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  • 1
    Publication Date: 2013-10-02
    Description: Hydrated evaporite minerals have the ability to hold large amounts of H 2 O, making them a potential source of H 2 O in cold, low- P H 2 O environments such as the surface of Mars. Many of these hydrated evaporite minerals experience a reversible change in hydration state in response to changes in temperature ( T ) and relative humidity (RH). Such phases may thus have the potential to interact with the martian atmosphere on a daily or seasonal basis. The Na 2 Mg(SO 4 ) 2 · n H 2 O system was previously thought to contain three hydrated phases: a decahydrate ( n = 10), konyaite ( n = 5), and blödite ( n = 4). We examined this system using temperature- and RH-controlled X-ray powder diffraction (XRD) methods, as well as temperature-controlled single-crystal X-ray diffraction. When blödite was exposed to sub-freezing conditions, T ≤ –10 °C, a new phase was produced ( n = 16, 52 wt%H 2 O). Similar low-temperature behavior has been documented in the MgSO 4 · n H 2 O system, through the presence of meridianiite ( Peterson et al. 2007 ). The hydration and dehydration behavior of phases in the Na 2 Mg(SO 4 ) 2 · n H 2 O system was evaluated with powder XRD from –30 to 〉25 °C and from ~99 to near 0% RH, and single-crystal XRD data were collected for the n = 16 phase at –120 °C. The 16-hydrate is triclinic, space group P , with unit-cell parameters a = 6.5590(12), b = 6.6277(14), c = 14.441(3) Å, α = 87.456(15)°, β = 79.682(15)°, = 65.847(13)°, and a unit-cell volume of 563.3(2) Å 3 . The existence of this new phase at low temperatures, its high hydration state, and its ability to form reversibly from blödite all suggest that if phases in this system exist on the martian surface, they will participate in the Mars H 2 O cycle.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 2
    Publication Date: 2013-10-01
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 3
    Publication Date: 2019-07-20
    Description: Recent work suggests that the mineralogical sequence of the Murray formation at Gale crater may have resulted from diagenetic alteration after sedimentation, or deposition in a stratified lake with oxic surface and anoxic bottom waters. Fe-containing clay minerals are common both at Gale crater, and throughout the Noachian-aged terrains on Mars. These clay minerals are primarily ferric (Fe3+), and previous work suggests that these ferric clay minerals may result from alteration of ferrous (Fe2+) smectites that were oxidized after deposition. The detection of trioctahedral smectites at Gale crater by CheMin suggests Fe2+ smectite was also deposited during the early Hesperian. However, due to their sensitivity to oxygen, Fe2+ smectites are difficult to analyze on Earth and very few saponite dissolution rates exist in the literature. To the best of our knowledge, no experiments have measured the dissolution rates of ferrous saponites under oxidizing and reducing conditions. In order to better understand the characteristics of water-rock interaction at Gale crater, particularly the oxidation state, we report our results to date on ongoing syntheses of ferrous and magnesium saponites and dissolution experiments of natural saponite under ambient conditions. Future experiments will include the dissolution of synthetic ferric, ferrous, and magnesium saponites under oxidizing and anoxic conditions at a range of pH values.
    Keywords: Lunar and Planetary Science and Exploration
    Type: LPI Contrib. No. 2132 , JSC-E-DAA-TN66074 , Lunar and Planetary Science Conference (LPSC 2019); 18ý22 Mar. 2019; The Woodlands, TX; United States
    Format: application/pdf
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