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  • LUNAR AND PLANETARY EXPLORATION  (27)
  • Hydrous Minerals  (1)
  • Troilite  (1)
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Publisher
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Space science reviews 92 (2000), S. 177-200 
    ISSN: 1572-9672
    Keywords: Solar Nebula ; Kinetics ; Thermochemistry ; Magnetite ; Troilite ; Water ; Hydrous Minerals ; Hydration ; Oxidation ; Volatiles ; Serpentine ; Talc ; Brucite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Thermochemical equilibrium calculations predict gas phase, gas-grain, and solid phase reactions as a function of pressure and temperature in the solar nebula. However, chemical reactions proceed at different rates, which generally decrease exponentially with decreasing temperature. At sufficiently low temperatures (which vary depending on the specific reaction) there may not have been enough time for the predicted equilibrium chemistry to have taken place before the local environment cooled significantly or before the gaseous solar nebula was dispersed. As a consequence, some of the high temperature chemistry established in sufficiently hot regions of the solar nebula may be quenched or frozen in without the production of predicted low temperature phases. Experimental studies and theoretical models of three exemplary low temperature reactions, the formation of troilite (FeS), magnetite (Fe3O4), and hydrous silicates, have been done to quantify these ideas. A comparison of the chemical reaction rates with the estimated nebular lifetime of 0.1-10 million years indicates that troilite formation proceeded to completion in the solar nebula. Magnetite formation was much slower and only thin magnetite rims could have formed on metal grains. Hydrous silicate formation is predicted to be even slower, and hydrous silicates in meteorites and interplanetary dust particles probably formed later on the parent bodies of these objects, instead of in the solar nebula.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2011-08-24
    Description: We present a new method for determining the abundance of sulfur dioxide below the clouds of Venus. Absorption by the 3nu3 band of SO2 near 2.45 microns has been detected in high-resolution spectra of the night side of Venus recorded at the Canada-France Hawaii telescope in 1989 and 1991. The inferred SO2 abundance is 130 +/- 40 ppm at all observed locations and pertains to the 35-45 km region. These values are comparable to those measured by the Pioneer Venus and Venera 11/12 entry probes in 1978. This stability stands in contrast to the apparent massive decrease in SO2 observed at the cloud tops since these space missions. These results are consistent with laboratory and modeling studies of the SO2 destruction rates in the lower atmosphere of Venus. The new spectroscopic technique presented here allows a remote monitoring of the SO2 abundance below the clouds, a likely tracer of Venusian volcanism.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Geophysical Research Letters (ISSN 0094-8276); 20; 15; p. 1587-1590.
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  • 3
    Publication Date: 2011-08-24
    Description: A comprehensive review of the chemistry and spectroscopy of the Uranian atmosphere is presented by means of earth-based, earth-orbital, and Voyager 2 observations covering the UV, visible, infrared, and radio wavelength regions. It is inferred from these observations, in concert with the average density of about 1.3 g/cu cm, that the Uranian atmosphere is enriched in heavy elements relative to solar composition. Pre-Voyager earth-based observations of CH4 bands in the visible region and Voyager radio occultation data imply a CH4/H2 volume mixing ratio of about 2 percent corresponding to an enrichment of approximately 24 times the solar value of 0.000835. In contrast to CH4, microwave observations indicate an apparent depletion of NH3 in the 155-to-200-K region of the atmosphere by 100 to 200 times relative to the solar NH3/H2 mixing ratio of -0.000174. It is suggested that the temporal and latitudinal variations deduced for the NH3/H2 mixing ratio in this region of the Uranian atmosphere are due to atmospheric circulation effects.
