Heat capacity, viscosity, and configurational entropy of alkali titanosilicate melts

Details Heat capacity, viscosity, and configurational entropy of alkali titanosilicate melts Heat capacity, viscosity, and configurational entropy of alkali titanosilicate melts

Aug 1999

adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1999gecoa..63.2429a&link_type=abstract

Geochimica et Cosmochimica Acta, vol. 63, Issue 16, pp.2429-2437

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The heat capacities of three sodium and potassium titanosilicate glasses and melts have been determined between room temperature and 1800 K. For all melts, the heat capacity decreases with increasing temperatures after a 30% to 53% rise at the glass transition. For both glasses and melts, the heat capacity is an additive function of composition, which indicates that the calorimetric anomalies are an intrinsic feature of the TiO 2 component that depends neither on the relative abundances of SiO 2 and Na 2 O or K 2 O, nor on the nature of the alkali cation. The viscosities measured for these and two other melts indicate that, as embodied by the Adam-Gibbs theory of relaxation processes, the considerable decrease of the melt configurational entropy results in a dramatic viscosity increase near the glass transition range. Consistent with the major influence of configurational entropy, structural relaxation in the glass transition range proceeds much more slowly for Ti-bearing than for Ti-free melts. These various features are attributed to important temperature-induced changes in short-range order around oxygen atoms, with strongly decreasing substitution of Ti for Si at lower temperatures constituting probably the main factor.

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