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  • 1
    Publication Date: 2019-07-16
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , notRev
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 23 (1958), S. 477-478 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 57 (1953), S. 382-384 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 24 (1959), S. 1025-1026 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0020-711X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Mineralogy and petrology 66 (1999), S. 271-299 
    ISSN: 1438-1168
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung In dieser Studie werden die thermodynamischen Eigenschaften der Granate im System (Fe2+,Mn2+, Mg, Ca)3Al2Si3O12 kritisch zusammengestellt. Die thermodynamischen Eigenschaften der drei Endglied-Granate Pyrop, Almandin und Grossular, einschließlich ihrer Volumina, Bildungswärmen, Entropien, Kompressibilitäten und thermischen Ausdehnungen wurden bereits hinreichend gut bestimmt. Dagegen müssen die Bildungswärme und Tieftemperatur-Wärmekapazität von Spessartin noch gemessen werden. Die Eigenschaften des Pyrops sind wahrscheinlich mit den großen anisotropen Schwingungen des kleinen, leichten Mg-Kations verbunden. Die thermodynamischen Mischungseigenschaften der sechs binären Mischkristallreihen werden ebenfalls diskutiert. Während die Mischungs-Volumendaten der binären Mischreihen gut bekannt sind, müssen ihre Mischungs-Enthalpien und Standard-Mischungsentropien noch ermittelt werden. Es wurde gezeigt, daß die Größe der positiven Exzeß-Volumina mit dem Volumen-Unterschied der zwei Endglied-Komponenten der jeweiligen Mischreihe verknüpft ist. Es ist wahrscheinlich, daß Exzeß-Entropien, wenn vorhanden, erst bei Tieftemperaturen unter 200 K auftreten. Neue29Si NMR-Experimente belegen, daß in Pyrop-Grossular-Mischkristallen Nahordnung von Mg und Ca vorliegt. Der Effekt der Nahordnung muß in künftigen thermodynamischen Modellen berücksichtigt werden. Hieraus ergibt sich die Notwendigkeit, alle Granat-Mischreihen auf mögliche Nahordnung hin zu untersuchen. Die Mischungseigenschaften der Pyrop-Grossular-Mischreihe, die von sämtlichen Granat-Mischreihen am besten bestimmt wurden, können teilweise mit dem Quasi-Chemical-Model beschrieben werden. Dieses Modell ermöglicht die Beschreibung der mikroskopischen Wechselwirkungen, die die makroskopischen thermodynamischen Eigenschaften bestimmen. Mikroskopische Eigenschaften werden am besten mit spektroskopischen Messungen und theoretischen Berechnungen untersucht. Hard-mode IR-Spektroskopie-Messungen an binären Mischreihen zeigen, daß die lokalen mikroskopischen strukturellen Verzerrungen in den makroskopischen Mischungs-Volumina widergespiegelt werden. Die Art der Spannungsfelder und Platz-Relaxationen muß detaillierter untersucht werden, um ein besseres Verständnis des Mischkristall-Bildungsprozsses und der Energetik der Granate zu erreichen. Darüber hinaus werden wichtige künftige Forschungsgebiete diskutiert.