    Keywords: LUNAR AND PLANETARY EXPLORATION
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  • 4
    Publication Date: 2013-08-29
    Description: A knowledge of the original volatile endowment of Mars is essential for any discussion of atmospheric loss on this planet. Cosmochemical models which postulate that planetary bulk compositions and volatile contents were controlled by the radial temperature profile in the solar nebula, and estimated bulk compositions based on the assumption that Mars is the parent body for the SNC meteorites predicts that Mars is volatile-rich. However, contrary views can also be found. For illustrative purposes, it is assumed that Mars was volatile-rich initially like the Earth. Taking terrestrial volatiles as the sum of the atmospheric, crustal, and oceanic volatiles and assuming that Mars accreted with the same volatile content on a g/g basis, the volatile endowments for an Earth-like Mars correspond to approximately 14 bars CO2, 800 mbars N2, and 1.2 km H2O. Subsequent topics discussed are: composition of outgassing volatiles; rates of present day atmospheric-surface reactions; constraints on CO2 loss via carbonate formation; constraints on H2O loss; and loss of other volatiles.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Workshop on the Martian Surface and Atmosphere Through Time; p 49-50
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  • 5
    Publication Date: 2011-08-19
    Description: Laboratory rate data for the reaction between SO2 and calcite to form anhydrite are presented. If this reaction rate represents the SO2 reaction rate on Venus, then all SO2 in the Venusian atmosphere will disappear in 1.9 Myr unless volcanism replenishes the lost SO2. The required volcanism rate, which depends on the sulfur content of the erupted material, is in the range 0.4-11 cu km of magma erupted per year. The Venus surface composition at the Venera 13, 14, and Vega 2 landing sites implies a volcanism rate of about 1 cu km/yr. This geochemically estimated rate can be used to determine if either (or neither) of two discordant geophysically estimated rates is correct. It also suggests that Venus may be less volcanically active than the earth.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Nature (ISSN 0028-0836); 337; 55-58
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  • 6
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    Unknown
    In:  CASI
    Publication Date: 2013-08-29
    Description: During the MSATT workshop in Boulder, CO, several participants emphasized the importance of constraints on the composition and temporal evolution of outgassed volatiles on Mars. I present the results of some preliminary calculations that model the composition of volcanic gases as a function of temperature, pressure, oxygen fugacity, and quench function of temperature. These results can be used in combination with cosmochemical models for the accretion of Mars to assess the plausibility of different atmospheric compositions during the planet's early history.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Papers Presented to the Workshop on the Evolution of the Martian Atmosphere; p 9-11
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  • 7
    Publication Date: 2016-06-07
    Description: A review of the applications of chemical thermodynamics and chemical kinetics to planetary atmospheres research during the past four decades is presented with an emphasis on chemical equilibrium models and thermochemical kinetics. Several current problems in planetary atmospheres research such as the origin of the atmospheres of the terrestrial planets, atmosphere-surface interactions on Venus and Mars, deep mixing in the atmospheres of the gas giant planets, and the origin of the atmospheres of outer planet satellites all require laboratory data on the kinetics of thermochemical reactions for their solution.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: NASA, Goddard Space Flight Center, First International Conference on Laboratory Research for planetary Atmospheres; p 267-302
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  • 8
    Publication Date: 2019-01-25
    Description: Thermochemical and photochemical reactions between surface minerals and present-day atmospheric constituents are predicted to produce microscopic effects on the surface of mineral grains. Relevant reactions hypothesized in the literature include conversions of silicates and volcanic glasses to clay minerals, conversion of ferrous to ferric compounds, and formation of carbonates, nitrates, and sulfates. These types of surface-atmosphere weathering of minerals, biological potential of the surface environment, and atmospheric stability in both present and past Martian epochs. It is emphasized that the product of these reactions will be observable and interpretable on the microscopic surface layers of Martian surface rocks using modern techniques with obvious implications for sample return from Mars. Macroscopic products of chemical weathering reactions in past Martian epochs are also expected in Martian surface materials. These products are expected not only as a result of reactions similar to those proceeding today but also due to aqueous reactions in past epochs in which liquid water was putatively present. It may prove very difficult or impossible, however, to determine definitively from the relic macroscopic product alone either the exact weathering process which led to its formation of the identity of its weathering parent mineral. The enormous advantages of studying the Martian chemical weathering by investigating the microscopic products of present-day chemical reactions on sample surfaces are very apparent.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Workshop on Mars Sample Return Science; p 141
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  • 9
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    Unknown
    In:  Other Sources
    Publication Date: 2019-06-28
    Description: An evaluation is made of extant data on chondrite oxidation states and intrinsic O fugacities. A variety of oxidation states are exhibited by the chondritic meteorites; petrologic and chemical data may be used to arrange the major chondrite groups in order of oxidation state. The intrinsic O fugacity measurements on chondrite whole-rock samples are noted to display a corresponding ordering of oxidation states. Metamorphosed chondrites and igneous meteorites that were substantially altered by metamorphic reactions, outgassing, and igneous processes may preserve information on the oxidation state and size of their parent bodies.
    Keywords: LUNAR AND PLANETARY EXPLORATION
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  • 10
    Publication Date: 2019-06-28
    Description: The maintenance of the global H2SO4 clouds on Venus requires volcanism to replenish the atmospheric SO2 which is continually being removed from the atmosphere by reaction with calcium minerals on the surface of Venus. The first laboratory measurements of the rate of one such reaction, between SO2 and calcite (CaCO3) to form anhydrite (CaSO4), are reported. If the rate of this reaction is representative of the SO2 reaction rate at the Venus surface, then we estimate that all SO2 in the Venus atmosphere (and thus the H2SO4 clouds) will be removed in 1.9 million years unless the lost SO2 is replenished by volcanism. The required rate of volcanism ranges from about 0.4 to about 11 cu km of magma erupted per year, depending on the assumed sulfur content of the erupted material. If this material has the same composition as the Venus surface at the Venera 13, 14 and Vega 2 landing sites, then the required rate of volcanism is about 1 cu km per year. This independent geochemically estimated rate can be used to determine if either (or neither) of the two discordant (2 cu km/year vs. 200 to 300 cu km/year) geophysically estimated rates is correct. The geochemically estimated rate also suggests that Venus is less volcanically active than the Earth.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: NASA-CR-183039 , NAS 1.26:183039
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