“…However, in many cases, e. g., near glass transition temperatures and mechanical relaxations of polymers, the use of traditional methods of experimental results processing for thermal activation spectroscopy leads to abnormally high values of activation energy of E a electrically active defects (EAD) participating in the relaxation process and unrealistic relaxation time values less than 10 −20 seconds (Shabanova, Temnov 2021). This is due to the fact that in this case the relaxation process involves the cooperative movement of molecular chain segments, and the precise determination of the activation energy of one relaxer requires taking into account the change in the free volume of the polymer during the relaxation transition.…”