Abstract
The solid—liquid transition is described by use of the model incorporating the non-linear interactive oscillators. The individual non-linear oscillators are formed from the mechanical units of about the monomer size and produce the vibrations on the lower amplitude level, for the solid phase, either in amorphous or in crystal-like form. As the temperature starts to overpass the Vogel's temperature, the vibrations of individual units are big enough to cause the permanent displacements of the individual vibrating particles; the material starts to flow and the process of diffusion begins as well. As the temperature is passing through T g vicinity, the large mechanical heterogeneity's start to appear as the small percentage of oscillators enlarge their amplitude of vibrations enormously and act as the local stress perturbations centers. These centers are responsible for the destruction of original matrixes and the sharp onset of fluidity and diffusion takes place. The upper amplitude of vibration motion is the basic property of a liquid state. The whole system of vibrations in matrix is described by use of techniques of deterministic chaos theories. It is shown as well, how the mutual interplay of the partition functions (vibration and cohesive), plays the important role in transition from liquid to solid states.
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Hlaváček, B., Šesták, J. & Mareš, J.J. Mutual Interdependence of Partitions Functions in Vicinity T g of Transition. Journal of Thermal Analysis and Calorimetry 67, 239–248 (2002). https://doi.org/10.1023/A:1013770821446
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DOI: https://doi.org/10.1023/A:1013770821446