Transition molecular structures between block copolymers and hyperbranched copolymers suitable for toughening epoxy thermosets

Various toughening agents had been explored to overcome the intrinsic brittleness of epoxy thermosets. While they effectively toughened epoxy thermosets, however, usually produced plasticizing effect, leading to compromised thermal stability, modulus and glass transition temperature (T-g). Herein dumbbell-shaped SEBS-g-PEG copolymers, owning transitional molecular structures between block copolymers and hyperbranched copolymers, were synthesized via grafting methoxypolyethylene glycol (PEG) onto both end blocks of polystyrene-b-poly(ethylene-ran-butylene)-b-polystyrene (SEBS). They not only had good compatibility with epoxy thermosets without plasticizing effect, but also could form micro-phase separation morphology suitable for toughening epoxy thermosets via combining the advantages of block copolymers and hyperbranched copolymers. At higher branching density, their 10% load could increase similar to 230% K-IC and impact strength without sacrificing thermal stability, T-g, flexural strength and modulus. The morphology results showed that their soft nanostructures' size increased and the phase interfaces became blurred as increasing the branching density in SEBS-g-PEG. Thus, the toughening mechanism was attributed to the strengthened bonding between the interphases and the enlarged size of soft nanostructures.

Automated summary

In this study, SEBS-g-PEG copolymers with transitional molecular structures were synthesized to toughen epoxy thermosets. These copolymers showed good compatibility with epoxy thermosets without plasticizing effect and could form micro-phase separation morphology suitable for toughening the epoxy thermosets. Increasing branching density in SEBS-g-PEG improved toughening effect while maintaining thermal stability of the materials.