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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 13 (1998), S. 85-88 
    ISSN: 1573-4846
    Keywords: geyserite ; hyalite ; SEM ; SAXS ; microstructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The submicron structures of two natural hydrous forms of silica (geyserites from Iceland, hyalite from Valec CS) have been studied by scanning electron microscopy, small-angle and wide-angle X-ray scattering. All geyserites investigated are particulate with a nonuniform size distribution. These particles are arranged in spherical agglomerates, in chains or in helical patterns. The average diameters of the colloidal particles range between 200 nm and 2 μm depending on the texture of the samples. SAXS experiments have revealed the porous nature of the particles with inhomogeneities smaller than 10 nm. Based on the structural pecularities of the geyserites their origin is discussed as the result of forced condensation of silicic acid in an aqueous environment, particle agglomeration and sedimentation. The structural development including the textures is determined by the dynamics of the underlying processes: fast decompression and cooling of the saturated parent solutions and their transport. By contrast, hyalite is characterized by a homogeneous microstructure.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2013-04-22
    Print ISSN: 1742-6588
    Electronic ISSN: 1742-6596
    Topics: Physics
    Published by Institute of Physics
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  • 3
    Publication Date: 2019
    Description: 〈span〉The Upper Rhine Graben (URG), in the border area of southwestern Germany and eastern France, has suitable conditions for deep geothermal applications using enhanced geothermal systems (EGSs). Sandstone formations are used as geothermal reservoirs, where 〈span〉in situ〈/span〉 brines are in contact with the rock at the surfaces of fracture networks. Alteration reactions influence the fluid flow in the geothermal reservoir, and therefore, play a major role in the sustainable operation of the geothermal installation. For a better understanding of brine–rock interaction in EGSs, batch experiments at reservoir conditions have been performed with typical temperatures of 200 °C. Sandstone samples with a natural rock fabric were used. Sample surfaces represent rock fractures. Three different fluids with a composition close to natural URG brines have been used for the experimental series lasting up to 128 days: Na–Cl, Na–Ca–Cl, and Ca–Cl solutions all with an ionic strength of 2〈span〉m〈/span〉. Quartz dissolution and the removal of illite cement are the main reactions of the primary mineral assemblage, independently of the experimental solution composition. K-feldspar shows a high degree of dissolution only in the Ca–Cl solution. In general muscovite shows a high resistance to solution. The fluid compositions reflect the processes observed in the solid samples over time. On the sample surface massive amounts of zeolites precipitated during the hydrothermal experiments. In the Na–Cl series analcime is the sole zeolite phase. Analcime and wairakite occur on samples from experiments with Na–Ca–Cl solution. In the Ca–Cl series wairakite is the dominant zeolite phase, accompanied sparsely by epistilbite crystals. The zeolite phases have been identified and characterized by electron microprobe and synchrotron X-ray diffraction analyses. Reaction mechanisms have been derived from the observations of the solid and fluid samples. The main processes involve dissolution of quartz, illite, and partly K-feldspar, together with consumption of dissolved (earth-)alkali elements from solution. This results in the precipitation of zeolites, depending on the experimental solution composition. Based on the overall reactions, the volume of the solid phases increases, depending on the parent mineral. The observations in the experiments have been transferred to natural systems and are discussed in the context of URG geothermal systems. The experimental results show a large influence of brine–sandstone interaction on surfaces of fracture networks in EGSs. The observed processes have the potential to hamper the fluid flow and decrease the efficiency of geothermal installations.〈/span〉
    Print ISSN: 0935-1221
    Electronic ISSN: 1617-4011
    Topics: Geosciences
    Published by Schweizerbart
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  • 4
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  • 6
    Publication Date: 2012-10-08
