An improved understanding about CO2 EOR and CO2 storage in liquid-rich shale reservoirs

During the past decade, enhanced oil recovery (EOR) by CO2 in shale oils has received substantial attention. In shale oil reservoirs, CO2 diffusion into the resident oil has been considered as the dominant interaction between the CO2 in fractures and the oil in the matrices. CO2 diffusion will lead to oil swelling and improvement in oil viscosity. However, despite two-way mass transfer during CO2 EOR in conventional oil reservoirs, one-way mass transfer into shale oils saturated with live oils is controlled by an additional transport mechanism, which is the liberation of light oil components in the form of a gaseous new-phase. This in-situ gas formation could generate considerable swelling, which could improve the oil recovery significantly. This mechanism has been largely overlooked in the past. This study is aimed to better understand the role of this evolving gas phase in improving hydrocarbon recovery. Taking account of Bakken shale oil reservoir data, numerical simulations were performed to identify efficiencies of EOR by CO2 at the laboratory and field scales. Equation of state parameters between CO2 and oil components were adjusted to optimize the calculations and a sensitivity analysis was performed to identify the role of gas formation and consequent EOR efficiencies. At the laboratory scale, in-situ gas formation can increase oil recovery by 20% depending on the amount of gas saturation. Also, the CO2 storage capacity of the shale matrix can be enhanced by 25%, due to CO2 trapping in the gas phase. At the field scale, an additional oil recovery of 9.1% could be attained, which is notably higher than previous studies where this gas evolution mechanism was ignored. Furthermore, the results suggest that a six-weeks huff period would be sufficient to achieve substantial EOR if this new mechanism is incorporated. On the other hand, the produced fluid in the early period was primarily composed of CO2, which would make it available for subsequent cycles. The produced gas of the well under CO2 EOR was used in an adjacent well, which resulted in similar additional oil recovery and hence, impurities in CO2 injection stream would not undermine efficiency of this EOR method. The results of this study, therefore, could potentially be used to substantially improve the evaluations of CO2 EOR in liquid-rich shale reservoirs

Carbon sequestration potential of altered mafic reservoirs

Porous basaltic aquifers are currently being considered as a key geologic carbon storage host due to its widespread distribution and high reactivity. The co-injection of CO2 and groundwater into basaltic reservoirs has the potential to mineralize this gas into solid phases within years, thanks to the release of divalent cations. Many natural basalts, however, contain substantial alteration minerals. Here we explore the potential of basalt alteration minerals to provide the Ca to fix injected CO2 within calcite and/or aragonite. Preliminary results suggest that altered basaltic rocks can provide this Ca as efficiently as fresh basalts at 25 and 100 °C. Further experimental work is ongoing to confirm these findings at different temperatures and as a function of injected fluid chemistry

Can Mg isotopes be used to trace cyanobacteria-mediated magnesium carbonate precipitation in alkaline lakes?

The fractionation of Mg isotopes was determined during the cyanobacterial mediated precipitation of hydrous magnesium carbonate precipitation in both natural environments and in the laboratory. Natural samples were obtained from Lake Salda (SE Turkey), one of the few modern environments on the Earth's surface where hydrous Mg-carbonates are the dominant precipitating minerals. This precipitation was associated with cyanobacterial stromatolites which were abundant in this aquatic ecosystem. Mg isotope analyses were performed on samples of incoming streams, groundwaters, lake waters, stromatolites, and hydromagnesite-rich sediments. Laboratory Mg carbonate precipitation experiments were conducted in the presence of purified Synechococcus sp cyanobacteria that were isolated from the lake water and stromatolites. The hydrous magnesium carbonates nesquehonite (MgCO3·3H2O) and dypingite (Mg5(CO3)4(OH)25(H2O)) were precipitated in these batch reactor experiments from aqueous solutions containing either synthetic NaHCO3/MgCl2 mixtures or natural Lake Salda water, in the presence and absence of live photosynthesizing Synechococcus sp. Bulk precipitation rates were not to affected by the presence of bacteria when air was bubbled through the system. In the stirred non-bubbled reactors, conditions similar to natural settings, bacterial photosynthesis provoked nesquehonite precipitation, whilst no precipitation occurred in bacteria-free systems in the absence of air bubbling, despite the fluids achieving a similar or higher degree of supersaturation. The extent of Mg isotope fractionation (?26Mgsolid-solution) between the mineral and solution in the abiotic experiments was found to be identical, within uncertainty, to that measured in cyanobacteria-bearing experiments, and ranges from ?1.4 to ?0.7 ‰. This similarity refutes the use of Mg isotopes to validate microbial mediated precipitation of hydrous Mg carbonate

