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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS1994

Degassing history and evolution of volcanic activity of terrestrial planets based on radiogenic noble gas degassing models

Current abundances of radiogenic noble gases (4-He, 40-Ar, 129-Xe) in the planetary atmospheres provide valuable information on planetary evolution through their degassing histories. Of these, 40-Ar (from 40-K with half life 1.25 Ga) can be used to envisage long-term degassing from their interior. Present amounts of 36 and 40-Ar should have information on timing and degree of degassing from the interior. On the other hand, 129-Xe (from 129-I with half life 17 Ma) is used in discussing early planetary degassing. Because life time of helium in the atmosphere is short, atmospheric 4-He (from 235-U, 238-U, 232-Th) data might be used only for current degassing. The relative abundance of 40-Ar in the Cytherean atmosphere is 0.26 of that in the Earth's atmosphere. We have executed numerical calculation of a 40-Ar degassing model along with mantle evolution and melt migration. Our result shows that the average magma production rate on Venus is about 5 (km(exp 3)/yr). Duration of plate motion on Venus, if existed, would be less than several hundred million years.

Sasaki, S.↗
NASA NTRS1994

Rates of Earth degassing

The degassing of the Earth during accretion is constrained by Pu-U-I-Xe systematics. Degassing was much more efficient during the first 100-200 Ma than subsequently, and it was more complete for Xe than for the lighter gases. More than 90 percent of the degassed Xe escaped from the atmosphere during this period. The combination of fractional degassing of melts and rare gas escape from the atmosphere is able to explain the deficit of terrestrial Xe as a simple consequence of this early degassing history. By the time Xe was quantitatively retained in the atmosphere, the abundances of Kr and the lighter gases in the Earth's interior were similar to or higher than the present-day atmospheric abundances. Subsequent transfer of these lighter rare gases into the atmosphere requires a high rate of post-accretion degassing and melt production. Considerations of Pu-U-Xe systematics suggest that relatively rapid post-accretion degassing was continued to ca. 4.1-4.2 Ga. The present-day degassing history of the Earth is investigated through consideration of rare gas isotope abundances. Although the Earth is a highly degassed body, depleted in rare gases by many orders of magnitude relative to their solar abundances, it is at the present-day losing primordial rare gases which were trapped at the time of accretion.

Onions, R. K.↗
DOE OSTI2026

Degassing fluxes in a temperate hydropower reservoir predictable by deep‐water dissolved oxygen but highly sensitive to discharge variability

Hydropower reservoirs contribute to methane (CH 4 ) and carbon dioxide (CO 2 ) emissions, like all aquatic ecosystems. Unique to hydropower reservoirs are degassing emissions that occur when deep-water intakes move water with high CH 4 and CO 2 concentrations through turbines, leading to the release of these gases. However, few studies from hydropower reservoirs have measured seasonal variability and drivers of degassing fluxes, especially in temperate systems. We measured monthly degassing emissions in temperate Douglas Reservoir (Tennessee, USA) from 2023 to 2024. We found that degassing fluxes were highest in the summertime, and deep-water CH 4 and CO 2 concentrations were predictable by deep-water dissolved oxygen (DO) concentrations. Degassing emissions accounted for 37–62% of annually estimated CH 4 emissions, outweighing ebullitive emissions during summer months. We highlight the value of using DO data to estimate deep-water CH 4 and CO 2 concentrations and degassing fluxes at higher temporal resolution to improve annualization and extrapolation of reservoir degassing emissions at broader scales.

Pilla, Rachel M. [Oak Ridge National Laboratory (O↗
NASA NTRS1994

Impact degassing of water and noble gases from silicates

Previous shock experiments by Ahrens and his colleagues show that degassing of H2O and CO2 occurs at 8-65GPa from hydrous minerals such as serpentine. In early solar system, the impact degassing would have played an important part in the formation of primary-atmospheres of the terrestrial planets. However, degassing conditions of noble gases are not well-known because there are few experiments for them. We conducted some shock recovery experiments to investigate the degassing condition and to understand the degassing mechanisms of water and noble gases. We used natural richterites (Ri), amphibolites (Am), serpentines (Sep) and orthoclases (or) as target samples. These, except Sep, contain radiogenic noble gases such as (40)Ar. The samples were put in stainless steel containers, and were show by a rail gun at ISAS or single-stage powder guns at Nagoya or Tohoku University, Japan. We used two kinds of containers: 'open' type containers having a ventilating path for released volatiles for most of samples and 'closed' type ones for some samples for comparison. On Ri and Sep, we made shock experiments for pre-heated (at 400-500 C) and unheated targets, and for powdered and uncrushed samples. Water and noble gases were analyzed both for the recovered shocked samples and the unshocked original samples, and the fractions of the degassed volatiles were calculated by comparing them. Water content in the sample was analyzed by thermo-gravimetry. Noble gases were extracted by heating the samples under high vacuum and analyzed with a sector-type mass spectrometer.

