Comparison of lattice Boltzmann method and pore-network modeling of CO2 and brine flow in Mt Simon Sandstone
Presented by NETL at 8th International Conference on Porous Media; InterPore2016; 5/2016
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Presented by NETL at 8th International Conference on Porous Media; InterPore2016; 5/2016
Presented by NETL at 2016 Fall AGU Meeting; 12/16
In order to utilize as much of the pore space for CO 2 storage in high permeability thick saline aquifers, it is vital to investigate the interactions of injected CO 2 with formation brine and rock. In order to quantify the displacement process, we investigate the dynamic storage efficiency factor (DSEF) for saline aquifers where pressure increase is minimal during the injection phase. Dimensionless numbers are derived from basic governing equations, constitutive equations, initial and boundary conditions using the inspection analysis. Then using the Hammersley sequence sampling, 178 numerical experiments are designed, and a compositional reservoir simulator is used to perform these simulations. In the next step, response surface regression analysis is used to establish a relationship between DSEF obtained from the numerical simulations and the corresponding dimensionless numbers. The simulation results show that for the studied conditions the underground dynamics is mostly influenced by the gravity number, followed by effective aspect ratio and dip numbers. The results from the response surface regression analysis are used to develop a correlation, which can be used to estimate the dynamic CO 2 storage capacity of relevant zones. This study provides quantitative measures for the different competing mechanisms involved in underground displacement of fluids in CO 2 geological storage, which can serve as a useful tool during planning phase of storage projects.
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Low-salinity waterflooding has emerged as an innovative technique to improve oil recovery. Extensive research has been devoted to providing a better understanding of the mechanisms involved and to optimize its performance. Among those mechanisms, multi-component ion exchange mechanism explains the coordination of surface complexes in a way that highlights the essence of low-salinity waterflooding. However, the impact of temperature on low-salinity waterflooding is still poorly understood. We used surface complexation modeling to study both the oil/brine and mineral/brine interfaces up to a temperature of 150 °C. Given the heterogeneity of the oil interface, we studied three oil interfaces with varying total base number to total acid number ratios. It was determined that temperature is a critical factor in estimating the performance of low-salinity waterflooding. While temperature reduces the pH range at which low-salinity waterflooding yields positive effect for basic oil, it shifts the pH window at which low-salinity waterflooding has potentially negative results to lower pH values for neutral oil. In addition, the temperature magnifies the ability of low-salinity waterflooding to enhance surface potential. Furthermore, our results support the need for conducting experimental work at the relevant reservoir temperature to evaluate the performance of low-salinity waterflooding.
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Deep subsurface storage and sequestration of CO2 has been identified as a potential mitigation technique for rising atmospheric CO2 concentrations. Sequestered CO2 represents a potential risk to overlying aquifers if the CO2 leaks from the deep storage reservoir. Experimental and modeling work is required to evaluate potential risks to groundwater quality and develop a systematic understanding of how CO2 leakage may cause important changes in aquifer chemistry and mineralogy by promoting dissolution/precipitation, adsorption/desorption, and redox reactions. Sediments from the High Plains aquifer in Kansas, United States, were used in this investigation, which is part of the National Risk Assessment Partnership Program sponsored by the US Department of Energy. This aquifer was selected to be representative of consolidated sand and gravel/sandstone aquifers overlying potential CO2 sequestration repositories within the continental US. In this paper, we present results from batch experiments conducted at room temperature and atmospheric pressure with four High Plains aquifer sediments. Batch experiments simulate sudden, fast, and short-lived releases of the CO2 gas as would occur in the case of well failure during injection. Time-dependent release of major, minor, and trace elements were determined by analyzing the contacting solutions. Characterization studies demonstrated that the High Plains aquifer sediments were abundant in quartz and feldspars, and contained about 15 to 20 wt% montmorillonite and up to 5 wt% micas. Some of the High Plains aquifer sediments contained no calcite, while others had up to about 7 wt% calcite. The strong acid extraction tests confirmed that in addition to the usual elements present in most soils, rocks, and sediments, the High Plains aquifer sediments had appreciable amounts of As, Cd, Pb, Cu, and occasionally Zn, which potentially may be mobilized from the solid to the aqueous phase during or after exposure to CO2. However, the results from the batch experiments showed that the High Plains sediments mobilized only low concentrations of trace elements (potential contaminants), which were detected occasionally in the aqueous phase during these experiments. Importantly, these occurrences were more frequent in the calcite-free sediment. Results from these investigations provide useful information to support site selection, risk assessment, and public education efforts associated with geological CO2 storage and sequestration.
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