11 research outputs found

    Transport in concrete with new CO<sub>2</sub> reduced cements - Reactive Transport Model for Durability Estimations

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    Changes in Specific Surface as observed by NMR, caused by saturation of Chalk with porewater bearing divalent Ions

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    Nuclear Magnetic Resonance (NMR) spectrometry has proved to be a good technique for determining the petrophysical properties of reservoir rocks; such as porosity and pore size distribution. We investigated how pore water rich in divalent ions affect the NMR signal from chalk with two different depositional textures. We compared two cases. The first experiments on outcrop chalk with high salinity brines showed that saturation with divalent ions (Mg2+, Ca2+ and SO4 2-) cause major shifts in the T2 distribution curve, probably due to precipitation in the pore space. In a second set of experiments, fluid samples where precipitation takes place were found to show shifts in the T2 relaxation curve due to the creation of crystals. We were able to identify how differences in the rock texture and precipitants within the pore space may affect the transverse relaxation time by altering the surface-to-volume ratio of the pore space. The results of this work could benefit the ongoing study on the optimization of the water composition for Enhanced Oil Recovery (EOR) methods and shed light on how it can affect the mechanical and physical properties of the rock

    Inverse analyses of effective diffusion parameters relevant for a two-phase moisture model of cementitious materials

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    Here we present an inverse analyses approach to determining the two-phase moisture transport properties relevant to concrete durability modeling. The purposed moisture transport model was based on a continuum approach with two truly separate equations for the liquid and gas phase being connected by the sorption kinetics. The moisture properties of ten binder-systems containing fly ash, calcined clay, burnt shale and gray micro-filler, were investigated experimentally. The experiments used were, (i) sorption test (moisture fixation), (ii) cup test in two different relative humidity intervals, (iii) drying test, and, (iv) capillary suction test. Mass change over time, as obtained from the drying test, the two different cup test intervals and the capillary suction test, was used to obtain the effective diffusion parameters using the proposed inverse analyses approach. The moisture properties obtained with the proposed inverse analyses method provide a good description of the test period for the ten different binder-systems

    Co-Optimization of CO2 Storage and Enhanced Gas Recovery Using Carbonated Water and Supercritical CO2

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    CO2-based enhanced gas recovery (EGR) is an appealing method with the dual benefit of improving recovery from mature gas reservoirs and storing CO2 in the subsurface, thereby reducing net emissions. However, CO2 injection for EGR has the drawback of excessive mixing with the methane gas, therefore, reducing the quality of gas produced and leading to an early breakthrough of CO2. Although this issue has been identified as a major obstacle in CO2-based EGR, few strategies have been suggested to mitigate this problem. We propose a novel hybrid EGR method that involves the injection of a slug of carbonated water before beginning CO2 injection. While still ensuring CO2 storage, carbonated water hinders CO2-methane mixing and reduces CO2 mobility, therefore delaying breakthrough. We use reservoir simulation to assess the feasibility and benefit of the proposed method. Through a structured design of experiments (DoE) framework, we perform sensitivity analysis, uncertainty assessment, and optimization to identify the ideal operation and transition conditions. Results show that the proposed method only requires a small amount of carbonated water injected up to 3% pore volumes. This EGR scheme is mainly influenced by the heterogeneity of the reservoir, slug volume injected, and production rates. Through Monte Carlo simulations, we demonstrate that high recovery factors and storage ratios can be achieved while keeping recycled CO2 ratios low

    A Methodology for Optimizing the Calibration and Validation of Reactive Transport Models for Cement-Based Materials

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    Reactive transport models are useful tools in the development of cement-based materials. The output of cement-related reactive transport models is primarily regarded as qualitative and not quantitative, mainly due to limited or missing experimental validation. This paper presents an approach to optimize the calibration process of reactive transport models for cement-based materials, using the results of several short-term experiments. A quantitative comparison of changes in the hydrate phases (measured using TGA and XRD) and exposure solution (measured using ICP-OES) was used to (1) establish a representative chemical model, limiting the number of hydrate phases and dissolved species, and (2) calibrate the transport processes by only modeling the initial tortuosity. A case study comprising the early age carbonation of cement is presented to demonstrate the approach. The results demonstrate that the inclusion of a microstructure model in our framework minimizes the impact of the initial tortuosity factor as a fitting parameter for the transport processes. The proposed approach increases the accuracy of reactive transport models and, thus, allowing for more realistic modeling of long-term exposure

    Assessing the potential of solubility trapping in unconfined aquifers for subsurface carbon storage

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    Abstract Carbon capture and storage projects need to be greatly accelerated to attenuate the rate and degree of global warming. Due to the large volume of carbon that will need to be stored, it is likely that the bulk of this storage will be in the subsurface via geologic storage. To be effective, subsurface carbon storage needs to limit the potential for CO2 leakage from the reservoir to a minimum. Water-dissolved CO2 injection can aid in this goal. Water-dissolved CO2 tends to be denser than CO2-free water, and its injection leads immediate solubility storage in the subsurface. To assess the feasibility and limits of water-dissolved CO2 injection coupled to subsurface solubility storage, a suite of geochemical modeling calculations based on the TOUGHREACT computer code were performed. The modelled system used in the calculations assumed the injection of 100,000 metric tons of water-dissolved CO2 annually for 100 years into a hydrostatically pressured unreactive porous rock, located at 800 to 2000 m below the surface without the presence of a caprock. This system is representative of an unconfined sedimentary aquifer. Most calculated scenarios suggest that the injection of CO2 charged water leads to the secure storage of injected CO2 so long as the water to CO2 ratio is no less than ~ 24 to 1. The identified exception is when the salinity of the original formation water substantially exceeds the salinity of the CO2-charged injection water. The results of this study indicate that unconfined aquifers, a generally overlooked potential carbon storage host, could provide for the subsurface storage of substantial quantities of CO2
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