    Notes: Summary The thermodynamic properties of garnets in the system (Fe2+, Mn2+, Mg, Ca)3A12Si3O12 are reviewed. The thermodynamic properties of the three end-member garnets pyrope, almandine and grossular, including their volume, enthalpy of formation, entropy, compressibility and thermal expansion have been well determined. For spessartine enthalpy of formation and heat capacity at low temperatures are needed. Pyrope's unusual behavior in some of its properties is probably related to the presence of the small, light Mg cation, which has a large anisotropic thermal vibration. The thermodynamic mixing properties of the six binaries are also discussed. Good volume of mixing data exist now for all of the binaries, but much work is still required to determine the enthalpies and third-law vibrational entropies of mixing. It is shown that the magnitude of the positive deviations in the volumes of mixing is related to the volume difference between the two end-member components. It is probable that excess entropies, if present, originate at low temperatures below 200 K. Recent29Si NMR experiments have demonstrated the presence of short-range ordering (SRO) of Ca and Mg in pyrope-grossular solid solutions. Short-range order will have to be considered in new models describing the entropies of mixing. Its possible presence in all garnet solid solutions needs to be examined. The mixing properties of pyrope-grossular garnets, which are the best known for any garnet binary, can, in part, be described by the Quasi-Chemical approximation, which gives insight into the microscopic interactions which determine the macroscopic thermodynamic mixing properties. Microscopic properties are best investigated by spectroscopic and computational approaches. Hard mode IR measurements on binary solid solutions show that the range of local microscopic structural distortion is reflected in the macroscopic volumes of mixing. The nature of The contents of this contribution was presented at the IMA Meeting in Toronto in August, 1998. It precedes issues of “Mineralogy and Petrology” containing thematic sets of IMApapers strain tiields and site relaxation needs to be studied in order to obtain a better understanding of the solid-solution process and energetics in garnet. Critical areas for future experimentation are also addressed.[/p]
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 138 (2000), S. 46-50 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The heat capacity of synthetic anhydrous Mg and Fe cordierite was measured by differential scanning calorimetry (DSC). Mg cordierite was synthesized from a glass at high temperatures and shows an ordered structural state. Fe cordierite was synthesized hydrothermally and dehydrated under reducing conditions to obtain H2O-free material. IR spectroscopy was used to ascertain the lack of H2O in both phases. The molar volume of both phases was measured using powder X-ray diffraction giving 23.316 (7) J/bar for Mg cordierite and 23.672 (6) J/bar for Fe cordierite. DSC measurements between 300 and 950 K were made following the procedure of Bosenick et al. (1996). The data show a precision of about 1% in the case of Mg cordierite and 1.5% for Fe cordierite. Fitted Cp polynomials in J/mol/K are: and for Mg and Fe cordierite, respectively. The Cp values determined for Mg cordierite are slightly larger (1–3%) than those measured by drop calorimetry by Pankratz and Kelley (1963). The Cp data for Fe cordierite permit the calculation of its standard third-law entropy, So 298 K from the reaction 3Fe cordierite=2 almandine + 4 sillimanite + 5 quartz giving 465 J/mol/K, which is in good agreement with recent model estimates.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 25 (1998), S. 142-151 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract  The single-crystal polarized Raman spectra of four natural silicate garnets with compositions close to end-members almandine, grossular, andradite, and uvarovite, and two synthetic end-members spessartine and pyrope, were measured, along with the powder spectra of synthetic pyrope-grossular and almandine-spessartine solid solutions. Mode assignments were made based on a comparison of the different end-member garnet spectra and, in the case of pyrope, based on measurements made on additional crystals synthesized with 26Mg. A general order of mode frequencies, i.e. R(SiO4)〉T(metal cation)〉T(SiO4), is observed, which should also hold for most orthosilicates. The main factors controlling the changes in mode frequencies as a function of composition are intracrystalline pressure (i.e. oxygen-oxygen repulsion) for the internal SiO4-vibrational modes and kinematic coupling of vibrations for the external modes. Low frequency vibrations of the X-site cations reflect their weak bonding and dynamic disorder in the large dodecahedral site, especially in the case of pyrope. Two mode behavior is observed for X-site cation vibrations along the pyrope-grossular binary, but not along the almandine-spessartine join.
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  • 10
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Synthetic almandine garnet, Fe3Al2Si3O12, has been studied by temperature — dependent single crystal X-ray diffraction and57Fe Mössbauer spectroscopy. The Fe2+ doublet in almandine is characterized by a small asymmetry between the high and low-velocity peaks that decreases in magnitude with decreasing temperature from 420 to 15 K. The X-ray results show that the Fe2+ cation is dynamically disordered with an anisotropic motion within the eight-coordinated site in garnet. The magnitudes of the X-ray determined mean-square-vibrational amplitudes of this motion parallel,x ∥, and perpendicular,x ⊥, to the principle axes of the electric field gradient give a calculated angular dependence of the electric quadrupole interaction of theI 1/2 toI 3/2 transitions that agree with the experimentally measured peak ratios. This is the first recognition of anisotropic recoil free fraction of57Fe in silicates.
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