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  • Mineralogical Society of America  (25)
  • Nature Publishing Group  (1)
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  • 1
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] The present observations are from samples BCSCO-a and BCSCO-b of Hazen et al.2. All selected-area electron diffraction microscopy (SAED), X-ray analytical electron microscopy (AEM), and high-resolution transmission electron microscopy (HRTEM) experiments were performed with a Philips 420 ...
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Publikationsdatum: 2016-04-02
    Print ISSN: 0003-004X
    Digitale ISSN: 1945-3027
    Thema: Geologie und Paläontologie
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Publikationsdatum: 2015-02-13
    Beschreibung: In ferruginous soils, nano- to microscale hematite (α-Fe 2 O 3 ) plays a central role in redox processes and contaminant cycling. Hematite is known to incorporate structural OH – and water, and the requisite charge balance is achieved by iron vacancies. Prior researchers have suggested that the defective hematite structures form unique phases called "protohematite" and "hydrohematite." Infrared and Raman spectroscopic studies have assigned a lower-symmetry space group to "hydrohematite" ( R 3 c ) relative to that of stoichiometric hematite ( R c ). However, the existence and structure of these phases have been contentious, largely due to the lack of in situ X-ray diffraction data Here we present a new structure refinement for "hydrohematite" precipitated hydrothermally at 200 °C in a monoclinic space group ( I 2/ a ) using time-resolved synchrotron X-ray diffraction (TR-XRD) data collected during the in situ hydrothermal precipitation of akaganeite and its transformation to stoichiometric hematite. Distinct peak splitting was observed in the "hydrohematite" diffraction patterns, indicating a violation of the threefold rotational symmetry. A monoclinic unit cell with parameters of a = 7.3951(10), b = 5.0117(5), c = 5.4417(7) Å, β = 95.666(5)° provided a good fit and significant reduction in 2 and R wp relative to space group R c . Rietveld analyses revealed that water concentrations in the first-formed crystals of "hydrohematite" were comparable to water contents of akaganeite and goethite. Thus, the hydrothermal transformation of akaganeite to "hydrohematite" is promoted not by dehydration but by reconstruction of the oxygen framework.
    Print ISSN: 0003-004X
    Digitale ISSN: 1945-3027
    Thema: Geologie und Paläontologie
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  • 4
    Publikationsdatum: 2015-10-02
    Beschreibung: A structural derivative of quartz with the composition Mg 0.5 AlSiO 4 has been grown from glass and characterized using synchrotron X-ray diffraction (XRD), transmission electron microscopy (TEM), and 29 Si nuclear magnetic resonance (NMR) spectroscopy. Rietveld analysis of the XRD data indicates that the framework of Mg 0.5 AlSiO 4 is isostructural with α-quartz, rather than β-quartz, as is consistent with previous theoretical modeling ( Sternitzke and Müller 1991 ). Al and Si exhibit long-range disorder over the framework tetrahedral sites, indicated by the absence of the superlattice reflections corresponding to the doubling of c relative to that of quartz. Nevertheless, 29 Si NMR measurements show that Al and Si exhibit partial short-range order with an ordering degree of 56%. Electron diffraction reveals superlattice reflections indicative of doubled periodicities along the a -axes. Fourier electron density maps show that Mg occupies channel sites that each are bonded to six O atoms, in contrast to the tetrahedral coordination of Li in the β-quartz-type framework for β-eucryptite, LiAlSiO 4 . Furthermore, the concentrations of Mg in adjacent channels are different, resulting in framework distortions that generate the superstructures along a .
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    Thema: Geologie und Paläontologie
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  • 5
    Publikationsdatum: 2016-02-03
    Beschreibung: Synchrotron powder X-ray diffraction and scanning electron microscopy examinations of manganese oxide concretions/nodules (~0.3–1.0 mm diameter) from ODP Site 1262 on Walvis Ridge in the Southeastern Atlantic Ocean revealed that they consist primarily of the layered Mn oxide phase jianshuiite [(Mg,Mn,Ca)Mn 3 4+ O 7 ·3H 2 O]. The nodules are from an interval with severe carbonate dissolution that represents the Paleocene/Eocene (P/E) thermal maximum (~55.8 Ma). Most nodules from the middle of the carbonate dissolution interval contain internal open space, and consist almost entirely of euhedral plate-like jianshuiite crystals, 2–4 μm in diameter and ~0.1–0.5 μm thick. Backscattered electron images and energy-dispersive X-ray analyses revealed stacks of interleaved Al-rich and Al-poor jianshuiite crystals in some nodules. The crystals in other nodules contain predominantly Mg (with trace K and Al) in addition to Mn and O, making them near "end-member" jianshuiite. Rietveld refinements in space group R confirmed the isostructural relationship between jianshuiite and chalcophanite, with Mg occupying the interlayer position above and below the vacant sites in the Mn/O octahedral sheet, and coordinated to 3 octahedral layer O atoms (1.94 Å) and 3 interlayer water O atoms (2.13 Å). Final refined occupancy factors suggest that small quantities of Ni and possibly Mn 2+ are located on the Mg site. The transient appearance of the Mg-rich birnessite-like phase jianshuiite, probably abiotically produced, must indicate an exceptional transient change in the chemistry of the pore fluids within deep ocean sediments directly following the P/E boundary, possibly as a result of decreasing oxygen levels and pH, followed by a return to pre-event conditions.
