Source abstract
Abstract
Relative to other additive manufacturing modalities, vat photopolymerization (VP) offers designers superior surface finish, feature resolution, and throughput. However, poor interlayer network formation can limit a VP-printed part’s tensile strength along the build axis. We demonstrate that the incorporation of carbamate bonds capable of undergoing dissociative exchange reactions provides improved interlayer network formation in VP-printed urethane acrylate polymers. In the presence of dibutyltin dilaurate catalyst, the exchange of these carbamate bonds enables rapid stress relaxation with an activation energy of 133 kJ/mol, consistent with a dissociative bond exchange process. Annealed XY tensile samples containing a catalyst demonstrate a 25% decrease in Young’s modulus, attributed to statistical changes in network topology, while samples without a catalyst show no observable effect. Annealed ZX tensile samples printed with layers perpendicular to tensile load demonstrate an increase in elongation at break, indicative of self-healing. The strain at break for samples containing a catalyst increases from 33.9 to 56.0% after annealing but decreases from 48.1 to 32.1% after annealing in samples without a catalyst. This thermally activated bond exchange process improves the performance of VP-printed materials via self-healing across layers and provides a means to change Young’s modulus after printing. Thus, the incorporation of carbamate bonds and appropriate catalysts in the VP-printing process provides a robust platform for enhancing material properties and performance.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States
Department of Chemistry and Biochemistry, California Polytechnic State University, San Luis Obispo, California 93407, United States
Department of Mechanical Engineering, Macromolecules Innovation Institute, Virginia Tech, Blacksburg, Virginia 24061, United States
Department of Chemistry, Macromolecules Innovation Institute, Virginia Tech, Blacksburg, Virginia 24061, United States
Department of Chemistry and Chemical Biology, Cornell University, Baker Laboratory, Ithaca, New York 14853, United States
School of Molecular Sciences, Biodesign Center for Sustainable Macromolecular Materials and Manufacturing, Arizona State University, Tempe, Arizona 85281, United States
Funding
Honeywell Federal Manufacturing and Technologies · National Science Foundation