LAUSR

Abstract 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.