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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 22 (1995), S. 170-177 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract The compressibility and structural variations of two 2M1 muscovites having compositions (Na0.07K0.90 Ba0.01□0.02)(Al1.84Ti0.04Fe0.07Mg0.04)(Si3.02Al0.98) O10 (OH)2 (7 mole % paragonite) and (Na0.37K0.60□0.03)(Al1.84Ti0.02 Fe0.10Mg0.06)(Si3.03Al0.97) O10(OH)2 (37 mole % paragonite) were determined at pressures between 1 bar and 35 kbar, by single-crystal X-ray diffraction using a Merrill-Bassett diamond anvil cell. Isothermal bulk moduli, setting K′ = 4, were 490 and 540 (± 30) kbar for the Na-poor and Na-rich samples respectively. Both samples show highly anisotropic compressibility patterns, with β a ∶β b ∶β c = 1∶1.15∶3.95 for the Na-poor sample and β a ∶β b ∶β c = 1∶1.19∶3.46 for the Na-rich one. HP structural refinements showed that the different compressibility was largely due to the partial substitution of Na for K in the interlayer region. Moreover, the different compressibility of the tetrahedral and octahedral layers, observed in both micas, increased the a rotation of the tetrahedral layer by about 2° in 28 kbar, as also indicated by the evolution of interlayer cation bond lengths. This increases the repulsion of oxygens of the basal layers and between the high-charged cations of the tetrahedral layer. As a consequence, phengitic substitution, reducing α rotation, would increase the baric stability of mica. Comparison between the HP structures of muscovite and phlogopite indicated the lower compressibility of the latter, mainly due to the greater compressibility of the dioctahedral layer with respect to that of the trioctahedral layer. The HT and HP behaviour of di- and trioctahedral micas showed an anisotropy in the compressional pattern which was markedly greater than that observed in the dilatation pattern. This unexpected result was explained by the different evolution with P and T of alkaliO bond lengths. By combining HP and HT data, a tentative equation of state of muscovite is proposed.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 22 (1995), S. 367-374 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract The thermal behaviour of microsommite (MC), davyne from Vesuvius (DV) and from Zabargad (DZ) was determined by X-ray single crystal data obtained employing a microfurnace connected to a four-circle diffractometer. Upon heating, the a parameter increased linearly, with similar thermal expansion rates for the three samples: the mean linear expansion coefficients, α a , were 10.2(3)·10-6, 13.4(7)·10-6, 15.1(8)·10-1 K-1 for MC, DV and DZ respectively. At about 473 K both MC and DZ showed a discontinuity in the expansion of the c parameter. The mean linear expansion coefficient, α c , changed abruptly from 16(4)·10-6 K-1 for both minerals below the discontinuity to 2(1)·10-6 and 3(1)·10-6 K-1 for MC and DZ, respectively, above the discontinuity. In DV, however, the α c coefficient was constant between 293 und 827 K and equal to 1(2)·10-6 K-1. The substructure of MC was refined under room conditions (R=0.055 with 758 independent reflections) in space group P63 and at 943 K in space group P63 (R=0.062, with 750 independent reflections) and in space group P63/m (R=0.065 with 394 independent reflections). By comparing the structural refinements the discontinuity could be related to the tilting of the tetrahedra connected along c: for T 〈473 K the temperature increase induced the stretching of such chains through tetrahedral tilting. At 473 K the chains were completely stretched and a purely displacive phase transition occured, with symmetry change from space group P6 3 to P63/m. The further limited increase of the c parameter for T〉 473 K was due to the small tetrahedral expansion. In DV, where the completely stretched structure was already realized under room conditions, no phase transition occured.