Confined crystallization and degradation of six-arm star PCL with core of cyclotriphosphazene in epoxy thermosets

Six-arm star polycaprolactone with core of cyclotriphosphazene ( s -PCL) was synthesized via ring-opening polymerization and characterized by NMR and GPC . Epoxy thermosets incorporating 10–40  wt % of this copolymer were cured with 4,4′-methylenebis(2-chloroaniline) (MOCA) and 4,4′-diaminodiphenyl sulfone (DDS), respectively. In these thermosets, intermolecular specific interactions had a significant impact on their morphologies. Specifically, no discernable macroscopic phase separation was found in FESEM images of MOCA-cured epoxy resins . However, for the DDS-cured system, s -PCL was partially miscible with the epoxy thermosets, as evidenced with FTIR and DMA. This is may be owning to enriched concentration of hydroxyl groups in the s -PCL favored the miscibility between PCL subchains of carbonyl and the epoxy matrix. Dispersed phase, further confirmed by XRD to be amorphous , with a diameter of 0.34–0.44 μm could be observed ( s -PCL’ content ≤ 20  wt %) in this system. Nevertheless, crystallization of PCL could not be suppressed completely ( s -PCL’ content > 30  wt %). Besides, epoxy thermosets containing crystalline PCL were found to be more resistant to thermal degradation but sensitive to alkaline degradation (10% NaOH aqueous solution) according to TGA and FESEM results. This work presented here is a meaningful report on the presence of alkaline-labile crosslinking points through the whole networks.