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At least 955 records · Page 53

Optimized, Budget-constrained Monitoring Well Placement Using DREAM

Defining the ideal suite of monitoring technologies to be deployed at a carbon capture and storage (CCS) site presents a challenge to project developers, financers, insurers, regulators and other stakeholders. The monitoring, verification, and accounting (MVA) toolkit offers a suite of technologies to monitor an extensive range of parameters across a wide span of spatial and temporal resolutions, each with their own degree of sensitivity to changes in the parameter being monitored. Understanding how best to optimize MVA budgets to minimize the time to leak detection could help to address issues around project risks, and in turn help support broad CCS deployment. This paper presents a case study demonstrating an application of the Designs for Risk Evaluation and Management (DREAM) tool using an ensemble of CO 2 leakage scenarios taken from a previous study on leakage impacts to groundwater. Impacts were assessed and monitored as a function of pH, total dissolved solids (TDS), and trace metal concentrations of arsenic (As), cadmium (Cd), chromium (Cr), and lead (Pb). Using output from the previous study, DREAM was used to optimize monitoring system designs based on variable sampling locations and parameters. The algorithm requires the user to define a finite budget to limit the number of monitoring wells and technologies deployed, and then iterates well placement and sensor type and location until it converges on the configuration with the lowest time to first detection of the leak averaged across all scenarios. To facilitate an understanding of the optimal number of sampling wells, DREAM was used to assess the marginal utility of additional sampling locations. Based on assumptions about monitoring costs and replacement costs of degraded water, the incremental cost of each additional sampling well can be compared against its marginal value in terms of avoided aquifer degradation. Applying this method, DREAM identified the most cost-effective ensemble with 14 monitoring locations. Here, while this preliminary study applied relatively simplistic cost and technology assumptions, it provides an exciting proof-of-concept for the application of DREAM to questions of cost-optimized MVA system design that are informed not only by site-specific costs and technology options, but also by reservoir simulation results developed during site characterization and operation.

47 OTHER INSTRUMENTATION↗

Efficient relaxations for joint chance constrained AC optimal power flow

Evolving power systems with increasing levels of stochasticity call for a need to solve optimal power flow problems with large quantities of random variables. Weather forecasts, electricity prices, and shifting load patterns introduce higher levels of uncertainty and can yield optimization problems that are difficult to solve in an efficient manner. Solution methods for single chance constraints in optimal power flow problems have been considered in the literature, ensuring single constraints are satisfied with a prescribed probability; however, joint chance constraints, ensuring multiple constraints are simultaneously satisfied, have predominantly been solved via scenario-based approaches or by utilizing Boole's inequality as an upper bound. In this paper, joint chance constraints are used to solve an AC optimal power flow problem while preventing overvoltages in distribution grids under high penetrations of photovoltaic systems. A tighter version of Boole's inequality is derived and used to provide a new upper bound on the joint chance constraint, and simulation results are shown demonstrating the benefit of the proposed upper bound. The new framework allows for a less conservative and more computationally efficient solution to considering joint chance constraints, specifically regarding preventing overvoltages.

24 POWER TRANSMISSION AND DISTRIBUTION↗

Measurements of 14 C in ancient ice from Taylor Glacier, Antarctica constrain in situ cosmogenic 14 CH 4 and 14 CO production rates

Carbon-14 ( 14 C) is incorporated into glacial ice by trapping of atmospheric gases as well as direct near-surface in situ cosmogenic production. 14 C of trapped methane ( 14 CH 4 ) is a powerful tracer for past CH 4 emissions from “old” carbon sources such as permafrost and marine CH 4 clathrates. 14 C in trapped carbon dioxide ( 14 CO 2 ) can be used for absolute dating of ice cores. In situ produced cosmogenic 14 C in carbon monoxide ( 14 CO) can potentially be used to reconstruct the past cosmic ray flux and past solar activity. Unfortunately, the trapped atmospheric and in situ cosmogenic components of 14 C in glacial ice are difficult to disentangle and a thorough understanding of the in situ cosmogenic component is needed in order to extract useful information from ice core 14 C. Here, we analyzed very large (≈1000 kg) ice samples in the 2.26–19.53 m depth range from the ablation zone of Taylor Glacier, Antarctica, to study in situ cosmogenic production of 14 CH 4 and 14 CO. All sampled ice is >50 ka in age, allowing for the assumption that most of the measured 14 C originates from recent in situ cosmogenic production as ancient ice is brought to the surface via ablation. Our results place the first constraints on cosmogenic 14 CH 4 production rates and improve on prior estimates of 14 CO production rates in ice. We find a constant 14 CH 4 / 14 CO production ratio (0.0076 ± 0.0003) for samples deeper than 3 m, which allows the use of 14 CO for correcting the 14 CH 4 signals for the in situ cosmogenic component. Our results also provide the first unambiguous confirmation of 14 C production by fast muons in a natural setting (ice or rock) and suggest that the 14 C production rates in ice commonly used in the literature may be too high.