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 24 (1997), S. 274-280 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract  The compressibility and structure of a 2M1 paragonite with composition [Na0.88K0.10Ca0.01Ba0.01] [Al1.97Ti0.007Fe0.01Mn0.002Mg0.006]Si3.01Al0.99O10OH2 were determined at pressures between 1 bar and 41 kbar, by single crystal X-ray diffraction using a Merrill-Bassett diamond anvil cell. Compressibility turned out to be largely anisotropic, linear compressibility coefficients parallel to the unit cell edges being βa=3.5(1)·10−4, βb=3.6(1)·10−4, βc=8.3(3)·10−4 kbar−1 (βa:βb·βc=1:1028:2.371). The isothermal bulk modulus, calculated as the reciprocal of the mean compressibility of the cell volume, was 650(20) kbar. The main features of the deformation mechanism resulting from structural refinements at pressures of 0.5, 25.4, 40.5 kbar were: – variation in sheet thickness, showing that compression of the c parameter was mainly due to the interlayer thickness reduction from 3.07 Å at 0.5 kbar to 2.81 Å at 40.5 kbar; – the compressibility of octahedra was greater than that of tetrahedra, the dimensional misfit between tetrahedral and octahedral sheets increased with P, so that tetrahedral rotation angel α increased from 15° at 0.5 kbar to 21.6° at 40.5 kbar; – the basal surface corrugation (Δz) of the tetrahedral layer, due to the different dimensions of M1 and M2 octahedra and to the octahedral distortion, decreased with P (Δz=0.19 and 0.12 Å at 0.5 and 40.5 kbar respectively). Comparison of the new data on paragonite with those of a K-muscovite and a Na-rich muscovite (Comodi and Zanazzi 1995) revealed a clear trend toward decreasing of compressibility when Na substitutes for K atoms in the interlayer sites.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 18 (1992), S. 483-490 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract The response of magnesiochloritoid to pressure has been studied by single crystal X-ray diffraction in a diamond anvil cell, using crystals with composition Mg1.3Fe0.7Al4Si2O10(OH)4. The unit cell parameters decrease from a = 9.434 (3), b = 5.452 (2), c = 18.136 (5) Å, β = 101.42° (2) (1 bar pressure) to a = 9.370 (7), b = 5.419 (5), c = 17.88 (1) Å, β = 101.5° (1) (42 kbar pressure), following a slightly anisotropic compression pattern (linear compressibilities parallel to unit cell edges: β a = 1.85, β b = 1.74, βc = 3.05 × 10−4 kbar−1) with a bulk modulus of 1480 kbar. Perpendicular to c, the most compressible direction, the crystal structure (space group C2/c) consists of two kinds of alternating octahedral layers connected via isolated SiO4 tetrahedra. With increasing pressure the slightly wavy layer [Mg1.3Fe0.7AlO2(OH)4] tends to flatten. Furthermore, the octahedra in this layer, with all cations underbonded, are more compressible than the octahedra in the (A13O8) layer with slightly overbonded aluminum. Comparison between high-pressure and high-temperature data yields the following equations: $$\begin{gathered} a_{P,T} = 9.434{\text{ }}{\AA} - 174 \cdot 10^{ - 5} {\text{ }}{\AA}{\text{kb}}^{{\text{ - 1}}} \cdot P \hfill \\ {\text{ }} + 9 \cdot 10^{ - 5} {\text{ }}{\AA}^\circ C^{ - 1} \cdot (T - 25^\circ C) \hfill \\ b_{P,T} = 5.452{\text{ }}{\AA} - 95 \cdot 10^{ - 5} {\text{ }}{\AA}{\text{kb}}^{{\text{ - 1}}} \cdot P \hfill \\ {\text{ }} + 5 \cdot 65 \cdot 10^{ - 5} {\text{ }}{\AA}^\circ C^{ - 1} \cdot (T - 25^\circ C) \hfill \\ c_{P,T} = 18.136{\text{ }}{\AA} - 549 \cdot 10^{ - 5} {\text{ }}{\AA}{\text{kb}}^{{\text{ - 1}}} \cdot P \hfill \\ {\text{ }} + 16 \cdot 2^{ - 5} {\text{ }}{\AA}^\circ C^{ - 1} \cdot (T - 25^\circ C) \hfill \\ \end{gathered} $$ with P in kbar and T in °C. These equations indicate that the unit cell and bond geometry of magnesiochloritoid at formation conditions do not differ greatly from those at the outcrop conditions, e.g. the calculated unitcell volume is 917.3 Å3 at P = 16 kbar and T=500 °C, whereas the observed volume at room conditions is 914.4 Å3. In addition, they show that the specific gravity increases from formation at depth to outcrop at surface conditions.
