106 research outputs found

    Water in minerals? A peak in the infrared

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    The study of water in minerals with infrared spectroscopy is reviewed with emphasis on natural and synthetic quartz. Water can be recognized in minerals as fluid inclusions and as isolated molecules and can be distinguished from hydroxide ion. The distinction between very small inclusions and aggregates of structurally bound molecules is difficult. New studies of synthetic quartz using near-infrared spectroscopy are reported. These demonstrate that water molecules are the dominant hydrogen containing species in synthetic quartz but that this water is not in aggregates large enough to form ice when cooled

    Solubility and diffusional uptake of hydrogen in quartz at high water pressures: Implications for hydrolytic weakening

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    Attempts to introduce molecular water into dry, natural quartz crystals by diffusive transport and thus weaken them hydrolytically at T = 700°–900°C and PH_2O = 400–1550 MPa have failed. Infrared spectroscopy of hydrothermally annealed single crystals of natural quartz reveals the diffusive uptake of interstitial hydrogen (resulting in hydroxyl groups) at rates similar to those previously proposed for intracrystalline water at high water pressures. The solubility of interstitial hydrogen at these conditions is independent of temperature and pressure; instead, it depends upon the initial aluminum concentration by the local charge neutrality condition [H_i·] = [Al_(Si)′]. The rate of interstitial hydrogen diffusion parallel to c is given by an Arrhenius relation with D_0 = 1.4 × 10^(−1) m^2/s and Q = 200 ± 20 kJ/mol, in close agreement with H diffusivities reported for much lower pressures (PH_2O = 2.5 MPa). Deformation experiments following hydrothermal annealing show no mechanical weakening, and the lack of any detectable broadband absorption associated with molecular water shows that the diffusion rates of structural water are much lower than those of hydrogen. These results are consistent with the available oxygen diffusion data for quartz and with the failure to observe weakening in previous studies of quartz deformation at pressures of 300–500 MPa; they call into question the rapid rates of diffusion originally suggested for the hydrolytic weakening defect. It is suggested that the observed weakening in many previous experiments was complicated by microcracking processes in response to nonhydrostatic stresses and low effective confining pressures. Extensive microcracking may provide a mechanism for molecular water to enter quartz and allow local plastic deformation to occur. It does not appear that molecular water can diffuse far enough into uncracked quartz to allow hydrolytic weakening over annealing times that are feasible in the laboratory

    Integrated Geothermal-CO2 Reservoir Systems: Reducing Carbon Intensity through Sustainable Energy Production and Secure CO2 Storage

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    AbstractLarge-scale geologic CO2 storage (GCS) can be limited by overpressure, while geothermal energy production is often limited by pressure depletion. We investigate how synergistic integration of these complementary systems may enhance the viability of GCS by relieving overpressure, which reduces pore-space competition, the Area of Review, and the risks of CO2 leakage and induced seismicity, and by producing geothermal energy and water, which can defray parasitic energy and water costs of CO2 capture

    Geochemical detection of carbon dioxide in dilute aquifers

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    <p>Abstract</p> <p>Background</p> <p>Carbon storage in deep saline reservoirs has the potential to lower the amount of CO<sub>2 </sub>emitted to the atmosphere and to mitigate global warming. Leakage back to the atmosphere through abandoned wells and along faults would reduce the efficiency of carbon storage, possibly leading to health and ecological hazards at the ground surface, and possibly impacting water quality of near-surface dilute aquifers. We use static equilibrium and reactive transport simulations to test the hypothesis that perturbations in water chemistry associated with a CO<sub>2 </sub>gas leak into dilute groundwater are important measures for the potential release of CO<sub>2 </sub>to the atmosphere. Simulation parameters are constrained by groundwater chemistry, flow, and lithology from the High Plains aquifer. The High Plains aquifer is used to represent a typical sedimentary aquifer overlying a deep CO<sub>2 </sub>storage reservoir. Specifically, we address the relationships between CO<sub>2 </sub>flux, groundwater flow, detection time and distance. The CO<sub>2 </sub>flux ranges from 10<sup>3 </sup>to 2 × 10<sup>6 </sup>t/yr (0.63 to 1250 t/m<sup>2</sup>/yr) to assess chemical perturbations resulting from relatively small leaks that may compromise long-term storage, water quality, and surface ecology, and larger leaks characteristic of short-term well failure.</p> <p>Results</p> <p>For the scenarios we studied, our simulations show pH and carbonate chemistry are good indicators for leakage of stored CO<sub>2 </sub>into an overlying aquifer because elevated CO<sub>2 </sub>yields a more acid pH than the ambient groundwater. CO<sub>2 </sub>leakage into a dilute groundwater creates a slightly acid plume that can be detected at some distance from the leak source due to groundwater flow and CO<sub>2 </sub>buoyancy. pH breakthrough curves demonstrate that CO<sub>2 </sub>leaks can be easily detected for CO<sub>2 </sub>flux ≥ 10<sup>4 </sup>t/yr within a 15-month time period at a monitoring well screened within a permeable layer 500 m downstream from the vertical gas trace. At lower flux rates, the CO<sub>2 </sub>dissolves in the aqueous phase in the lower most permeable unit and does not reach the monitoring well. Sustained pumping in a developed aquifer mixes the CO<sub>2</sub>-affected water with the ambient water and enhances pH signal for small leaks (10<sup>3 </sup>t/yr) and reduces pH signal for larger leaks (≥ 10<sup>4</sup>t/yr).</p> <p>Conclusion</p> <p>The ability to detect CO<sub>2 </sub>leakage from a storage reservoir to overlying dilute groundwater is dependent on CO<sub>2 </sub>solubility, leak flux, CO<sub>2 </sub>buoyancy, and groundwater flow. Our simulations show that the most likely places to detect CO<sub>2 </sub>are at the base of the confining layer near the water table where CO<sub>2 </sub>gas accumulates and is transported laterally in all directions, and downstream of the vertical gas trace where groundwater flow is great enough to transport dissolved CO<sub>2 </sub>laterally. Our simulations show that CO<sub>2 </sub>may not rise high enough in the aquifer to be detected because aqueous solubility and lateral groundwater transport within the lower aquifer unit exceeds gas pressure build-up and buoyancy needed to drive the CO<sub>2 </sub>gas upwards.</p
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