58 GEOSCIENCES↗

Constraining the behavior of gallium isotopes during evaporation at extreme temperatures

Renewed interest in gallium isotope systematics has stemmed from the fact that Ga is moderately volatile and is hypothesized to undergo kinetic fractionation during evaporation. In this work, we present the first Ga isotope data from terrestrial volatile depleted samples including a suite of experimentally heated rhyolitic soils, fallout melt glass, and splash-form tektites from the Australasian strewn field (hereafter termed australite tektites). The Ga in these samples is isotopically heavy compared to Ga in terrestrial basalts and estimates for the composition of the bulk silicate Earth (BSE). For each sample suite the isotopic fractionation of Ga scales with the degree of Ga depletion, consistent with isotopic fractionation caused by evaporation.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Mineralogical, magnetic and geochemical data constrain the pathways and extent of weathering of mineralized sedimentary rocks

The oxidative weathering of sulfidic rock can profoundly impact watersheds through the resulting export of acidity and metals. Weathering leaves a record of mineral transformation, particularly involving minor redox-sensitive phases, that can inform the development of conceptual and quantitative models. In sulfidic sedimentary rocks, however, variations in depositional history, diagenesis and mineralization can change or overprint the distributions of these trace minerals, complicating the interpretation of weathering signatures. Here we show that a combination of bulk mineralogical and geochemical techniques, micrometer-resolution X-ray fluorescence microprobe analysis and rock magnetic measurements, applied to drill core samples and single weathered fractures, can provide data that enable the development of a geochemically consistent weathering model. This work focused on one watershed in the Upper Colorado River Basin sitting within the Mesaverde Formation, a sedimentary sandstone bedrock with disseminated sulfide minerals, including pyrite and sphalerite, that were introduced during diagenesis and subsequent magmatic-hydrothermal mineralization. Combined analytical methods revealed the pathways of iron (Fe), carbonate and silicate mineral weathering and showed how pH controls element retention or release from the actively weathering fractured sandstone. Drill core logging, whole rock X-ray diffraction, and geochemical measurements document the progression from unweathered rock at depth to weathered rock at the surface. X-ray microprobe analyses of a 1-cm size weathering profile along a fracture surface are consistent with the mobilization of Fe(II) and Fe(III) into acidic pore water from the dissolution of primary pyrite, Fe-sphalerite, chlorite, and minor siderite and pyrrhotite. These reactions are followed by the precipitation of secondary minerals such as of goethite and jarosite, a Fe-(oxyhydr)oxide and hydrous Fe(III) sulfate, respectively. Microscale analyses also helped explain the weathering reactions responsible for the mineralogical transformations observed in the top and most weathered section of the drill core. For example, dissolution of feldspar and chlorite neutralizes the acidity generated by Fe and sulfide mineral oxidation, oversaturating the solution in both Fe-oxides. The combination of X-ray spectromicroscopy and magnetic measurements show that the Fe(III) product is goethite, mainly present either as a coating on fracture surfaces in the actively weathering region of the core or more homogeneously contained within the unconsolidated regolith at the top of the core. Low-temperature magnetic data reveal the presence of ferromagnetic Fe-sulfide pyrrhotite that, although it occurs at trace concentrations, could provide a qualitative proxy for unweathered sulfide minerals because the loss of pyrrhotite is associated with the onset of oxidative weathering. Pyrrhotite loss and goethite formation are detectable through room-temperature magnetic coercivity changes, suggesting that rock magnetic measurements can determine weathering intensity in rock samples at many scales. In conclusion, this work contributes evidence that the weathering of sulfidic sedimentary rocks follows a geochemical pattern in which the abundance of sulfide minerals controls the generation of acidity and dissolved elements, and the pH-dependent mobility of these elements controls their export to the ground- and surface-water.

58 GEOSCIENCES↗

Constraining the magnitude of the carbon isotope excursion during the Paleocene-Eocene thermal maximum using larger benthic foraminifera

The Paleocene-Eocene thermal maximum (PETM) was an extraordinary pulse of global warming approximately 56 Ma. This warmingevent is associated with an addition of large amounts of 13C-depleted carbon into the atmosphere-ocean system, but the magnitude of the negative carbon isotope excursion (CIE)signaling the PETMand often used to estimate mass of the released carbonis still debated. Here we gauge the CIE magnitude usingsecondary ion mass spectrometry (SIMS) to perform in situ δ 13 C measurements within individual larger benthic foraminifera preserved in a tropical shallow marine limestone section in south Tibet. This SIMS-based δ 13 C record yields a negative CIE (Δ~7‰) comparable in magnitude to that registered by terrestrial records but larger than the ~4‰CIE returned by surface-dwelling planktonic foraminiferain deep-sea records. We therefore posit that the CIE magnitude was~7‰ in the surface ocean, and that theprevious~4‰ estimates for the CIE areattenuated by incomplete preservation and diagenetic overprinting. The large CIE magnitude in the surface ocean (~7‰) and the evidently smaller CIE magnitude registeredby deep-sea benthic foraminifera(~2-3.5‰) arelikely a function of rateand duration of carbon release as well as ocean stratification during the PETM.

58 GEOSCIENCES↗