Volumetric Additive Manufacturing of Dicyclopentadiene by Solid‐State Photopolymerization
Source abstract
Abstract
Abstract Polymerization in the solid state is generally infeasible due to restrictions on mobility. However, in this work, the solid‐state photopolymerization of crystalline dicyclopentadiene is demonstrated via photoinitiated ring‐opening metathesis polymerization. The source of mobility in the solid state is attributed to the plastic crystal nature of dicyclopentadiene, which yields local short‐range mobility due to orientational degrees of freedom. Polymerization in the solid state enables photopatterning, volumetric additive manufacturing of free‐standing structures, and fabrication with embedded components. Solid‐state photopolymerization of dicyclopentadiene offers a new paradigm for advanced and freeform fabrication of high‐performance thermosets.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Synthetic Organic Chemistry Methods · Photopolymerization techniques and applications · Advanced Polymer Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemical Engineering and Materials Science University of Minnesota Minneapolis MN 55455 USA
Sandia National Laboratories Albuquerque NM 87185 USA
Funding
U.S. Department of Energy · Office of Science
References (29)
Show source-provided references
1. 10.1021/ar800142710.1021/ar8001427 ↗
2. 10.1039/D0CS00840K10.1039/D0CS00840K ↗
3. 10.1021/ma802406j10.1021/ma802406j ↗
4. 10.1039/C2NJ40557A10.1039/C2NJ40557A ↗
5. 10.1016/B978-0-08-096701-1.00132-410.1016/B978-0-08-096701-1.00132-4 ↗
6. 10.1016/j.jphotochem.2023.11457010.1016/j.jphotochem.2023.114570 ↗
7. 10.1021/acs.macromol.8b0126310.1021/acs.macromol.8b01263 ↗
8. 10.1016/j.jphotochem.2013.08.01110.1016/j.jphotochem.2013.08.011 ↗
9. 10.1002/pi.446810.1002/pi.4468 ↗
10. 10.1126/science.aau711410.1126/science.aau7114 ↗
11. 10.1021/acsmacrolett.9b0041210.1021/acsmacrolett.9b00412 ↗
12. 10.1021/acs.accounts.0c0049510.1021/acs.accounts.0c00495 ↗
13. 10.1021/acscatal.4c0097210.1021/acscatal.4c00972 ↗
14. 10.1126/science.add697510.1126/science.add6975 ↗
15. 10.1021/jacs.8b1366310.1021/jacs.8b13663 ↗
16. 10.1021/acs.macromol.3c0012810.1021/acs.macromol.3c00128 ↗
17. 10.1021/acs.chemmater.1c0329810.1021/acs.chemmater.1c03298 ↗
18. 10.1002/advs.20220077010.1002/advs.202200770 ↗
19. 10.1021/acs.macromol.2c0124410.1021/acs.macromol.2c01244 ↗
20. 10.1021/ma020948910.1021/ma0209489 ↗
21. 10.1021/acsami.2c1441110.1021/acsami.2c14411 ↗
22. 10.1016/0022-3697(61)90076-210.1016/0022-3697(61)90076-2 ↗
23. 10.1039/D0CS00475H10.1039/D0CS00475H ↗
24. 10.1038/s41586-018-0054-x10.1038/s41586-018-0054-x ↗
25. 10.1002/app.1985.07030070710.1002/app.1985.070300707 ↗
26. The National Institute for Occupational Safety and Health; Pocket Guide to Chemical Hazards; Dicyclopentadiene; RN 77‐73‐6;https://www.cdc.gov/niosh/npg/npgd0204.html(accessed: January 2024).
27. 10.1126/sciadv.aau872310.1126/sciadv.aau8723 ↗
28. 10.1021/acsmacrolett.0c0046510.1021/acsmacrolett.0c00465 ↗
29. 10.1021/acs.macromol.3c0217710.1021/acs.macromol.3c02177 ↗