THERMOPHYSICAL ASPECTS OF POLYMER CRYSTALLIZATION AND THEIR RELATION TO THE DIPOLE CHARACTERISTICS OF MACROMOLECULES
Abstract and keywords
Abstract:
The study is devoted to establishing a relationship between the thermophysical conditions of the crystallization of linear polymers and the change in their molecular dipole characteristics. The relevance of the work is due to the need to understand the mechanisms of structure formation in polymer materials used in elements of thermal power equipment. Based on a conformational approach and modeling of the internal electric field that arises in a non-uniform temperature field, an analytical expression is obtained that relates the average square of the dipole moment of a macromolecule to its molar mass. Numerical calculations have been performed for a number of polymethylsiloxane liquids (PMS) in the phase transition interval. It has been shown that the dependence of the average dipole moment square on the molar mass has a non-monotonic character with extrema that correspond to the change of crystallization mechanisms. Critical values of molar mass (about 3000 kg/mol) have been determined, at which the transition from crystallization with extended chains to crystallization with folded chains occurs, which directly affects the thermophysical properties of the material, such as thermal conductivity and the temperature coefficient of linear expansion.

Keywords:
polymer crystallization, thermophysical properties, dipole moment, polymethylsiloxane, molar mass, non-uniform temperature field, phase transition
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