Azuma, S.↗
NASA NTRS1996

Sulfur, Chlorine, and Flourine Degassing and Atmospheric Loading by the 1783 - 1784 AD Laki (Skaftar Fires) Eruption in Iceland

The 1783-1784 Laki tholeiitic basalt fissure eruption in Iceland was one of the greatest atmospheric pollution events of the past 250 years, with widespread effects in the northern hemisphere. The degassing history and volatile budget of this event are determined by measurements of pre-eruption and residual contents of sulfur, chlorine, and fluorine in the products of all phases of the eruption. In fissure eruptions such as Laki, degassing occurs in two stages: by explosive activity or lava fountaining at the vents, and from the lava as it flows away from the vents. Using the measured sulfur concentrations in glass inclusions in phenocrysts and in groundmass glasses of quenched eruption products, we calculate that the total accumulative atmospheric mass loading of sulfur dioxide was 122 Mt over a period of 8 months. This volatile release is sufficient to have generated approximately 250 Mt of H2SO4 aerosols, an amount which agrees with an independent estimate of the Laki aerosol yield based on atmospheric turbidity measurements. Most of this volatile mass (approximately 60 wt.%) was released during the first 1.5 months of activity. The measured chlorine and fluorine concentrations in the samples indicate that the atmospheric loading of hydrochloric acid and hydrofluoric acid was approximately 7.0 and 15.0 Mt, respectively. Furthermore, approximately 75% of the volatile mass dissolved by the Laki magma was released at the vents and carried by eruption columns to altitudes between 6 and 13 km. The high degree of degassing at the vents is attributed to development of a separated two-phase flow in the upper magma conduit, and implies that high-discharge basaltic eruptions such as Laki are able to loft huge quantities of gas to altitudes where the resulting aerosols can reside for months, or even 1-2 years. The atmospheric volatile contribution due to subsequent degassing of the Laki lava flow is only 18 wt.% of the total dissolved in the magma, and these emissions were confined to the lowest regions of the troposhere and therefore important only over Iceland. This study indicates that determination of the amount of sulfur degassed from the Laki magma batch by measurements of sulfur in the volcanic products (the petrologic method) yields a result which is sufficient to account for the mass of aerosols estimated by other methods.

Thordarson, T.↗
NASA NTRS1976

Martian volatiles - Their degassing history and geochemical fate

Implications of the Ar-40 content of the Martian atmosphere for Martian volatile history are considered. It is assumed that the potassium content of both Mars and earth is similar to that of normal chondrites, that Mars possesses a water content similar to that of normal chondrites, and that earth's water content is equal to or somewhat less than Mars'. A simple earth-analogous Mars degassing model is outlined in which the Martian surface volatile inventory is presumed to be identical to earth's, but scaled to the smaller mass and surface area of Mars. Physical storage of volatiles in the Martian regolith is examined along with the occurrence of volatile-containing mineral phases in the regolith, exospheric escape as a massive volatile sink, and the effect of the time history of degassing on the surface volatile inventory. Implications of earth's degassing history for Mars are assessed, and models describing the overall intensity of Mars degassing are presented. It is concluded that the maximum amounts of water and other volatiles that could be stored in the Martian regolith are marginally compatible with those required by the earth-analogous model, although a lower atmospheric Ar-40 concentration and regolith volatile inventory would be easier to reconcile with observational constraints.

