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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 55 (1999), S. 301-309 
    ISSN: 1572-8943
    Keywords: dehydroxylation ; goethite ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The kinetics of thermal dehydroxylation of aluminuous goethites [1] synthesised from a ferrous salt has been re-examined using the general reaction order kinetic law. The utilised data processing was based on the procedures employed by dissolution kinetics. Recalculation of the activation energies EA of the dehydroxylation yielded the values 130, 132, 128, and 123 kJ mol−1 for pure goethite, goethite with 10, 20, and 30 mol% Al substitution, respectively. The values of EA are in a good agreement with those given for goethite in literature. The EA values are linearly related with the chemically bound excess H2O/OH− in the crystal lattice that is apparently influenced by Al substitution.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2011-03-01
    Description: The aggregation of three cationic dyes (CD), crystal violet (CV), Nile blue (NB) and rhodamine B (RB) in aqueous solution was studied by visible absorption spectrophotometry and compared with methylene blue (MB). The distribution of the dye species (monomers, dimers, trimers, and tetramers) in aqueous solutions with different concentrations of dye was calculated using equilibrium stepwise aggregation constants Kn. These cationic dyes were intercalated into montmorillonite (SAz-1) and its reduced charge form (RC-SAz(210)) prepared by heating lithium montmorillonite (Li/SAz-1) at 210{degrees}C. The fluorescence of fully saturated CD/SAz and low-CD loaded CD/RC-SAz(210) complexes was studied. Visible absorption spectra of CD aqueous solutions and visible absorption spectra and X-ray diffraction patterns (d001) of the CD/SAz and CD/RC-SAz(210) solid complexes were obtained and evaluated. Large fluorescence intensities were found for CV/RC-SAz(210) and NB/RC-SAz(210) complexes in the same way as for the complex of methylene blue with reduced-charge montmorillonite MB/RCM(210) described previously.
    Print ISSN: 0009-8558
    Electronic ISSN: 1471-8030
    Topics: Geosciences
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  • 3
    Publication Date: 2014-03-20
    Description: A multidisciplinary correlation of the Devonian–Carboniferous (D–C) boundary sections from the Moravian Karst (Czech Republic) and the Carnic Alps (Austria), based on conodont and foraminifer biostratigraphy, microfacies analysis, field gamma-ray spectroscopy (GRS), carbon isotopes and element geochemistry, is presented in this paper. The study is focused on the interval from the Middle Palmatolepis gracilis expansa Zone (Late Famennian) to the Siphonodella sandbergi Zone (Early Tournaisian). In Lesní lom (Moravian Karst), a positive 13 C excursion in the Bisphatodus costatus – Protognathodus kockeli Interregnum from a distinct laminated carbonate horizon is correlated with a carbon isotope excursion from the Grüne Schneid section of the Carnic Alps and is interpreted as the equivalent of the Hangenberg black shales and a local expression of the global Hangenberg Event sensu stricto . Higher up at both sections, a significant increase in the terrigenous input, which is inferred from the GRS signal and elevated concentrations of terrigenous elements (Si, Ti, Zr, Rb, Al, etc.), provides another correlation tieline and is interpreted as the equivalent of the Hangenberg sandstone. Both horizons are discussed in terms of relative sea-level fluctuations and palaeoceanographic changes. Recent studies show that conodont biostratigraphy is facing serious problems associated with the taxonomy of the first siphonodellids, their dependence on facies and discontinuous occurrences of protognathodids at the D–C boundary. Therefore, the correlative potential of geochemical and petrophysical signatures is high and offers an alternative for the refining of the problematic biostratigraphic division of the D–C boundary.
    Print ISSN: 0016-7568
    Electronic ISSN: 1469-5081
    Topics: Geosciences
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  • 4
    Publication Date: 2011-09-16
    Description: The adsorption of methylene blue (MB) on montmorillonite from acid solutions has not yet been studied in detail. In this paper the adsorption of this dye on Ca/SAz montmorillonite from 0.32, 0.80 and 1.60 M HCl solutions at ambient temperature and after 2 hours leaching was carefully studied and evaluated. Under the above conditions the MB/SAz intercalates formed are practically insoluble. In contrast to the adsorption of methylene blue on montmorillonite from aqueous solutions, the adsorption from acid solutions consists of two adsorption waves. The intercalated samples from the first and second waves were studied using X-ray powder diffraction (XRD), FTIR, Vis spectroscopy, and scanning electron microscopy (SEM) equipped with a microprobe system. The adsorption of MB in the first wave is attributed to ion exchange of the dye cationic species (MB+, [IMG]f1.gif" ALT="Formula" BORDER="0"〉, H-aggregates, MBH2+ and H+) for the original interlayer cations of montmorillonite. The percentages of MBH2+ and H+ based on total adsorbed MB were estimated for varying HCl concentrations. The second adsorption wave is linked to the precipitation of MB species on the outer MB/SAz surface.
