Publications

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We develop a 2-D pore scale model of coupled fluid flow, reactive transport, and calcium carbonate (CaCO 3) precipitation and dissolution. The model is used to simulate transient experimental results of CaCO 3 precipitation and dissolution under supersaturated conditions in a microfluidic pore network (i.e., micromodel) in order to improve understanding of coupled reactive transport systems perturbed by geological CO 2 injection. In the micromodel, precipitation is induced by transverse mixing along the centerline in pore bodies. The reactive transport model includes the impact of pH upon carbonate speciation and a CaCO 3 reaction rate constant, the effect of changing reactive surface area upon the reaction, and the impact of pore blockage from CaCO 3 precipitation on diffusion and flow. Overall, the pore scale model qualitatively captured the precipitate morphology, precipitation rate, and maximum precipitation area using parameter values from the literature. In particular, we found that proper estimation of the effective diffusion coefficient (D eff) and the reactive surface area is necessary to adequately simulate precipitation and dissolution rates. In order to match the initial phase of fast precipitation, it was necessary to consider the top and bottom of the micromodel as additional reactive surfaces. In order to match a later phase when dissolution occurred, it was necessary to increase the dissolution rate compared to the precipitation rate, but the simulated precipitate area was still higher than the experimental results after ∼30 min, highlighting the need for future study. The model presented here allows us to simulate and mechanistically evaluate precipitation and dissolution of CaCO 3 observed in a micromodel pore network. This study leads to improved understanding of the fundamental physicochemical processes of CaCO 3 precipitation and dissolution under far-from-equilibrium conditions. Copyright 2012 by the American Geophysical Union.

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This document summarizes research performed under the SNL LDRD entitled - Computational Mechanics for Geosystems Management to Support the Energy and Natural Resources Mission. The main accomplishment was development of a foundational SNL capability for computational thermal, chemical, fluid, and solid mechanics analysis of geosystems. The code was developed within the SNL Sierra software system. This report summarizes the capabilities of the simulation code and the supporting research and development conducted under this LDRD. The main goal of this project was the development of a foundational capability for coupled thermal, hydrological, mechanical, chemical (THMC) simulation of heterogeneous geosystems utilizing massively parallel processing. To solve these complex issues, this project integrated research in numerical mathematics and algorithms for chemically reactive multiphase systems with computer science research in adaptive coupled solution control and framework architecture. This report summarizes and demonstrates the capabilities that were developed together with the supporting research underlying the models. Key accomplishments are: (1) General capability for modeling nonisothermal, multiphase, multicomponent flow in heterogeneous porous geologic materials; (2) General capability to model multiphase reactive transport of species in heterogeneous porous media; (3) Constitutive models for describing real, general geomaterials under multiphase conditions utilizing laboratory data; (4) General capability to couple nonisothermal reactive flow with geomechanics (THMC); (5) Phase behavior thermodynamics for the CO2-H2O-NaCl system. General implementation enables modeling of other fluid mixtures. Adaptive look-up tables enable thermodynamic capability to other simulators; (6) Capability for statistical modeling of heterogeneity in geologic materials; and (7) Simulator utilizes unstructured grids on parallel processing computers.

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Mercury intrusion porosimetry (MIP) is an often-applied technique for determining pore throat distributions and seal analysis of fine-grained rocks. Due to closure effects, potential pore collapse, and complex pore network topologies, MIP data interpretation can be ambiguous, and often biased toward smaller pores in the distribution. We apply 3D imaging techniques and lattice-Boltzmann modeling in interpreting MIP data for samples of the Cretaceous Selma Group Chalk. In the Mississippi Interior Salt Basin, the Selma Chalk is the apparent seal for oil and gas fields in the underlying Eutaw Fm., and, where unfractured, the Selma Chalk is one of the regional-scale seals identified by the Southeast Regional Carbon Sequestration Partnership for CO2 injection sites. Dual focused ion - scanning electron beam and laser scanning confocal microscopy methods are used for 3D imaging of nanometer-to-micron scale microcrack and pore distributions in the Selma Chalk. A combination of image analysis software is used to obtain geometric pore body and throat distributions and other topological properties, which are compared to MIP results. 3D data sets of pore-microfracture networks are used in Lattice Boltzmann simulations of drainage (wetting fluid displaced by non-wetting fluid via the Shan-Chen algorithm), which in turn are used to model MIP procedures. Results are used in interpreting MIP results, understanding microfracture-matrix interaction during multiphase flow, and seal analysis for underground CO2 storage.

Dissolved CO2 from geological CO2 sequestration may react with dissolved minerals in fractured rocks or confined aquifers and cause mineral precipitation. The overall rate of reaction can be limited by diffusive or dispersive mixing, and mineral precipitation can block pores and further hinder these processes. Mixing-induced calcite precipitation experiments were performed by injecting solutions containing CaCl2 and Na2CO3 through two separate inlets of a micromodel (1-cm x 2-cm x 40-microns); transverse dispersion caused the two solutions to mix along the center of the micromodel, resulting in calcite precipitation. The amount of calcite precipitation initially increased to a maximum and then decreased to a steady state value. Fluorescent microscopy and imaging techniques were used to visualize calcite precipitation, and the corresponding effects on the flow field. Experimental micromodel results were evaluated with pore-scale simulations using a 2-D Lattice-Boltzmann code for water flow and a finite volume code for reactive transport. The reactive transport model included the impact of pH upon carbonate speciation and calcite dissolution. We found that proper estimation of the effective diffusion coefficient and the reaction surface area is necessary to adequately simulate precipitation and dissolution rates. The effective diffusion coefficient was decreased in grid cells where calcite precipitated, and keeping track of reactive surface over time played a significant role in predicting reaction patterns. Our results may improve understanding of the fundamental physicochemical processes during CO2 sequestration in geologic formations.

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