Fanale, F. P.↗
NASA NTRS2016

Constraining the Sulfur Dioxide Degassing Flux from Turrialba Volcano, Costa Rica Using Unmanned Aerial System Measurements

Observed sulfur dioxide (SO2)mixing ratios onboard unmanned aerial systems (UAS) duringMarch 11-13, 2013 are used to constrain the three-day averaged SO2 degassing flux fromTurrialba volcanowithin a Bayesian inverse modeling framework. A mesoscale model coupled with Lagrangian stochastic particle backward trajectories is used to quantify the source-receptor relationships at very high spatial resolutions (i.e., b1 km). The model shows better performance in reproducing the near-surface meteorological properties and observed SO2 variations when using a first-order closure non-local planetary boundary layer (PBL) scheme. The optimized SO2 degassing fluxes vary from 0.59 +/- 0.37 to 0.83 +/- 0.33 kt d−1 depending on the PBL scheme used. These fluxes are in good agreement with ground-based gas flux measurements, and correspond to corrective scale factors of 8-12 to the posteruptive SO2 degassing rate in the AeroCom emission inventory. The maximum a posteriori solution for the SO2 flux is highly sensitive to the specification of prior and observational errors, and relatively insensitive to the SO2 loss term and temporal averaging of observations. Our results indicate relatively low degassing activity but sustained sulfur emissions from Turrialba volcano to the troposphere during March 2013. This study demonstrates the utility of low-cost small UAS platforms for volcanic gas composition and flux analysis.

Xi, Xin↗
NASA NTRS2021

Effect of volcanic emissions on clouds during the 2008 and 2018 Kilauea degassing events

Volcanic eruptions in otherwise clean environments are “natural experiments” wherein the effects of aerosol emissions on clouds and climate can be partitioned from meteorological variability and anthropogenic activities. In this work, we combined satellite retrievals, reanalysis products, and atmospheric modeling to analyze the mechanisms of aerosol–cloud interactions during two degassing events at the Kilauea volcano in 2008 and 2018. The eruptive nature of the 2008 and 2018 degassing events was distinct from long-term volcanic activity for Kilauea. Although previous studies assessed the modulation of cloud properties from the 2008 event, this is the first time such an analysis has been reported for the 2018 event and that multiple degassing events have been analyzed and compared at this location. Both events resulted in significant changes in cloud effective radius and cloud droplet number concentration that were decoupled from local meteorology and in line with an enhanced cloud albedo. However, it is likely that the effects of volcanic emissions on liquid water path and cloud fraction were largely offset by meteorological variability. Comparison of cloud anomalies between the two events suggested a threshold response of aerosol–cloud interactions to overcome meteorological effects, largely controlled by aerosol loading. In both events, the ingestion of aerosols within convective parcels enhanced the detrainment of condensate in the upper troposphere, resulting in deeper clouds than observed under pristine conditions. Accounting for ice nucleation on ash particles led to enhanced ice crystal concentrations at cirrus levels and a slight decrease in ice water content, improving the correlation of the model results with the satellite retrievals. Overall, aerosol loading, plume characteristics, and meteorology contributed to changes in cloud properties during the Kilauea degassing events.

Katherine H. Breen↗
NASA NTRSDate not supplied

Argon Isotopic Constraints on Planetary Degassing and the Evolution of Earth's Atmosphere: Insights from K-bearing Phases

An enduring question in planetary science is the nature of volatile degassing from rocky planets during their evolution. The reactive nature of planetary volatiles (e.g. H2O, CO2, N, H) make them difficult to directly track through time. Noble gases, like argon, can act as passive tracers of planetary processes, with isotopic ratios providing clues on planetary volatile inventories and fluxes. Previous studies [e.g. 1, 2] use Earth’s argon degassing history to constrain the growth of continental crust. However, that record is limited to the modern 40Ar/36Ar ratio of 298.56 [3] and three time slices recorded in hydrothermal quartz of the Archean Dresser formation [1]: from ~143 (3.5 Ga) to ~212 (2.7 Ga). Due to the paucity of data, partly a result of using nominally K-free minerals, the temporal evolution of atmospheric 40Ar/36Ar remains poorly constrained. K-bearing phases from igneous rocks, forming at high temperature and upper mantle or crustal conditions, are rarely considered viable for recording ancient atmospheric 40Ar/36Ar values. We show that this possible and a potential path to more precise records of ancient atmosphere by leveraging the radiogenic endmember of isotope correlation diagrams. An isochron of coeval biotite grains from the Bushveld Complex [4], with little indication of alteration or excess 40Ar, yield an initial 40Ar/36Ar value that matches the atmospheric 40Ar/36Ar value of ~228 at 2055 Ma in the model of [2]. In addition, new multi-mineral data from the Palisade Sill also match the modelled 40Ar/36Ar value of ~293 at 202 Ma, providing another tie point in the late Triassic. Combined, the Bushveld and Palisades samples provide two new constraints on the ancient atmosphere and help define the history of planetary degassing. These results demonstrate the possibility of accurately and precisely obtaining atmospheric information from igneous rocks, not exclusively K-free phases, thus providing a surplus of ways to reconstruct planetary atmospheres and processes. A robust atmospheric 40Ar/36Ar history also has practical uses and we explore the systematic offsets that arise from using a modern 40Ar/36Ar value in 40Ar/39Ar age calculations of old samples.

