SynopsisThe results of the experimental and molecular-dynamics study of the process of mechanical degradation of polymer chain, testifying to the essential role of nonthermal channels of dissipation of elastic energy accumulated during deformation, have been discussed. High-energy molecular products of mechanical degradation, which are able to induce a chain branching process leading to "explosive" formation of submicrocracks, have been discovered. It has been noted that a considerable part of polymer chain energy is concentrated in localized excitations of a soliton type, which play the determining role at all the stages of mechanical degradation under consideration.Deformation and fracture of polymers as well as of other solids are accompanied by complex and little-studied physicochemical processes. One may assume that, a t the stage going immediately after the first act of macromolecule breaking, the elastic energy stored in the macromolecule during its stretching dissipates in the following way:-It leads to electronic excitation and ionization and is carried away by electrons, photons, and ions. -It is spent on the fragmentation of chains and transforms into translational, rotatory, and vibratory energy of molecular products of mechanical degradation.--It transforms into heat including infrared (IR) radiation.Ultimately, the energy of molecular products of mechanical degradation, electrons, ions, and photons also transforms into heat. This may lead to additional IR radiation, thermal degradation, and plastic flow.Theoretical interpretation of mechanical degradation is based on a model of thermal fluctuations,' which takes into account only thermal processes. These characteristic times of elastic energy thermalization are practically assumed to be small so that direct influence of nonthermal effects on mechanical degradation can be neglected. Both experimental data and the results of computer simulation of mechanical degradation of polymer chain by the method of molecular dynamics are discussed in terms of thermal fluctuations.2 At the present time the consistent molecular theory of mechanical degradation has not been available.Two principal questions arise in connection with the development of such a theory. Speaking about thermal fluctuations in solids, one usually bears in mind phonons, which are determined in a harmonic approximation and