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  • Physics  (1)
  • active solids  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 38 (1992), S. 111-130 
    ISSN: 1572-8943
    Keywords: active solids ; kinetic ; thermodynamic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die Herstellung eines aktiven Feststoffes durch thermische Zersetzung einiger Präkursorsubstanzen, meistens eines Oxysalzes, ist nur der eine Weg zur Herstellung solcher Substanzen. Die Aktivität der Feststoffe besteht an ihrer Oberfläche, obwohl sich ein Teil der Oberfläche auch im Innern oder bei Zersetzungsprozessen an der Reaktionsgrenzfläche befinden kann. Die eigentümliche Eigenschaft einiger Feststoffphasen besteht darin, da\ man, um sie richtig beschreiben zu können, die Vorgeschichte der Substanz berücksichtigen mu\ und es kann gezeigt werden, da\ die Vorgeschichte einer Substanz hauptsächlich die der Veränderung der Oberflache und der Feinstruktur ist. Diese Tatsache beeinflu\t die Anwendung von Thermodynamik und Reaktionskinetik bei Prozessen mit Feststoffen. Dies ist besonders bei aktiven Feststoffen offensichtlich, bei denen an oder in der Nähe der Oberfläche verhältnismä\ig mehr chemische Stoffe vorkommen als üblicherweise. Dies wird durch die Existenz von vielen oder mehreren aktiven Feststoffen in einer amorphen Phase und durch die mögliche Koexistenz verschiedenartiger Festphasen bezeugt. In vorliegendem überblick wird die Nützlichkeit der Strukturbestimmung normaler Feststoffphasen sowie die Art der möglichen Anwendung der Thermoanalyse bei der Bestimmung thermodynamischer und kinetischer Parameter diskutiert.
    Notes: Abstract The production of an active solid by thermal decomposition of some precursor material usually an oxysalt is only one way of producing such a material. The activity of any solid resides at the surface albeit some of the surface may be internal or in the decomposition process a reaction interface. The peculiar property of any solid phase is that to describe it properly one must cite the pre-history of the material, and it can be shown that the pre-history of any solid phase is mainly that of altering the surface and textural properties. This fact influences the application of thermodynamic and kinetics to processes involving the solid phase. This becomes more evident in the case of active solids where a larger proportion of chemical species than usual resides at or near the surface. This is evidenced by the existence of many or more active solids in an amorphous phase and the possible co-existence of different types of solid phase. In this review, the usefulness of normal solid phase structural determination is discussed and the manner in which thermal analysis can be used to determine thermodynamic and kinetic parameters.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1703-1711 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal degradation of four different forms of cellulose in nitrogen has been studied by using a thermobalance. In TG experiments a total weight loss at 900°C was 80% in the cases of film and pulp samples and 83% for two powder forms. The results for the isothermal degradation of the four samples at 270°C are plotted as degree of degradation α against reduced time t/t0.5 and compared with the master plots of Sharp, Brindley, and Achar. The experimental data fit most closely the plot for the Avrami-Erofeev equation in the form kt = {-ln (1-α)}1/n where n = 2. An activation energy of 144 kJ/mole has been found for the degradation of one of the celluloses from the results of isothermal runs at six different temperatures. It is postulated here that the thermal degradation occurs by random nucleation and nucleus growth in the cellulose fibrils so as to yield a carbon whose microporous structure is a replica of the pore system in the parent cellulose.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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