaho Falls, ID 83415
United States
AU: White, T A
EM: Timothy.White@inl.gov
AF: Idaho National Laboratory, PO Box 1625, MS 2208, Idaho Falls, ID 83415
United States
AU: Fujita, Y
EM: yoshiko.fujita@inl.gov
AF: Idaho National Laboratory, PO Box 1625, MS 2208, Idaho Falls, ID 83415
United States
AU: Delwiche, M
EM: mark.delwiche@inl.gov
AF: Idaho National Laboratory, PO Box 1625, MS 2208, Idaho Falls, ID 83415
United States
AB:
Biogeochemical processes, such as mineral precipitation, microbial growth, or filtration of biological or mineral colloids,
can lead to localized solid deposition and changes in flow and permeability in porous media. The coupling between these
processes and flow depends on instantaneous flow paths, dispersive or diffusional mixing, localized flow velocities and the
kinetics of the biogeochemical reactions themselves. We have conducted experiments to help predict the outcome of this
coupling and how solids are, or could intentionally be, spatially distributed. Initial experiments have used calcium
carbonate precipitation in packed sand as a model system that has conceptual parallels to other biological and chemical
processes that generate mass in porous media. (A second experiment involves precipitate promotion via in situ urea
hydrolysis.) Parallel flowstreams of carbonate and calcium produce a mixing zone at the solution-solution interface by
diffusion and dispersion. The flowstreams have been created in both an annular geometry in a column, and in a 2-D flow cell.
X-ray tomography and color contrast methods are used to visualize the deposition process at the solution-solution
interface, and tracer analysis is used to analyze the systems for the evolution of heterogeneities and changes in
permeability. For the 2-D flow cell, continuum-scale modeling (using STORM, STOMP and Hydrogeochem codes) is used to
simulate the reactant concentration profiles along the interfacial mixing zone behavior prior to precipitation, a saturation
index profile, the changes in permeability that are induced as a consequence of precipitate deposition along the interface,
and the subsequent changes in how reactive solutes mix along the interface. The modeling goal is to link the continuum-scale
simulations to more detailed pore-scale simulations that are capable of representing the coupling between solute
concentrations, nucleation kinetics, precipitate growth kinetics, how precipitates fill pore spaces and how flow paths
changes with time. Smoothed Particle Hydrodynamics are being used for simulations at the pore scale. The intention is to
experimentally observe, and ultimately to control, how precipitates can be distributed in porous matrices.
DE: 0412 Biogeochemical kinetics and reaction modeling (0414, 0793, 1615, 4805, 4912)
DE: 0419 Biomineralization
DE: 0461 Metals
DE: 1009 Geochemical modeling (3610, 8410)
DE: 1847 Modeling
SC: Biogeosciences [B]
MN: Fall Meeting 2005