2008 Joint Meeting of The Geological Society of America, Soil Science Society of America, American Society of Agronomy, Crop Science Society of America, Gulf Coast Association of Geological Societies with the Gulf Coast Section of SEPM

Paper No. 9
Presentation Time: 10:15 AM

Back to Basics: The Importance of the Carbonate Buffer in Multi-Phase (CO2-H2O) Water-Rock Systems - Critical Considerations for Predictions, Experiments and Field Applications


NEWELL, Dennis L., Earth and Environmental Sciences, Los Alamos National Laboratory, Mail Stop J514, Los Alamos, NM 87545, KASZUBA, John, Earth and Environmental Sciences, Los Alamos National Laboratory, Mail Stop J514, Los Alamos, NM 87545-0001, VISWANATHAN, Hari, Earth and Environmental Sciences, Los Alamos National Laboratory, MS T003, Los Alamos, NM 87545, SÁNCHEZ, Alicia, Chevron Energy Technology Co, care of Los Alamos National Laboratory, Mail Stop J514, Los Alamos, NM 87545 and MAZZOLENI, Lynn, Earth and Environmental Sciences, Los Alamos National Laboratory, Mail Stop D469, Los Alamos, NM 87545, dnewell@lanl.gov

In CO2-bearing water-rock systems, incomplete characterization and definition of groundwater can lead to erroneous predictions of rock-water interactions. In particular, speciation, pH and mineral saturation can be very sensitive to natural bicarbonate buffer in groundwater. A 2% error in identifying initial bicarbonate content of groundwater, prior to adding anthropogenic CO2, could produce as much as a 1 pH unit error when calculating in-situ pH. Such an error greatly affects calculation of saturation indices of carbonates, for example, predicting mineral dissolution when in fact carbonates are precipitating. In closed system laboratory experiments, we recreate the geochemical conditions of a multi-phase fluid-rock basin at steady state, wherein brine, rock, and immiscible supercritical CO2 coexist. We define key parameters that need to be measured in the fluid to accurately model these systems and demonstrate how to use these data with off-the-shelf geochemical codes to accurately predict experimental results. One set of experiments evaluates the sensitivity of dawsonite saturation at 75oC and 200 bar in 1 molal NaCl brine + albite + supercritical CO2. Initial bicarbonate in this simple system is constrained by equilibrium with atmospheric CO2 and final bicarbonate (1.325 molal) is measured by coulometric titration. Dawsonite is undersaturated in both experiment and calculation, and dawsonite solubility is not sensitive to initial bicarbonate. In contrast, using previously published experimental data (5.5 molal NaCl brine, arkosic sandstone, shale, and supercritical CO2 at 200oC and 200 bars, Kaszuba et al., 2005), we demonstrate that calculated siderite and magnesite saturation and pH are sensitive to initial bicarbonate. Siderite and magnesite are undersaturated when using near-zero initial bicarbonate and oversaturated when using 20 mmolal initial bicarbonate in calculations. Our findings are critical for predictions, field monitoring and measurement, and verification of enhanced oil recovery, in-situ oil shale production, and geologic sequestration of CO2.