Cellulose Nanocrystals: Accelerator and Reinforcing Filler for Epoxy Vitrimerization
Source abstract
Abstract
The novel vitrimerization concept of converting permanently cross-linked networks of thermoset polymers into dynamic exchangeable networks often relies on transesterification reactions. Transesterification exchange reactions, for example, in epoxy vitrimers, are usually contingent on equivalent ratios of hydroxyl to ester groups and large amounts of catalysts to achieve proper dynamic exchange capability. In general, postconsumer epoxy cured with anhydrides contains very few hydroxyl groups in the network, and it is challenging to convert it into efficient dynamic networks by vitrimerization. Here, we demonstrate that introducing cellulose nanocrystals as feedstock of external hydroxyl groups in the mechanochemical vitrimerization process could improve the exchange reaction rate as well as the thermomechanical properties of the vitrimerized epoxy. This work offers an effective way to recycle and reprocess postconsumer epoxy/anhydride waste with inherent low ratios of hydroxyl to ester groups into higher value-added vitrimer nanocomposites.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polymer composites and self-healing · Lignin and Wood Chemistry · Electrospun Nanofibers in Biomedical Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Macromolecular Science and Engineering, Case Western Reserve University, 2100 Adelbert Road, Kent Hale Smith Bldg, Cleveland, Ohio 44106, United States
College of Polymer Science and Engineering, Sichuan University, Chengdu 610065, Sichuan, China
Department of Chemistry, Case Western Reserve University, 2080 Adelbert Road, Cleveland Ohio 44106, United States
Funding
Air Force Office of Scientific Research · National Science Foundation
References (33)
Show source-provided references
1. 10.1021/sc500478f10.1021/sc500478f ↗
2. Gibson, G. Epoxy Resins; 2017.10.1016/B978-0-323-35824-8.00027-X ↗
3. 10.1016/j.polymdegradstab.2018.08.00610.1016/j.polymdegradstab.2018.08.006 ↗
4. 10.1021/acssuschemeng.8b0235510.1021/acssuschemeng.8b02355 ↗
5. 10.1002/gch2.20190008110.1002/gch2.201900081 ↗
6. 10.1126/science.121264810.1126/science.1212648 ↗
7. 10.1016/j.polymer.2020.12239210.1016/j.polymer.2020.122392 ↗
8. 10.1021/acsmacrolett.0c0029910.1021/acsmacrolett.0c00299 ↗
9. 10.1002/gch2.20180007610.1002/gch2.201800076 ↗
10. 10.1021/acssuschemeng.0c0481510.1021/acssuschemeng.0c04815 ↗
11. 10.1021/acs.macromol.9b0189610.1021/acs.macromol.9b01896 ↗
12. 10.1039/D0PY00342E10.1039/D0PY00342E ↗
13. 10.1016/0032-3861(83)90203-310.1016/0032-3861(83)90203-3 ↗
14. 10.1016/j.polymer.2007.04.04210.1016/j.polymer.2007.04.042 ↗
15. 10.1007/s10570-012-9768-310.1007/s10570-012-9768-3 ↗
16. 10.1016/j.pmatsci.2017.01.00310.1016/j.pmatsci.2017.01.003 ↗
17. 10.1039/C8NA00238J10.1039/C8NA00238J ↗
18. 10.1021/acssuschemeng.9b0280010.1021/acssuschemeng.9b02800 ↗
19. 10.1039/C3GC40965A10.1039/C3GC40965A ↗
20. 10.1007/s10570-018-2197-110.1007/s10570-018-2197-1 ↗
21. 10.1039/B108255H10.1039/B108255H ↗
22. 10.1021/acssuschemeng.8b0037510.1021/acssuschemeng.8b00375 ↗
23. 10.1039/C5RA08690F10.1039/C5RA08690F ↗
24. 10.1021/acsmacrolett.9b0002410.1021/acsmacrolett.9b00024 ↗
25. 10.1016/j.compscitech.2019.06.00410.1016/j.compscitech.2019.06.004 ↗
26. 10.1021/mz300239f10.1021/mz300239f ↗
27. 10.1021/ja302894k10.1021/ja302894k ↗
28. 10.1021/acs.macromol.8b0142410.1021/acs.macromol.8b01424 ↗
29. 10.1021/acssuschemeng.8b0607310.1021/acssuschemeng.8b06073 ↗
30. 10.1016/j.compositesa.2020.10580110.1016/j.compositesa.2020.105801 ↗
31. 10.1002/marc.20190031310.1002/marc.201900313 ↗
32. 10.1021/am900830h10.1021/am900830h ↗
33. 10.1021/acsami.8b1910010.1021/acsami.8b19100 ↗