Understanding the Topology Freezing Temperature of Vitrimer-Like Materials through Complementary Structural and Rheological Analyses for Phase-Separated Network.

Vitrimers are sustainable cross-linked polymers characterized by an associative bond exchange mechanism within their network. A well-known feature of vitrimers is the Arrhenius dependence of the viscosity or relaxation time. Another important aspect is the existence of a topology-freezing temperature (), which represents a transition between the viscoelastic solid state and the malleable viscoelastic liquid state. Various methods, including viscosity-temperature plots and temperature-ramp creep (or dilatometry), have been proposed for determining the . In this study, we complementarily employ X-ray scattering-based structural analysis and rheological analysis to assign in phase-separated vitrimer-like materials undergoing trans--alkylation bond exchange. Note that the --alkylation progresses via the dissociative bond exchange pathway, whereas our previous studies demonstrated that the temperature-dependence of relaxation time followed the Arrhenius dependence, which was the reason for the classification as a vitrimer-like material. Specifically, we identify as the temperature at which an anomalous increase in domain distance occurs during the rubbery state in the structural analysis. In the rheological analysis, corresponds to the transition temperature marking the shift from the Williams-Landel-Ferry dependence to the Arrhenius dependence in the shift factors used to create master curves for frequency sweep rheology data. Importantly, both methods yield nearly the same , validating the accuracy of the proposed assignment and, thus, providing valuable insights into the specific properties of vitrimers.