Influence of Rock Mineralogy on Reactive Fracture Evolution in Carbonate-Rich Caprocks
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The natural mode of retention of mercury in flue gas desulfurization gypsum used in wallboard manufacturing has been investigated using a series of phase-targeted reagents. Results indicate that mercury was associated with two distinct phases.
Characterization and geochemical data are presented from a core-flooding experiment on a sample from the Three Fingers evaporite unit forming the lower extent of caprock at the Weyburn-Midale reservoir, Canada. This low-permeability sample was characterized in detail using X-ray computed microtomography before and after exposure to CO 2 -acidified brine, allowing mineral phase and voidspace distributions to be quantified in three dimensions. Solution chemistry indicated that CO 2 -acidified brine preferentially dissolved dolomite until saturation was attained, while anhydrite remained unreactive. Dolomite dissolution contributed to increases in bulk permeability through the formation of a localized channel, guided by microfractures as well as porosity and reactive phase distributions aligned with depositional bedding. An indirect effect of carbonate mineral reactivity with CO 2 -acidified solution is voidspace generation through physical transport of anhydrite freed from the rock matrix following dissolution of dolomite. The development of high permeability fast pathways in this experiment highlights the role of carbonate content and potential fracture orientations in evaporite caprock formations considered for both geologic carbon sequestration and CO 2 -enhanced oil recovery operations.
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We conduct numerical shear experiments on mixtures of quartz and talc gouge using a three-dimensional (3D) distinct element model. A modified slip-weakening constitutive law is applied at contacts. We perform velocity-stepping experiments on both uniform and layered mixtures of quartz and talc analogs. We separately vary the proportion of talc in the uniform mixtures and talc layer thickness in the layered mixtures. Shear displacements are cycled through velocities of 1 and 10 μm/s. We follow the resulting evolution of ensemble shear strength, slip stability, and permeability of the gouge mixture and explore the mesoscopic mechanisms. Simulation results show that talc has a strong weakening effect on shear strength—a thin shear-parallel layer of talc (three particles wide) can induce significant weakening. However, the model offsets laboratory-derived strong weakening effects of talc observed in uniform mixtures, implying the governing mechanisms may be the shear localization effect of talc, which is enhanced by its natural platy shape or preimposed layered structure. Ensemble stability (a – b ) can be enhanced by increasing talc content in uniform talc-quartz mixtures. Reactivation-induced permeability increase is amplified with increased quartz content before the maturation of shear localization. Postmaturation permeability enhances on velocity upsteps and diminishes on velocity downsteps. Talc enhances compaction at velocity downsteps, potentially reducing fault permeability. Evolution trends of stability relating to the composition and structure of the fault gouge are straightforwardly obtained from the 3D simulation. Local friction evolution indicates that talc preferentially organizes and localizes in the shear zone, dominating the shear strength and frictional stability of faults
Microbe-mineral interactions are ubiquitous and can facilitate major biogeochemical reactions that drive dynamic Earth processes such as rock formation. One example is microbially induced calcium carbonate precipitation (MICP) in which microbial activity leads to the formation of calcium carbonate precipitates. A majority of MICP studies have been conducted at the mesoscale but fundamental questions persist regarding the mechanisms of cell encapsulation and mineral polymorphism. Here, we are the first to investigate and characterize precipitates on the microscale formed by MICP starting from single ureolytic E. coli MJK2 cells in 25 µm diameter drops. Mineral precipitation was observed over time and cells surrounded by calcium carbonate precipitates were observed under hydrated conditions. Using Raman microspectroscopy, amorphous calcium carbonate (ACC) was observed first in the drops, followed by vaterite formation. ACC and vaterite remained stable for up to 4 days, possibly due to the presence of organics. The vaterite precipitates exhibited a dense interior structure with a grainy exterior when examined using electron microscopy. Autofluorescence of these precipitates was observed possibly indicating the development of a calcite phase. The developed approach provides an avenue for future investigations surrounding fundamental processes such as precipitate nucleation on bacteria, microbe-mineral interactions, and polymorph transitions.
