This study aims to present a design and investigation of novel vanillin-based thiol-ene photocurable systems as candidate materials for optical three-dimensional printing.
Two vanillin acrylates, vanillin dimethacrylate and vanillin diacrylate, were tested in thiol-ene photocurable systems with 1,3-benzenedithiol. The kinetics of photocross-linking was investigated by real-time photorheometry using two photoinitiators, diphenyl (2,4,6-trimethylbenzoyl)phosphine oxide or ethyl (2,4,6-trimethylbenzoyl)phenylphosphinate in different quantities. The dependencies of rheological properties of resins on the used vanillin derivative, photoinitiator, and the presence of a solvent, as well as structure, thermal and mechanical properties of the selected polymers were investigated.
The most rigid polymers were obtained from vanillin diacrylate-based resins without any solvent. The vanillin diacrylate-based polymer possessed higher values of cross-linking density, the yield of insoluble fraction, thermal stability and better mechanical properties in comparison to the vanillin dimethacrylate-based polymer.
The kinetics of photocross-linking of vanillin-based thiol-ene systems was investigated by real-time photorheometry for the first time. The designed novel photocurable systems based on vanillin acrylates and 1,3-benzenedithiol are promising renewable photoresins for optical three-dimensional printing on demand.
