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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 52 (1998), S. 5-16 
    ISSN: 1572-8943
    Keywords: calcite ; kinetic ; phase transition ; thermal activation ; transition enthalpy ; vaterite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The vaterite—calcite transition above 630 K has been studied by isothermal and non-isothermal differential scanning calorimetry. Vaterite samples prepared under different conditions were investigated. The transition temperature is strongly dependent on the sample preparation. The observed transition enthalpy ΔHtr is nearly equal for different samples and experimental conditions. From 28 measurements a value of ΔHtr−(3.12±0.11) kJ mol−1 was obtained. The activation energy for the polymorphic transition was calculated from the Arrhenius plot and by use of isoconversional methods, as a function of the degree of conversion. The influence of the kinetic model distortion and experimental uncertainties on the obtained data was discussed. The actual value of the activation energy was assessed at Ea=(250±10) kJ mol−1 for nearly all examined samples. Functions, corresponded to the model mechanism of nuclei formation and growth, provide the unambiguous consideration of the transition kinetic for the investigated vaterite samples. Differences in the dynamic behaviour of several samples at the transition are established.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 60 (2000), S. 463-472 
    ISSN: 1572-8943
    Keywords: calcite ; calcium carbonate polymorphs ; phase transition ; thermodynamics ; vaterite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Although vaterite is the least stable anhydrous calcium carbonate polymorph, it is formed as a metastable phase in some normal and pathological biomineralisation processes. In this work, thermodynamic aspects of the vaterite-calcite phase transition were comprehensively studied. Vaterite samples were prepared by different methods and characterised for the composition, crystal structure, specific surface and grain size. All products were identified to be pure vaterite by careful X-ray diffraction measurements. The enthalpy and Gibbs energy of transition were determined by precise calorimetric and potentiometric measurements. The reliability of the thermodynamic data for the vaterite-calcite phase transition derived from this work was shown by the use of different calorimetric methods to determine the enthalpy of transition and the independent measurements of heat capacity and entropy of vaterite. Our recommended values are Δtrs G*=−2.9±0.2 kJ mol−1 , Δ trs H *=−3.4±0.2 kJ mol−1 and Δ trs S *=−1.7±0.9 J K−1 mol−1 , where the uncertainties are given as twice the standard deviations.
    Type of Medium: Electronic Resource
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