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  • 5
    Publication Date: 2017-04-28
    Print ISSN: 0935-1221
    Electronic ISSN: 1617-4011
    Topics: Geosciences
    Published by Schweizerbart
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  • 6
    Publication Date: 2018-01-01
    Print ISSN: 0935-1221
    Electronic ISSN: 1617-4011
    Topics: Geosciences
    Published by Schweizerbart
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  • 7
    Publication Date: 2020-10-11
    Description: Recent discoveries have demonstrated that the surfaces of Mars, Ceres and other celestial bodies, as well as asteroids and comets, are characterized by the presence of ammonium-bearing minerals. A careful study of remote data compared with the analyses of more accurate laboratory data might allow a better remote characterization of planetary bodies. In this paper, the reflectance spectra of some ammoniated hydrous and anhydrous salts, namely sal-ammoniac NH4Cl, larderellite (NH4)B5O7(OH)2·H2O, mascagnite (NH4)SO4, struvite (NH4)MgPO4·6H2O and tschermigite (NH4)Al(SO4)2·12H2O, were collected at 293 and at 193 K. The aim is to detect how the NH4 vibrational features are affected by the chemical and structural environment. All samples were recovered after cooling cycles and were characterized by X-ray powder diffraction. Reflectance spectra of the studied minerals show absorption features around 1.3, 1.6, 2.06, 2.14, 3.23, 5.8 and 7.27 μm, related to the ammonium group. Between them, the 2ν3 at ~1.56 μm and the ν3 + ν4 at ~2.13 μm are the most affected modes by crystal structure type, with their position being strictly related to both anionic group and the strength of the hydrogen bonds. The reflectance spectra of water-rich samples [struvite (NH4)MgPO4·6(H2O) and tschermigite (NH4)Al(SO4)2·12(H2O)] show only H2O fundamental absorption features in the area from 2 to 2.8 μm and a band from hygroscopic water at 3 μm. Thermal analyses (TA), thermal gravimetry (TG) and differential scanning calorimetry (DSC) allowed to evaluate the dehydration temperatures and the occurring phase transitions and decompositions in the analyzed samples. In almost all samples, endothermic peaks at distinct temperatures were registered associated to loss of water molecules, differently linked to the structures. Moreover, an endothermic peak at 465 K in sal-ammoniac was associated to the phase transition from CsCl to NaCl structure type.
    Electronic ISSN: 2075-163X
    Topics: Geosciences
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  • 8
    Publication Date: 1988-01-01
    Print ISSN: 0375-6505
    Electronic ISSN: 1879-3576
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Published by Elsevier
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  • 9
    Publication Date: 1988-01-01
    Print ISSN: 0375-6505
    Electronic ISSN: 1879-3576
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Published by Elsevier
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  • 10
    Publication Date: 2019-04-18
    Description: High-pressure single-crystal synchrotron X-ray diffraction data for galenobismutite, PbBi2S4 collected up to 20.9 GPa, were fitted by a third-order Birch-Murnaghan equation of state, as suggested by a FE-fE plot, yielding V0 = 697.4(8) Å3, K0 = 51(1) GPa and K’ = 5.0(2). The axial moduli were M0a = 115(7) GPa and Ma’ = 28(2) for the a axis, M0b = 162(3) GPa and Mb’ = 8(3) for the b axis, M0c = 142(8) GPa and Mc’ = 26(2) for the c axis, with refined values of a0, b0, c0 equal to 11.791(7) Å, 14.540(6) Å 4.076(3) Å, respectively, and a ratio equal to M0a:M0b:M0c = 1.55:1:1.79. The main structural changes on compression were the M2 and M3 (occupied by Bi, Pb) movements toward the centers of their respective trigonal prism bodies and M3 changes towards CN8. The M1 site, occupied solely by Bi, regularizes the octahedral form with CN6. The eccentricities of all cation sites decreased with compression testifying for a decrease in stereochemical expression of lone electron pairs. Galenobismutite is isostructural with calcium ferrite CaFe2O4, the suggested high pressure structure can host Na and Al in the lower mantle. The study indicates that pressure enables the incorporation of other elements in this structure, increasing its potential significance for mantle mineralogy.
    Electronic ISSN: 2073-4352
    Topics: Physics
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