    Description: Hielscherite, ideally Ca3Si(OH)6(SO4)(SO3)·11H2O, (IMA 2011-037) is the first ettringite-group mineral with essential sulfite. We have identified a continuous natural solid-solution series from endmember thaumasite, Ca3Si(OH)6(SO4)(CO3)·12H2O, to a composition with at least 77 mol.% endmember hielscherite. In this series, the SO3:CO3 ratio is variable, whereas the SO4 content remains constant. Compositions with more than 50 mol.% endmember hielscherite have only been found at Graulay quarry near Hillesheim in the western Eifel Mountains, Rhineland-Palatinate, where they occur with phillipsite-K, chabazite-Ca and gypsum in cavities in alkaline basalt. Sulfite-rich thaumasite has been found in hydrothermal assemblages in young alkaline basalts in two volcanic regions of Germany: it is widespread at Graulay quarry and occurs at Rother Kopf, Schellkopf and Bellerberg quarries in Eifel district; it has also been found at Zeilberg quarry, Franconia, Bavaria. Hielscherite forms matted fibrous aggregates up to 1 cm across and groups of acicular to prismatic hexagonal crystals up to 0.3 × 0.3 × 1.5 mm. Individual crystals are colourless and transparent with a vitreous lustre and crystal aggregates are white with a silky lustre. The Mohs hardness is 2–2½. Measured and calculated densities are Dmeans = 1.82(3) and Dcalc = 1.79 g cm−3. Hielscherite is optically uniaxial (−), ω = 1.494(2), ε = 1.476(2). The mean chemical composition of holotype material (determined by electron microprobe for Ca, Al, Si, and S and gas chromatography for C, H and N, with the S4+:S6+ ratio from the crystal-structure data) is CaO 27.15, Al2O3 2.33, SiO2 7.04, CO2 2.71, SO2 6.40, SO3 12.91, N2O5 0.42, H2O 39.22, total 98.18 wt.%. The empirical formula on the basis of 3 Ca atoms per formula unit is Ca3(Si0.73Al0.28)Σ1.01(OH)5.71(SO4)1.00(SO3)0.62(CO3)0.38(NO3)0.05·10.63H2O. The presence of sulfite was confirmed by crystal-structure analysis and infrared and X-ray absorption near edge structure spectra. The crystal structure of sulfite-rich thaumasite from Zeilberg quarry was solved by direct methods based on single-crystal X-ray diffraction data (R1 = 0.064). The structure of hielscherite was refined using the Rietveld method (Rwp = 0.0317). Hielscherite is hexagonal, P63, a = 11.1178(2), c = 10.5381(2) Å, V = 1128.06(4) Å3 and Z = 2. The strongest reflections in the X-ray powder pattern [(d,Å(I)(hkl)] are: 9.62(100)(010,100); 5.551(50)(110); 4.616(37)(012,102); 3.823(64)(112); 3.436(25)(211), 2.742(38)(032,302), 2.528(37)(123,213), 2.180(35)(042,402;223). In both hielscherite and sulfite-rich thaumasite, pyramidal sulfite groups occupy the same site as trigonal carbonate groups, with analogous O sites, whereas tetrahedral sulfate groups occupy separate positions. Hielscherite is named in honour of the German mineral collector Klaus Hielscher (b. 1957).
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 7
    Publication Date: 2012-10-01
    Description: Hielscherite, ideally Ca3Si(OH)6(SO4)(SO3)·11H2O, (IMA 2011-037) is the first ettringite-group mineral with essential sulfite. We have identified a continuous natural solid-solution series from endmember thaumasite, Ca3Si(OH)6(SO4)(CO3)·12H2O, to a composition with at least 77 mol.% endmember hielscherite. In this series, the SO3:CO3 ratio is variable, whereas the SO4 content remains constant. Compositions with more than 50 mol.% endmember hielscherite have only been found at Graulay quarry near Hillesheim in the western Eifel Mountains, Rhineland-Palatinate, where they occur with phillipsite-K, chabazite-Ca and gypsum in cavities in alkaline basalt. Sulfite-rich thaumasite has been found in hydrothermal assemblages in young alkaline basalts in two volcanic regions of Germany: it is widespread at Graulay quarry and occurs at Rother Kopf, Schellkopf and Bellerberg quarries in Eifel district; it has also been found at Zeilberg quarry, Franconia, Bavaria. Hielscherite forms matted fibrous aggregates up to 1 cm across and groups of acicular to prismatic hexagonal crystals up to 0.3 × 0.3 × 1.5 mm. Individual crystals are colourless and transparent with a vitreous lustre and crystal aggregates are white with a silky lustre. The Mohs hardness is 2–2½. Measured and calculated densities are Dmeans = 1.82(3) and Dcalc = 1.79 g cm−3. Hielscherite is optically uniaxial (−), ω = 1.494(2), ε = 1.476(2). The mean chemical composition of holotype material (determined by electron microprobe for Ca, Al, Si, and S and gas chromatography for C, H and N, with the S4+:S6+ ratio from the crystal-structure data) is CaO 27.15, Al2O3 2.33, SiO2 7.04, CO2 2.71, SO2 6.40, SO3 12.91, N2O5 0.42, H2O 39.22, total 98.18 wt.%. The empirical formula on the basis of 3 Ca atoms per formula unit is Ca3(Si0.73Al0.28)Σ1.01(OH)5.71(SO4)1.00(SO3)0.62(CO3)0.38(NO3)0.05·10.63H2O. The presence of sulfite was confirmed by crystal-structure analysis and infrared and X-ray absorption near edge structure spectra. The crystal structure of sulfite-rich thaumasite from Zeilberg quarry was solved by direct methods based on single-crystal X-ray diffraction data (R1 = 0.064). The structure of hielscherite was refined using the Rietveld method (Rwp = 0.0317). Hielscherite is hexagonal, P63, a = 11.1178(2), c = 10.5381(2) Å, V = 1128.06(4) Å3 and Z = 2. The strongest reflections in the X-ray powder pattern [(d,Å(I)(hkl)] are: 9.62(100)(010,100); 5.551(50)(110); 4.616(37)(012,102); 3.823(64)(112); 3.436(25)(211), 2.742(38)(032,302), 2.528(37)(123,213), 2.180(35)(042,402;223). In both hielscherite and sulfite-rich thaumasite, pyramidal sulfite groups occupy the same site as trigonal carbonate groups, with analogous O sites, whereas tetrahedral sulfate groups occupy separate positions. Hielscherite is named in honour of the German mineral collector Klaus Hielscher (b. 1957).