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    Digitale ISSN: 1945-3027
    Thema: Geologie und Paläontologie
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  • 6
    Publikationsdatum: 2014-10-02
    Beschreibung: Time-resolved synchrotron X-ray powder diffraction data were used to investigate the dehydration behavior of the chalcophanite (ZnMn 3 O 7 ·3H 2 O) structure from 300 to 1060 K. Rietveld refinements revealed two obvious phase changes, at ~450 and ~950 K, corresponding to the dehydration of chalcophanite followed by transformation to a spinel structure (Mn-hetaerolite). Only small changes were observed in the chalcophanite unit cell from RT to ~438 K; the volume increased by ~0.8%, mostly caused by thermal expansion of ~0.5% along c . Above ~427 K, the interlayer water molecules were lost, resulting in a collapse of the interlayer spacing from ~7 to ~4.8 Å. The newly formed anhydrous phase (ZnMn 3 O 7 ) retained chalcophanite’s R space group and a dimension, but the c dimension decreased from ~21 to 14.3 Å, and the Zn coordination changed from octahedral to tetrahedral. Above ~775 K the anhydrous chalcophanite began to transform to a spinel structure, corresponding to a Mn-rich hetaerolite [(Zn 0.75 Mn 2+ 0.25 )Mn 2 3+ O 4 ]. By ~973 K the transformation was complete. The diffraction patterns did not show a significant increase in background during the transformation, indicating that the reaction did not involve transient amorphization. The phase change was likely triggered by loss of 1.25 of seven O atoms in the original anhydrous chalcophanite structure with a corresponding reduction of Mn 4+ to Mn 3+ and Mn 2+ .
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    Thema: Geologie und Paläontologie
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  • 7
    facet.materialart.
    Unbekannt
    Mineralogical Society of America
    Publikationsdatum: 2016-05-03
    Beschreibung: Charles Darwin analogized the diversification of species to a Tree of Life. This metaphor aligns precisely with the taxonomic system that Linnaeus developed a century earlier to classify living species, because an underlying mechanism—natural selection—has driven the evolution of new organisms over vast timescales. On the other hand, the efforts of Linnaeus to extend his "universal" organizing system to minerals has been regarded as an epistemological misfire that was properly abandoned by the late nineteenth century. The mineral taxonomies proposed in the wake of Linnaeus can be distinguished by their focus on external character (Werner), crystallography (Haüy), or chemistry (Berzelius). This article appraises the competition among these systems and posits that the chemistry-based Berzelian taxonomy, as embedded within the widely adopted system of James Dwight Dana, ultimately triumphed because it reflects Earth’s episodic but persistent progression with respect to chemical differentiation. In this context, the pioneering work of Hazen et al. (2008) in mineral evolution reveals that even the temporal character of the phylogenetic Tree of Life is rooted within a Danan framework for ordering minerals.
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    Thema: Geologie und Paläontologie
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  • 8
    facet.materialart.
    Unbekannt
    Mineralogical Society of America
    Publikationsdatum: 2017-05-02
    Print ISSN: 0003-004X
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    Thema: Geologie und Paläontologie
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  • 9
    Publikationsdatum: 2012-08-01
    Beschreibung: Birnessite and other charged layered manganese oxide minerals exhibit interlayers with variable cation-water behavior that controls many environmentally important cation exchange, adsorption, and redox processes. The occurrence of birnessite phases as fine-grained materials with corresponding high-surface areas makes them effective in controlling soil sediment and groundwater compositions, but difficult to structurally characterize using conventional analytical methods. Molecular simulations provide an alternative approach in which many details of bulk and interlayer structure can be ascertained to supplement and interpret the experimental findings. Classical and electronic structure methods are used to evaluate Na-, K-, and Ba-birnessite phases. Computational results compare favorably with structures obtained by synchrotron X-ray diffraction and difference electron Fourier mapping of the interlayer region. Based on the analysis of the 1 ns atomic trajectories, dynamics of water molecules is enhanced in the interlayer of K-birnessite relative to the limited motion of water molecules and cations in the other birnessite phases. Molecular dynamics simulations of ranciéite, a complex layered manganese oxide having octahedral vacancies, indicate multiple sites for Ca 2+ in the interlayer. In addition to manganese layer charge and layer structure, the hydration enthalpy for the interlayer cation affects the structure and dynamics of the interlayer in birnessite minerals.
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    Thema: Geologie und Paläontologie
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  • 10
    Publikationsdatum: 2013-03-30
    Beschreibung: To measure the uptake of radioactive Cs in soils that are rich in Mn oxides, we applied time-resolved synchrotron X-ray diffraction (TR-XRD), inductively coupled plasma-mass spectrometry (ICP-MS), and analytical scanning electron microscopy (SEM) to determine the kinetics and mechanisms of aqueous Cs substitution in the phyllomanganate hexagonal H-birnessite at pH values ranging from 3 to 10. We observed that the rate of Cs cation exchange into hexagonal H-birnessite exhibited only a weak dependence on pH, but the total amount of Cs loading in the interlayer region increased dramatically above pH 6.5. The increase in Cs content at higher pH may be attributed to the increasingly negative charge on the Mn-O octahedral sheets and perhaps to a structural change toward triclinic symmetry with high pH. Dissolution at low pH may have inhibited Cs sequestration. Our work supports delamination-reassembly as a mechanism of cation exchange.
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    Thema: Geologie und Paläontologie
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