Abstract:
Low-frequency IR-spectra of glassy polymers were obtained and analyzed at temperatures from 90 to 400 K. Temperature changes in the
IR-spectra in the range from 10 to 140 cm$^{-1}$ show three universal features: low-temperature, corresponding to the torsional-vibrational motion of monomer units, high-temperature, due to the influence of primary relaxation (glass transition) and intermediate, caused by the activation of conformational mobility in chains at a temperature of $\beta$-transition. This versatility extends both to polymers with universal chain-to-chain interactions and to those with hydrogen bonds.
Keywords:IR spectra, excess density of vibrational states, bosonic peak, molecular dynamics, $\alpha$- and $\beta$-relaxations.