Cationic photopolymerization of cyclic esters at elevated temperatures and their application in hot lithography

Abstract

AbstractThe 3D printing of polyesters is most commonly performed using polylactide filaments for material extrusion (formerly known as fused‐deposition modelling) or by introducing methacrylate end‐groups to polyesters, which can be polymerized by a radical mechanism. However, cyclic esters can also be polymerized via cationic ring‐opening photopolymerization, which opens up the possibility of using high‐resolution stereolithography as the method of choice to form polyester networks in situ during the printing process. Hereby, we present the first approach to 3D print polyesters starting directly from ε‐caprolactone via stereolithography at elevated temperatures, by introducing low amounts of crosslinks into the material to provide stability to the structure but maintain its degradable character and especially semicrystallinity. Photorheology tests showed that high temperatures and the introduction of crosslinkers led to increased reactivity and fast gelation. By performing tensile tests, dynamic mechanical thermal analysis and simultaneous thermal analysis the material properties were evaluated depending on the amount and type of crosslinker. It was shown that decreasing the amount of crosslinker significantly increased the crystallinity and influenced the mechanical properties as well as shape memory properties. Finally, successful 3D printing of a polyester was performed using 10 mol% of a crosslinker with oxetane moieties and 90 mol% ε‐caprolactone at 120 °C. © 2022 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry.