Abstract
The laws of internal mass transfer under deep drying of granular polymers depending on their state have been considered. From the point of view of the system approach, the general problem of their drying kinetics has been decomposed into two basic levels: a micro- and a macroscopic one, and, in accordance with this, the questions of mathematical modeling have been analyzed. The experimental data on the diffusion and sorption properties and longitudinal mixing of the solid phase are presented and recommendations on the apparatus arrangement of the process are given.
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