J. B. Setera↗
DOE OSTI2022

Slag Degassing for Electroslag Remelting Using Cold Start

The effect of slag degassing prior to cold start electroslag remelting (ESR) was investigated using various heat treatments of a commercial 40CaF2 – 30CaO – 30Al2O3 slag. The slag was either degassed in a vacuum heat treatment furnace or in a box furnace in air. Vacuum heat treatment included partial pressure of Ar gas. Several temperatures, ramp rates and/or holding times were investigated for each condition and the pressure was monitored for the heat treatment in the furnace with controlled atmosphere. A research scale 200 kg capacity ESR furnace was used for the experiments along with 1018 steel and 316 stainless steel electrodes. Significant differences in ingot quality were related to the sidewall and the presence of pores which were primarily located near the bottom of the ingot. Adjustments in the heat treatment temperature for heat treatment in air eventually led to an ingot quality near that obtained using slag degassed under vacuum and/or in a controlled atmosphere.

Detrois, Martin↗
NASA NTRS1984

Eruption age of an approximately 100,000-year-old basalt from Ar-40/Ar-39 analysis of partially degassed xenoliths

Eleven samples from five partially degassed Mesozoic granitic xenoliths and two late Pleistocene host basalt samples from Sawmill Canyon in Sierra Nevada, California, have been analyzed using stepwise Ar-40/Ar-39 dating techniques. The petrography and analytic techniques are described and the results are presented. Isotopic compositions of Ar released from the xenoliths in several extraction steps at temperatures below about 900 C were colinear in Ar-36/Ar-40 versus Ar-39/Ar-40 diagrams and defined isochrons, giving a mean age of degassing of 119,000 + or - 7000 yr. Ar-40 extracted at higher temperatures included ancient radiogenic Ar-40 that never diffused from the xenoliths during immersion in the magma. This Ar-40 caused an increase in the apparent age for the high-temperature extractions. The high precision of the eruption age determined by this method is comparable to that obtained elsewhere by conventional K/Ar dating of sanidine.

Gillespie, A. R.↗
NASA NTRS1988

Degassing history of Mars from Martian atmosphere samples

A comparison of the abundances of Ar-40 and He-4 (radiogenic) in various terrestrial planetary atmospheres provides clues to the volcanic and tectonic histories of the planets while the amount of primordial noble gases in the planetary atmospheres provides clues to the quantities of volatile rich materials captured by each planet. The noble gas contents of Mars, Earth, and Venus clearly show that the absolute abundances of isotopes of gases are directly proportional to the amounts of degassed CO2 into the planetary atmosphere. Several basic geological units can be seen on the global geological map of Mars. The enormous size of volcanic and tectonic structures of Mars, despite its smaller size, provide invaluable clues to the degassing history of Mars. Therefore, the collection of samples of Martian atmosphere and soil volatiles is imperative to understand the origin and evolution of the atmosphere and its interaction with the Martian surface. Surface properties of Martian rocks, soils, breccias, and regolith and their chemistry are also generic to any discussion on the origin and evolution of the atmosphere of Mars. The differences in absolute abundances of gases in the planetary atmospheres are amenable to many alternative interpretations. These alternative interpretations can be tested by imposing additional constraints derived from the isotopic results of noble gases in the atmospheres of the planets.