    Print ISSN: 0009-8558
    Electronic ISSN: 1471-8030
    Topics: Geosciences
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  • 5
    Publication Date: 2014-12-04
    Description: This study reports on a ~ 150 m thick macrofossil-barren sequence of siliciclastic sediments from a Burdigalian age (Early Miocene) freshwater lake. The lake was located within an incipient rift system of the Most Basin in the Ohře (Eger) Graben, which was part of the European Cenozoic Rift System, and had an original area of 1000 km 2 . Sediments from the HK591 core that cover the entire thickness of the lake deposits and some of the adjacent stratigraphic units were analysed by X-ray fluorescence spectroscopy (a proxy for element composition) and magnetic polarity measurement. The element proxies were subjected to frequency analysis, which provided estimated sedimentation rates, and allowed for sediment dating by magnetostratigraphy and orbital tuning of the age model. Based on the resulting age model and the known biostratigraphy, the lake was present between 17.4 and 16.6 Ma, which includes the onset of the Miocene Climatic Optimum in the latest Early Miocene. The identification of orbital forcing (precession, obliquity and short eccentricity cycles) confirms the stability of the sedimentary environment of the perennial lake in an underfilled basin. The dating allowed the sediment record to be interpreted in the context of the current knowledge of the European climate during that period. The stability of the sedimentary environment confirms that precipitation was relatively stable over the period recorded by the sediments.
    Print ISSN: 0016-7568
    Electronic ISSN: 1469-5081
    Topics: Geosciences
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  • 6
    Publication Date: 2014-07-11
    Description: The iron chemistry of aluminosilicates can markedly affect their adsorption properties due to possible changes in surface charge upon exposure to a variety of processes in the environment. One of these processes is chemical leaching, but to date little has been reported on the susceptibility of structural Fe to chemical leaching. The purpose of the current study was to determine the effects of solution pH on the stability of structural Fe in kaolinites, illite, and bentonite and the potential for formation of ancillary (oxyhydr)oxides. Structurally bound Fe does not participate in sorption properties but Fe that is released and phase transformed during leaching could take part in adsorption processes and form complexes and/or covalent bonds via Fe ions. Five different Fe-bearing clay minerals were treated in 0.5 M and 2 M HCl, distilled H 2 O, 0.1 M KCl, and 0.5 M KHCO 3 for 24 h. The amount of Fe leached varied from 10 μg g –1 (for 0.1 M KCl) to 10 4 μg g –1 (for 2 M HCl) depending on the leaching agents. Acidic and water treatments indicated a relative independence of leached Fe on the initial Fe content in the clay and, conversely, a heavy dependence on the crystallinity of initial Fe phases. Well crystallized Fe(III) was stable during the leaching process, while poorly crystallized and amorphous Fe(III) phases were less stable, forming new ion-exchangeable Fe 3+ particles. Under alkaline conditions, no relation between Fe crystallinity and mobility was found. The structural and surface changes resulting from leaching processes were identified by equilibrium adsorption isotherms. In kaolinite, the specific surface area ( S BET ) and porosity changed independently of Fe leaching due to the stability and crystallinity of Fe. In bentonite, the number of micropores was reduced by their partial saturation with Fe 3+ particles caused by poorly crystallized and more reactive Fe forms during the leaching process. Potential phase transformations of Fe were characterized by the voltammetry of microparticles; well crystallized Fe(III) oxides remained stable under leaching conditions, while poorly crystallized and amorphous Fe(III) phases were partially dissolved and transformed to reactive Fe 3+ forms.
    Print ISSN: 0009-8604
    Electronic ISSN: 1552-8367
    Topics: Geosciences
    Published by Clay Minerals Society
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  • 7
    Publication Date: 2005-03-31
    Print ISSN: 1618-2642
    Electronic ISSN: 1618-2650
    Topics: Chemistry and Pharmacology
    Published by Springer
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  • 8
    Publication Date: 2019
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
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  • 9
    Publication Date: 2017-01-12
    Description: Silicified Agathoxylon -type wood of Late Palaeozoic age was characterized by means of cathodoluminescence (CL) and LA-ICP-MS of the quartz mass, which was found to contain wakefieldite, characterized by electron-microprobe (EMP) analysis, Raman microspectroscopy and X-ray diffraction. Although former organic matter is almost absent, plant anatomy served as the template for the quartz mass texture. Two generations of quartz mass were distinguished; the large proportion of the silicified wood consisting of brownish α-quartz with a dark reddish CL emission, and the minor portion of whitish ‘leached’ wood with a short-lived (transient) blue CL. On the outer edge, a silicified texture of formerly slightly humified wood also emits a dark reddish CL. Likely the wood specimen has been fossilized and diagenetically altered in several steps. The marginal part had been humified (reductively degraded) before the initial stages of silicification. The LA-ICP-MS analyses revealed chemical differences in all three distinct parts. The quartz mass relatively enriched in REEs and As and giving the dark reddish CL is interpreted as a primary diagenetic mineral mass. Whitish zones relatively depleted in U and V, and enriched in Al, Li, Rb, Cu, and Sr producing the blue CL would then be a secondary diagenetic overprint. An EMP/WDS analysis identified As-rich xenotime-(Y) and a solid solution of wakefieldite–(Ce) and wakefieldite–(Y), which locally enclose individual silicified tracheids. Wakefieldite, identified in silicified plant tissue for the first time, was most likely formed as a secondary mineral during post-depositional diagenesis. The mineral diagenesis did not erase the original anatomy of the wood.
    Print ISSN: 0935-1221
    Electronic ISSN: 1617-4011
    Topics: Geosciences
    Published by Schweizerbart
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  • 10
    Publication Date: 2020-05-06
    Print ISSN: 1439-0108
    Electronic ISSN: 1614-7480
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Published by Springer
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