Modeling acid-gas generation from boiling chloride brines

<p>Abstract</p> <p>Background</p> <p>This study investigates the generation of HCl and other acid gases from boiling calcium chloride dominated waters at atmospheric pressure, primarily using numerical modeling. The main focus of this investigation relates to the long-term geologic disposal of nuclear waste at Yucca Mountain, Nevada, where pore waters around waste-emplacement tunnels are expected to undergo boiling and evaporative concentration as a result of the heat released by spent nuclear fuel. Processes that are modeled include boiling of highly concentrated solutions, gas transport, and gas condensation accompanied by the dissociation of acid gases, causing low-pH condensate.</p> <p>Results</p> <p>Simple calculations are first carried out to evaluate condensate pH as a function of HCl gas fugacity and condensed water fraction for a vapor equilibrated with saturated calcium chloride brine at 50-150°C and 1 bar. The distillation of a calcium-chloride-dominated brine is then simulated with a reactive transport model using a brine composition representative of partially evaporated calcium-rich pore waters at Yucca Mountain. Results show a significant increase in boiling temperature from evaporative concentration, as well as low pH in condensates, particularly for dynamic systems where partial condensation takes place, which result in enrichment of HCl in condensates. These results are in qualitative agreement with experimental data from other studies.</p> <p>Conclusion</p> <p>The combination of reactive transport with multicomponent brine chemistry to study evaporation, boiling, and the potential for acid gas generation at the proposed Yucca Mountain repository is seen as an improvement relative to previously applied simpler batch evaporation models. This approach allows the evaluation of thermal, hydrological, and chemical (THC) processes in a coupled manner, and modeling of settings much more relevant to actual field conditions than the distillation experiment considered. The actual and modeled distillation experiments do not represent expected conditions in an emplacement drift, but nevertheless illustrate the potential for acid-gas generation at moderate temperatures (<150°C).</p

Geochemical detection of carbon dioxide in dilute aquifers

<p>Abstract</p> <p>Background</p> <p>Carbon storage in deep saline reservoirs has the potential to lower the amount of CO₂emitted 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 CO₂gas leak into dilute groundwater are important measures for the potential release of CO₂to 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 CO₂storage reservoir. Specifically, we address the relationships between CO₂flux, groundwater flow, detection time and distance. The CO₂flux ranges from 10³to 2 × 10⁶t/yr (0.63 to 1250 t/m²/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 CO₂into an overlying aquifer because elevated CO₂yields a more acid pH than the ambient groundwater. CO₂leakage 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 CO₂buoyancy. pH breakthrough curves demonstrate that CO₂leaks can be easily detected for CO₂flux ≥ 10⁴t/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 CO₂dissolves 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 CO₂-affected water with the ambient water and enhances pH signal for small leaks (10³t/yr) and reduces pH signal for larger leaks (≥ 10⁴t/yr).</p> <p>Conclusion</p> <p>The ability to detect CO₂leakage from a storage reservoir to overlying dilute groundwater is dependent on CO₂solubility, leak flux, CO₂buoyancy, and groundwater flow. Our simulations show that the most likely places to detect CO₂are at the base of the confining layer near the water table where CO₂gas accumulates and is transported laterally in all directions, and downstream of the vertical gas trace where groundwater flow is great enough to transport dissolved CO₂laterally. Our simulations show that CO₂may 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 CO₂gas upwards.</p

Inter-seasonal compressed air energy storage using saline aquifers

Meeting inter-seasonal fluctuations in electricity production or demand in a system dominated by renewable energy requires the cheap, reliable and accessible storage of energy on a scale that is currently challenging to achieve. Commercially mature compressed-air energy storage could be applied to porous rocks in sedimentary basins worldwide, where legacy data from hydrocarbon exploration are available, and if geographically close to renewable energy sources. Here we present a modelling approach to predict the potential for compressed-air energy storage in porous rocks. By combining this with an extensive geological database, we provide a regional assessment of this potential for the United Kingdom. We find the potential storage capacity is equivalent to approximately 160% of the United Kingdom’s electricity consumption for January and February 2017 (77–96 TWh), with a roundtrip energy efficiency of 54–59%. This UK storage potential is achievable at costs in the range US$0.42–4.71 kWh−1