Rao, A. S. P.↗
NASA NTRS1994

Implications of noble gases in a recently recognized Martian meteorite (ALH84001) for the degassing history of Mars

For terrestrial planets, atmospheric compositions are not static, but evolve with time, in part due to degassing of the interior. Unfortunately, the evolution is slow enough that it is usually not observable on human timescales, or even on the timescales of rocks that preserve samples of Earth's ancient atmosphere. Preliminary results on a recently recognized Martian meteorite, ALH84001, indicate that it is a very old rock, and has a relatively high noble gas content suggestive of atmospheric incorporation, but with an isotopic composition slightly inconsistent with currently known Martian reservoirs. Hence, this rock may provide a sample of ancient Martian atmosphere, which can be used to test models of volatile evolution (in particular, degassing) on Mars. ALH84001 is a cumulate orthopyroxenite. Although originally classified as a diogenite, its oxygen isotopes, and several chemical and petrographic features, strong suggest that it is, like the SNC meteorites, Martian. A Sm-Nd crystallization age of 4.5 Ga has been reported. The meteorite is rich in noble gases, compared to most SNC's. In many respects the noble gases are typical of SNC meteorites. However, there are some subtle differences. In particular, the Xe isotopes in SNC meteorites can be explained as a mixture of Martian atmospheric Xe (as represented by glass in EETA 79001), the Xe in the dunite Chassigny (usually assumed to be representative of the Martian interior, and with lower (129)Xe/(132)Xe, (134)Xe/(132)Xe and (136)Xe/(132)Xe ratios), and later additions from known processes like fission, spallation and terrestrial contamination. The isotopic composition of ALH84001 is inconsistent (at greater than 2-3 sigma) with any mixture of those components. Even if no accumulation of fission Xe during the age of the rock is assumed, there is too little (136)Xe and (134)Xe for the amount of (129)Xe measured.

Swindle, T. D.↗
NASA NTRS1996

Sulfur, Chlorine and Fluorine Degassing and Atmospheric Loading by the Roza eruption, Columbia River Basalt Group, Washington

In this study we attempt to quantify the amount of S, Cl and F released by the 1300 cu km Roza member (approximately 14.7 Ma) of the Columbia River Basalt Group, which was produced by a moderate-size flood basalt eruption in the mid-Miocene. Our results are the first indication of the potential atmospheric SO2 yield from a flood basalt eruption, and indicate the mechanism by which flood basalt eruptions may have seriously affected the environment. Glass inclusions in phenocrysts and quenched glass in products from various stages of the eruption were analyzed for concentrations of S, Cl and F and major elements. Glass inclusions contain 1965 +/- 110 ppm S, 295 +/- 65 ppm Cl and 1310 +/- 110 ppm F. Groundmass glass of Roza dike selvages contains considerably lower concentrations: 1110 +/- 90 ppm S, 245 +/- 30 ppm Cl and 1020 +/- 25 ppm F. Scoria clasts from near vent deposits contain 665 +/- 75 ppm S, 175 +/- 5 ppm Cl and 950 +/- 20 ppm F, and the groundmass glass of lava selvages contains 520 +/- 30 ppm S, 190 +/- 30 ppm Cl and 890 +/- 55 ppm F. In crystalline lava, the concentrations are 195 ppm S, 100 ppm Cl and 830 ppm F. Volatile element concentrations in these samples represent the progress of degassing through the eruption and can be used to estimate the potential amount of the volatiles S, Cl and F released by the magma into the atmosphere, as well as to evaluate the amount liberated by various phases of the eruption. The total amount of volatiles released by the Roza eruption is estimated to have been approximately 12,420 MtSO2, approximately 710 MtHCI and approximately 1780 MtHF. The Roza magma liberated approximately 9620 MtSO, (77% of the total volatile mass released), approximately 400 MtHCI (56%) and approximately 1450 MtHF (81%) at the vents and lofted by the eruption columns to altitudes of 7-13 km. Degassing of the lava is estimated to have released an additional approximately 2810 MtSO2, approximately 310 MtHCI and approximately 330 MtHF. The Roza eruption is likely to have lasted for approximately 10 years, indicating an annual H2SO4-mass loading of approximately 1800 Mt. Thus, the atmospheric perturbations associated with the Roza eruption may have been of the magnitude predicted for a severe "nuclear" or "volcanic" winter, but lasting up to a decade or more.

Thordarson, Th.↗
NASA NTRSDate not supplied

Enabling more routine monitoring of volcanic CO2 degassing from space

“Volcanic aerosol impacts on satellite trace gas retrievals: enabling volcanic emission plume composition measurements to track evolving sub-surface magmatic conditions” ROSES 2019 IDS (Interdisciplinary Science), 2020-2023 (S. Broccardo, PI) Main hypothesis: Space-based observations of the CO2, SO2, and H2O emissions of passively degassing volcanoes, and the derived mass fluxes and their ratios, can be used to constrain a physical model of the pre-eruptive conditions of magmatic reservoirs and thereby improve our understanding of sub-surface processes.

Enabling↗