Radical-Mediated Ring-Opening Photopolymerization for Semicrystalline Thermoplastic Additive Manufacturing
Alex J. Commisso, Gopal R. Sama, Timothy F. Scott
Abstract
Conventional approaches to stereolithographic additive manufacturing (SLA) employ liquid resin formulations based on multifunctional (meth)acrylates and epoxides that afford cross-linked polymeric networks upon polymerization. Nevertheless, the utilization of resins that yield semicrystalline thermoplastics provides facile access to physical and mechanical properties that are otherwise difficult to attain, such as high toughness and resistance to solvent swelling as well as additional postfabrication processing options that can be used to extend the life cycle of three-dimensional printed polymers. Here, we report the SLA-based additive manufacturing of semicrystalline thermoplastics utilizing the radical-mediated ring-opening photopolymerization of seven- and eight-membered cyclic allylic sulfides. Photopolymerization of resin formulations incorporating seven- and eight-membered cyclic allylic sulfides and crystallization of the resultant (co)polymers were examined using Fourier transform infrared spectroscopy, photorheology, and isothermal photo-differential scanning calorimetry. The formulated resins were found to polymerize and subsequently crystallize rapidly upon irradiation under ambient conditions. The mechanical properties of stereolithographically printed copolymers approached the bulk copolymer mechanical properties, demonstrating unusually strong interlayer adhesion atypical of layerwise, stereolithographic printing of semicrystalline polymers. Finally, high-quality, recyclable, semicrystalline thermoplastic parts were printed and melted down, demonstrating the potential for these semicrystalline materials to provide a path for improved sustainability of polymeric parts produced via SLA.