Three crosslinked polyurethane copolymers were successfully synthesized as polymeric solid–solid phase change materials (SSPCMs) for thermal energy storage. These materials were fabricated utilizing trihydroxy compounds (glycerol, triethanolamine, and trimethylolethane) as chain extenders and polyethylene glycol (PEG) as the phase change functional segment. A comprehensive suite of characterization techniques was employed to investigate the chemical structures, thermal properties, and crystalline behaviors of the resulting SSPCMs. Fourier transform infrared (FTIR) spectroscopy confirmed the successful synthesis of the crosslinked polyurethane network. Polarizing optical microscopy (POM) and wide-angle X-ray diffraction (WAXD) analyses revealed that all three SSPCMs exhibit regular spherulitic morphologies with sharp diffraction peaks resembling those of pure PEG, although variations in spherulite size and diffraction intensity were observed among the samples. Differential scanning calorimetry (DSC) demonstrated the reversible latent heat storage and release capabilities of the synthesized SSPCMs, with a maximum endothermic enthalpy (ΔHendo) of 115.7 J/g. Furthermore, thermal cycling tests and thermogravimetric (TG) analysis verified their exhibit excellent reusability, thermal reliability, and high thermal stability.
Zhang et al. (2026) studied this question.