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Highly Reprocessable Diels-Alder Networks with Rapid Gelation for Enhanced Printability
George Misiakos1, Sandra Van Vlierberghe1
1Polymer Chemistry and Biomaterials Research Group (PBM), Centre of Macromolecular Chemistry (CMaC), Department of Organic and Macromolecular Chemistry, Faculty of Sciences, Ghent University, Krijgslaan 281 Building S4, Ghent 9000, Belgium.
None:
Extrusion-based additive manufacturing of dynamic covalent polymer networks has faced longstanding challenges, preventing widespread adoption. Dynamic cross-linking via the thermoreversible Diels-Alder (DA) reaction has shown potential, however slow reaction rates resulting in poor viscosity control and thermal instability have posed significant constraints. Herein, we present a modular, scalable, solvent-free synthetic approach tailored to extrusion-based 3D printing. Linear oligomers densely functionalized with furan pendant groups are synthesized to accelerate postextrusion gelation. Through facile control of cross-linking density, networks with stiffnesses spanning from 2 to 200 MPa are obtained. Exceptional robustness to processing conditions is demonstrated via dynamic rheology, with networks undergoing 20 reprocessing cycles, marking a significant improvement for DA-based materials. Autonomous scratch healing at 20 °C is shown by a network combining high cross-linking density and chain mobility. Structures with mm-thin upright walls were printed using minimal or no support, marking an advancement in achievable features using purely dissociative DA-cross-linked networks, without viscosity-regulating additives. Fast gelation unlocks the trade-off between solidification rates and interlayer cross-linking, facilitating shape retention while mitigating mechanical anisotropy. The proposed approach establishes a pathway toward the scalable production of recyclable, tunable dynamic networks, providing a versatile platform for additive manufacturing, self-healing applications, and sustainable material development.
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