The surface area and reactivity of granitic soils: I. Dissolution rates of primary minerals as a function of depth and age deduced from field observations

Surface area-normalised dissolution rates of the primary minerals in two distinct granitic soils located in 1) the Dartmoor National Park, England and 2) Glen Dye, Scotland were determined as a function of depth. Each soil was sampled to a depth of ~ 1 m. The maximum soil ages based on 14C analysis of the humin fraction of the soil are 15,600 and 4400 years for the Dartmoor and Glen Dye soil profiles, respectively. The measured BET surface areas of the soil minerals are close to 5 m2/g in the B and C horizons, but decrease to less than 1 m2/g close to the surface. Retrieved geometric surface area normalised mineral dissolution rates are most rapid at the surface and at the bedrock–soil interface; this behaviour is interpreted to stem from a combination of the approach to equilibrium of the soil waters with depth and more rapid dissolution rates of fresh versus weathered surfaces. At the soil surface, the relative mineral dissolution rate order is found to be quartz > feldspar > mica, with quartz geometric surface area dissolution rates as fast as 2.6 to 4.1 × 10− 13 mol/m2/s. As observed in a number of past studies, field based rates obtained in this study are significantly slower than corresponding rates obtained from laboratory studies, suggesting that these latter rates may not accurately describe the reactivity of primary minerals in soils

Evidence for the super Tonks-Girardeau gas

We provide evidence in support of a recent proposal by Astrakharchik at al. for the existence of a super Tonks-Girardeau gas-like state in the attractive interaction regime of quasi-one-dimensional Bose gases. We show that the super Tonks-Giradeau gas-like state corresponds to a highly-excited Bethe state in the integrable interacting Bose gas for which the bosons acquire hard-core behaviour. The gas-like state properties vary smoothly throughout a wide range from strong repulsion to strong attraction. There is an additional stable gas-like phase in this regime in which the bosons form two-body bound states behaving like hard-core bosons.Comment: 10 pages, 1 figure, 2 tables, additional text on the stability of the super T-G gas-like stat

Bethe Ansatz study of one-dimensional Bose and Fermi gases with periodic and hard wall boundary conditions

We extend the exact periodic Bethe Ansatz solution for one-dimensional bosons and fermions with delta-interaction and arbitrary internal degrees of freedom to the case of hard wall boundary conditions. We give an analysis of the ground state properties of fermionic systems with two internal degrees of freedom, including expansions of the ground state energy in the weak and strong coupling limits in the repulsive and attractive regimes.Comment: 27 pages, 6 figures, key reference added, typos correcte

A collective effort to identify and quantify geo-energy risks

The increasing global demand for energy and the imminent need to reduce carbon emissions in our planet has led mankind to find new solutions. Some in the energy industry have taken special interest in geothermal reservoirs, a resource with the potential to provide large amounts of renewable energy. Meanwhile, the storage of carbon dioxide in underground geological formations presents a fantastic opportunity to discard CO2 and mitigate global warming. This study links efforts from academic institutions, industry energy operators, industrial partners and research institutes to answer fundamental scientific questions that can help us understand the subsurface and generate better exploitation practices. We examine the geology of reservoirs used for geothermal energy extraction and carbon dioxide capture. We use a combination of field geology, photogrammetry, mineral analysis and experimental rock mechanics to understand fracture networks and fluid flow paths of two geologically diverse reservoirs in Europe: 1) the Hengill geothermal system in south-west Iceland, and 2) the Carnmenellis granite geothermal system in Cornwall (UK). These results aim to provide experimental data to refine numerical models predicting fluid flow and contribute to the quantification of the associated risks of exploiting the subsurface

Exact results for the thermal and magnetic properties of strong coupling ladder compounds

We investigate the thermal and magnetic properties of the integrable su(4) ladder model by means of the quantum transfer matrix method. The magnetic susceptibility, specific heat, magnetic entropy and high field magnetization are evaluated from the free energy derived via the recently proposed method of high temperature expansion for exactly solved models. We show that the integrable model can be used to describe the physics of the strong coupling ladder compounds. Excellent agreement is seen between the theoretical results and the experimental data for the known ladder compounds (5IAP)$_2$CuBr$_4$$\cdot$2H$_2$O, Cu$_{2}$(C$_5$H$_{12}$N$_2$)$_2$Cl$_4$ etc.Comment: 10 pages, 5 figure