Efficient Microwave Approaches for Extracting Water from Hydrated Minerals
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The presence of water ice in permanently shadowed regions on the lunar surface may enable a sustained human presence on the Moon with minimal need for consumables. In order to successfully extract water from lunar regolith, there are a few physical behaviors that should be accounted for when designing systems to handle icy regolith samples. Many of these behaviors have been observed and recorded in the process of testing ISRU technologies.
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Olivine is one of the major minerals in chondritic meteorites and occurs in all chondritic components, including amoeboid olivine aggregates (AOAs), forsterite-bearing Type B (FoB) Ca, Al-rich inclusions (CAIs), chondrules, and matrices. As a result, olivines could preserve chemical and isotopic characteristics of their formation environments. There are significant variations in oxygen isotopic compositions of chondritic olivine. Forsteritic olivine in AOAs and FoB-CAIs has solar-like 16O-rich compositions (D17O ~ -23±2‰); the former condensed from an 16O-rich gas of ~solar composition, whereas the latter crystallized from remelted condensates in an isotopic similar gaseous reservoir. Olivine phenocrysts in chondrules are significantly 16O-depleted compared to CAIs and AOAs: D17O ranges from ~ -7 to +3‰. Only rare relict olivines in chondrules have CAI/AOA-like 16O-rich compositions; these grains most likely represent fragments of CAIs and AOAs incompletely melted during chondrule formation. Olivine in matrices of weakly metamorphosed meteorites is extremely fine-grained (<100 nm) and has predominantly forsteritic composition. In metamorphosed chondrites, matrix olivines are coarse-grained (up to 10 μm) and enriched in FeO. Due to small grain sizes, oxygen isotopic compositions of matrix olivines are poorly known. Mapping of matrices of Vigarano and Kakangari using isotope microscopes (secondary ion mass-spectrometer (SIMS) plus SCAPS detector) revealed the presence of 16O-rich olivine grains. While most matrix olivines in Vigarano have 16O-poor compositions, nearly half of olivines measured in Kakangari matrix are16O-rich.Here, we present for the first time new lithologies largely composed of 16O-and Fe-rich olivine. We attempt to address the question of whether these 16O-richolivine grains were formed by condensation in the solar nebula or by a secondary process during the evolution of the parent body. Mineralogical characteristics of these unusual olivines, as well as in-situ measured oxygen-isotope compositions of different phases are reported in detail.
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In the summer and fall of 2023, the Gulf of Mexico Deepwater Hydrate Coring Expedition (UT-GOM2-2) drilled, cored, made downhole measurements, and analyzed samples from the seafloor to the base of the gas hydrate stability zone in one location (Site H, WR313) in the Terrebonne basin, deepwater Gulf of Mexico. Analyses of data and samples from the expedition will inform biological, geochemical, and geomechanical models to constrain the role of gas hydrates in the carbon cycle and the potential for gas hydrates as an energy resource. Pressure and conventional cores were collected continuously to a depth of 155.1 meters below the seafloor (mbsf). At deeper depths, cores were taken periodically from hydrate-bearing sands and their bounding muds to a total depth of 861.3 mbsf. 162.6 m of conventional core and 54.8 m of pressure core were obtained. Twelve temperature measurements were made between 27.1 and 144.5 mbsf to determine the geothermal gradient. At the seafloor, more than 4 m of sandy silt of unknown origin was encountered. Beneath this sand, to a depth of ~200 mbsf, the section was composed of interbedded mud and biogenic carbonate ooze. The biogenic ooze correlated to low density and high porosity intervals observed in the previously acquired logging while drilling (LWD) data and as measured. Calcareous nannofossil biostratigraphy constrains the entire record to the Pleistocene (< 0.91 million years) with a pronounced increase in sedimentation rate with depth. Beneath 200 mbsf, the section was predominantly composed of mud with two thicker, hydrate-bearing coarse-grained intervals, which are commonly known as the Blue and Orange sands. The dissolved gas concentration was quantified from pressure cores. In the shallow section, dissolved methane concentration increased below the sulfate-methane transition zone (SMTZ) and reaches saturation (the limit of solubility for methane) at 147 mbsf. Gas expansion was very common in conventional and depressurized pressure (conventionalized) cores below the SMTZ. At deeper depths, the methane concentration within muds bounding the Blue and Orange reservoirs was generally found to be less than saturation. The dissolved and hydrate gas composition is consistent with a microbial source, containing greater than 99.99% methane and only trace concentrations of ethane, propane, and butane. The methane to ethane ratio (C 1 /C 2 ) and the methane to ethane plus propane (C 1 /(C 2 +C 3 )) decrease with depth down to at least 678 mbsf, mainly driven by the increase in ethane with depth. It is unclear if this trend continues through the Orange sand interval. The δ 13 C isotopic signature of methane ranges between -69.9 and -78.5 ‰ Vienna Pee Dee Belemnite (VPDB). Pressure core recovery of all sandy intervals was poor. However, pressure core logs of the Orange sand show intervals of low density and high velocity, which are indicative of high hydrate saturation. One core from within the Orange sand was composed of interbedded graded sandy silt and mud. The sandy silts from this core are composed of mainly quartz and feldspar with some lithics. Most of the recovered pressure core samples are maintained at near in-situ pressure and temperature (within the hydrate stability field) at the University of Texas Pressure Core Center awaiting analysis. In the shallow section, samples will be used to determine the flux of organic carbon through the basin system, find the rate at which that carbon was consumed, and understand the microbial population responsible for these processes. In the deeper section, samples from in and around the hydrate reservoirs will be used to determine the petrophysical properties of the reservoir and bounding seals in these systems.