Post-spreading behavior of impacting fuel drops on stainless steel surface
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Plastic-to-fuel (PTF) technology uses pyrolysis to convert plastic waste—especially non-recycled plastics (NRP)—into ultra-low sulfur diesel (ULSD) fuel. To assess the potential energy and environmental benefits associated with PTF technology, we calculated the energy, water consumption, and greenhouse gas emissions of NRP-derived ULSD and compared the results to those metrics for conventional ULSD fuel. For these analyses, we used the Greenhouse gases, Regulated Emissions and Energy use in Transportation (GREET®) model. Five companies provided pyrolysis process product yields and material and energy consumption data. Co-products of the process included char and fuel gas. Char can be landfilled, which, per the company responses, is the most common practice for this co-product, or it may be sold as an energy product. Fuel gas can be combusted to internally generate process heat and electricity. Sensitivity analyses investigated the influence of co-product handling methodology, product yield, electric grid composition, and assumed efficiency of char combustion technology on life-cycle greenhouse gas emissions. The sensitivity analysis indicates that the GHG emissions would likely be reduced up to 14% when it is compared to conventional ULSD, depending on the co-product treatment method used. NRP-derived ULSD fuel could therefore be considered at a minimum carbon neutral with the potential to offer a modest GHG reduction. Moreover, this waste-derived fuel had 58% lower water consumption and up to 96% lower fossil fuel consumption than conventional ULSD fuel in the base case. In addition to the comparison of PTF fuels with conventional transportation fuels, we also compare the results with alternative scenarios for managing NRP including power generation and landfilling in the United States.
A carbon dioxide (CO 2 ) water-alternating-gas (WAG) pilot was conducted to gain insights into tertiary oil recovery potential via CO 2 flood in the West Ranch Field as part of the Petra Nova project, the world's largest postcombustion CO 2 capture and utilization initiative. With a fluvial formation geology, this is a challenging and novel application of CO 2 enhanced oil recovery. The aim of this study is two-fold. First, to build a predictive dynamic model that incorporates the data acquired during the pilot operation. Second, to utilize this model to provide guidance for optimal design for a field-wide CO 2 EOR operation. Our study began with an initialization of the pilot sector model extracted from a calibrated full-field model. The pilot model calibration follows a two-step hierarchical workflow. First, we performed a large-scale update of the permeability distribution by integrating available bottomhole pressure and multiphase production data. Next, local permeability field is fine-tuned using a streamline-based method to match CO 2 breakthrough times at the producers. The predictive capability of the calibrated model was verified through two blind validation tests: (1) the model showed good agreement with saturation logs acquired at two observation wells; and (2) the model reproduced the CO 2 recovery as a fraction of the injected CO 2 . Sensitivity studies were conducted using the calibrated pilot model to evaluate the effects of various operational parameters. Finally, we performed a Design of Experiment based multi-objective optimization of the CO 2 WAG processes using the influential operational parameters identified from the sensitivity analysis.
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Radioactivity levels for conventional thermal diffusivity test specimens are often prohibitively high for examination with candidate metallic materials, such as tungsten and reduced activation steels for fusion energy. Therefore, in the ongoing Japan–US PHENIX project, irradiation in the high flux isotope reactor (HFIR) was performed with the miniature specimen form of diameter (D) 3 mm × thickness (T) 1/2 mm small disk for thermal diffusivity measurement. In this study, the thermal diffusivity measurement of this miniature specimen is validated using a Netzsch LFA-467 ‘Hyper Flash’ thermal analyzer and ‘graphene nanoplatelets containing agent’. Finally, with careful surface treatment and data analysis, the miniature specimens showed almost the same value as the diameter 10 mm standard specimens.
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The provenance of GEMS (glass with embedded metal and sulfides) in cometary type interplanetary dust particles is investigated using analytical scanning transmission electron microscopy and secondary ion mass spectrometry. We review the current state of knowledge and closely examine the densities, elemental compositions and distributions, iron oxidation states, and isotopic compositions of a subset of GEMS in chondritic porous interplanetary dust. We find that GEMS are underdense with estimated densities that are 35–65% of compositionally equivalent crystalline aggregates. GEMS low densities result in a lower contribution to the bulk compositions of IDPs than has been assumed based on their volume fraction. We also find that element/Si ratios, assumed to be primary (indigenous), are instead perturbed by contamination and secondary alteration, including pulse heating during atmospheric entry. Fe in pyrrhotite inclusions was oxidized and Mg, S, Ca, and Fe were depleted relative to lithophile Al and Si, resulting in reduction in element/Si ratios. Because they trap outgassing elements, Fe-rich oxide rims that formed on the surface of GEMS are serendipitous “witness plates” to the changes in composition that accompany atmospheric entry. As a result of alteration, GEMS elemental compositions cannot reliably inform about their provenance. Except for highly anomalous oxygen isotope ratios measured in some large GEMS grains that indicate a contribution from circumstellar dust, oxygen isotope compositions are generally poor indicators of provenance. Prior work indicates that most GEMS fall close to the terrestrial oxygen isotope composition, which, however, does not exclude a presolar interstellar origin. Nitrogen isotopic compositions are more diagnostic. Elevated 15 N/ 14 N ratios indicate that GEMS accreted in conjunction with formation of organic matter by ion–molecule reactions in a cold (<50 K) presolar environment like the extreme outer nebula or interstellar medium. Considering all observations, we conclude that GEMS are most likely processed interstellar silicates.
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The purpose of this study is to quantify geochemical reactions of CO 2 and brine with subsurface samples taken from the Mt. Simon sandstone and identify any potential alterations of the geomechanical rock properties that could lead to changes observable in seismic monitoring or result in changes of micro seismicity such as those observed at the Illinois Basin-Decatur Project (IBDP) site. Two Mt. Simon sandstone samples from 6919.3 feet (2109.0 m) and 6926.1 feet (2111.1 m) depth were exposed to supercritical CO 2 (scCO 2 ) dissolved in brine at in-situ reservoir conditions for one month. Geochemical, spectral, scanning electron microscopy, and petrophysical methods were used to analyze the samples before and after the one-month exposure. Significant changes were observed. Multiple geomechanical properties were chosen to form the framework against which to interrogate the petrophysical data: Young’s modulus (E), Poisson’s ratio (ν), lambda·rho (λρ), and mu·rho (μρ). In this study we conclude that framework composition, porosity, heterogeneities, effective pressure, and reactive geochemistry are first order controls on trends in the E-μ and λρ-μρ cross plot spaces. Changes in porosity, permeability, dynamic moduli, and brittleness with exposure to these fluids were observed. No change in ultrasonic P-wave attenuation (Q P ) was observed. Geochemical alteration causes a distinct shift in λρ-μρ in both samples as well as changes in E, ν, and P and S wave seismic velocity values. Furthermore, these observations could provide insight into subsurface monitoring using seismic methods including amplitude variation with offset (AVO) classification.
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