The dielectric spectra
of the poly(thiourethane) network,
HDI-S3,
have been analyzed to know the nature and the cooperativity of each
of the six dielectric processes observed. At low temperatures, γ1, γ2, and β dielectric relaxations
were attributed to noncooperative local motions in the glassy state,
in which apparent activation energies are 30, 36, and 60 kJ·mol–1, respectively. At higher temperatures, three dielectric
relaxations are observed (αTg, α*, ρ).
The αTg relaxation is attributed to the glass transition,
and it is overlapped with the α* relaxation. The molecular origin
of α* relaxation is associated with the bond exchange reaction.
Finally, the ρ relaxation is ascribed to the heterogeneity of
the sample although its origin is uncertain. The DC conductivity (σDC) is found to be an appropriate variable to analyze the bond
exchange reaction. Accordingly, the HDI-S3 has a molecular exchange
mechanism of dissociative nature.