Presented by NETL at Geological Society of America Annual Scientific, 11/18
Taking advantage of the bent uranyl-peroxide-uranyl interaction found in studtite, 26 nanoscale clusters have been synthesized using uranyl hexagonal bipyramids. Sixteen of these clusters are built from uranyl hexagonal bipyramids only. Eight contain pyrophosphate groups that bridge between uranyl polyhedra, and two contain oxalate groups that adopt a similar structural role. These clusters contain from 20 to 60 uranyl polyhedra and have diameters in the range ~1.5 to 3 nm. All spontaneously self-assemble in aqueous solution under ambient conditions.
If there’s one word that describes Matt Kohn’s career, it’s eclectic. What is possibly most astounding is that Matt’s contributions have not been in a single, narrow field, but in two distinct fields that, at least at first glance, are not even that closely related. While Matt is a metamorphic petrologist par excellence making significant contributions to the fields of geo-thermobarometry, metamorphic phase equilibria, metamorphic fluid flow, monazite geochronology, argon geochronology, and metamorphic P-T-t studies and their tectonic implications, he has also pioneered the use of stable isotopes to unravel vertebrate paleodietary patterns and paleoclimate.
This section is not intended to be comprehensive or detailed, because diffraction is such a vast subject. The principles of diffraction theory, however, are summarized under the assumption that the reader is familiar with basic concepts of the crystalline state. We will briefly review the basics of diffraction techniques, using laboratory and synchrotron X-ray sources and highlight some of their applications in geoscience.
Seismic reflection the primary tool used in petroleum exploration and production, but use in geothermal exploration is less standard, in part due to cost but also due to the challenges in identifying the highly-permeable zones essential for economic hydrothermal systems [e.g. Louie et al., 2011; Majer, 2003]. Newer technology, such as wireless sensors and low-cost high performance computing, has helped reduce the cost and effort needed to conduct 3D surveys. The second difficulty, identifying permeable zones, has been less tractable so far. Here we report on the use of seismic attributes from a 3D seismic survey to identify and map permeable zones in a hydrothermal area.
Pahute Mesa (PM) in southern Nevada was one of the four principal underground nuclear testing areas at the Nevada National Security Site (NNSS), known as the “Nevada Test Site” until 2010 (Figure 1). Eighty-two underground nuclear tests were conducted at PM in northwestern corner of NNSS (USDOE, 2015). The PM area of underground nuclear testing is located near the center of the Pahute Mesa and Oasis Valley (PM-OV) groundwater basin, which discharges to the southwest near Oasis Valley (OV) north of Beatty, Nevada (Fenelon et al. 2016; Jackson et al., 2020). Most of the PM tests were located at depths near or below the regional water table and, therefore, present potential sources of groundwater contamination from release of test-related radionuclides.
Atmospheric supply of iron can modulate ocean biogeochemistry, due to its key role in global nitrogen and carbon cycles. Using a detailed technology-based methodology we revise total and soluble anthropogenic iron emissions and resolve iron into its mineral components, which allows modeling mineral-specific atmospheric reactions. The inclusion of metal smelting as an iron source, increases fine iron aerosol emissions (smaller than 1 µm) compared with most previous inventories. Different assumptions about solubility lead to estimates of 40-450 Gg/year deposition of soluble anthropogenic iron. When combined with dust and wildfires, the global total anthropogenic soluble iron deposition is 1900-2300 Gg/yr, so assumptions in anthropogenic inventories can affect estimates of global soluble iron supply by about 30%. In regions where marine primary productivity is iron-limited, anthropogenic combustion-iron contributes up to half of the atmospheric soluble iron flux to North Pacific Ocean.
Strontium-90 (Sr-90) is a contaminant of concern in groundwater and surface water at both F-Area and H-Area Seepage Basins. This contaminant was disposed of, along with other heavy metals and radionuclides, into a series of unlined seepage basins from 1955 until 1988. The acidity of the wastewater increased Sr-90 mobility from the basin soil through the vadose zone and into the Upper Aquifer Zone (UAZ), creating a groundwater plume that discharges into wetlands areas and a local stream called Fourmile Branch.