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 8
    Publication Date: 2015-12-01
    Print ISSN: 0304-4203
    Electronic ISSN: 1872-7581
    Topics: Geosciences
    Published by Elsevier
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  • 9
    Publication Date: 2019
    Description: 〈span〉The Upper Rhine Graben (URG), in the border area of southwestern Germany and eastern France, has suitable conditions for deep geothermal applications using enhanced geothermal systems (EGSs). Sandstone formations are used as geothermal reservoirs, where 〈span〉in situ〈/span〉 brines are in contact with the rock at the surfaces of fracture networks. Alteration reactions influence the fluid flow in the geothermal reservoir, and therefore, play a major role in the sustainable operation of the geothermal installation. For a better understanding of brine–rock interaction in EGSs, batch experiments at reservoir conditions have been performed with typical temperatures of 200 °C. Sandstone samples with a natural rock fabric were used. Sample surfaces represent rock fractures. Three different fluids with a composition close to natural URG brines have been used for the experimental series lasting up to 128 days: Na–Cl, Na–Ca–Cl, and Ca–Cl solutions all with an ionic strength of 2〈span〉m〈/span〉. Quartz dissolution and the removal of illite cement are the main reactions of the primary mineral assemblage, independently of the experimental solution composition. K-feldspar shows a high degree of dissolution only in the Ca–Cl solution. In general muscovite shows a high resistance to solution. The fluid compositions reflect the processes observed in the solid samples over time. On the sample surface massive amounts of zeolites precipitated during the hydrothermal experiments. In the Na–Cl series analcime is the sole zeolite phase. Analcime and wairakite occur on samples from experiments with Na–Ca–Cl solution. In the Ca–Cl series wairakite is the dominant zeolite phase, accompanied sparsely by epistilbite crystals. The zeolite phases have been identified and characterized by electron microprobe and synchrotron X-ray diffraction analyses. Reaction mechanisms have been derived from the observations of the solid and fluid samples. The main processes involve dissolution of quartz, illite, and partly K-feldspar, together with consumption of dissolved (earth-)alkali elements from solution. This results in the precipitation of zeolites, depending on the experimental solution composition. Based on the overall reactions, the volume of the solid phases increases, depending on the parent mineral. The observations in the experiments have been transferred to natural systems and are discussed in the context of URG geothermal systems. The experimental results show a large influence of brine–sandstone interaction on surfaces of fracture networks in EGSs. The observed processes have the potential to hamper the fluid flow and decrease the efficiency of geothermal installations.〈/span〉
    Print ISSN: 0935-1221
    Electronic ISSN: 1617-4011
    Topics: Geosciences
    Published by Schweizerbart
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  • 10
    Publication Date: 2018-03-01
    Description: We studied the effect of 973 K heating in argon atmosphere on the magnetic and structural properties of a magnetite-bearing ore, which was previously exposed to laboratory shock waves between 5 and 30 GPa. For this purpose magnetic properties were studied using temperature-dependent magnetic susceptibility, magnetic hysteresis and low-temperature saturation isothermal remanent magnetization. Structural properties of magnetite were analyzed using X-ray diffraction, high-resolution scanning electron microscopy and synchrotron-assisted X-ray absorption spectroscopy. The shock-induced changes include magnetic domain size reduction due to brittle and ductile deformation features and an increase in Verwey transition temperature due to lattice distortion. After heating, the crystal lattice is relaxed and apparent crystallite size is increased suggesting a recovery of lattice defects documented by a mosaic recrystallization texture. The structural changes correlate with modifications in magnetic domain state recorded by temperature-dependent magnetic susceptibility, hysteresis properties and low-temperature saturation isothermal remanent magnetization. These alterations in both, magnetic and structural properties of magnetite can be used to assess impact-related magnetic anomalies in impact structures with a high temperature overprint. © 2018. American Geophysical Union. All Rights Reserved.
    Electronic ISSN: 1525-2027
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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