Biobased Transparent Thiol–Ene Polymer Networks from Levoglucosan
Source abstract
Abstract
Developing thermosets from renewable feedstocks for the production of sustainable polymer networks is of great significance as the world transitions from its heavy reliance on petroleum-derived polymeric materials. Levoglucosan is a renewable chemical, obtained from the pyrolysis of cellulosic biomass and was selected for this study due to its rich functionality. Allyl and pentenoyl levoglucosan monomers were synthesized with selective chemical functionality and were rapidly cured via ultraviolet (UV)-initiated thiol–ene click chemistry to obtain optically transparent, degradable networks. The mechanical properties (tensile strength and Young’s modulus) and glass-transition temperature are tunable over the range of 1.08–3.40, 2.50–4.72 MPa, and 3.93–22.8 °C based on the monomer compositions. The resulting thermosets are able to be tailored for desired properties and applications, as demonstrated by stereolithography (SLA) three-dimensional (3D) printing and postcuring modification.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: biodegradable polymer synthesis and properties · Polymer composites and self-healing · Lignin and Wood Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Natural Sciences─Chemistry, University of Tasmania, Hobart, Tasmania 7005, Australia
Centre for Sustainable Architecture with Wood (CSAW), University of Tasmania, Launceston, Tasmania 7250, Australia
Funding
Department of Education, Skills and Employment, Australian Government
References (31)
Show source-provided references
1. Geyer R. · 2020 · 1310.1016/B978-0-12-817880-5.00002-5 ↗
2. 10.1016/j.trechm.2019.03.00410.1016/j.trechm.2019.03.004 ↗
3. 10.1002/bbb.200410.1002/bbb.2004 ↗
4. 10.1039/C9GC02461A10.1039/C9GC02461A ↗
5. 10.1021/acssuschemeng.0c0481710.1021/acssuschemeng.0c04817 ↗
6. 10.1021/acssuschemeng.8b0235510.1021/acssuschemeng.8b02355 ↗
7. 10.1039/D0PY01222J10.1039/D0PY01222J ↗
8. 10.1016/j.ijbiomac.2015.10.04010.1016/j.ijbiomac.2015.10.040 ↗
9. 10.1021/acssuschemeng.9b0116110.1021/acssuschemeng.9b01161 ↗
10. 10.1039/D3GC01833D10.1039/D3GC01833D ↗
11. 10.1016/j.porgcoat.2022.10720310.1016/j.porgcoat.2022.107203 ↗
12. 10.1021/acsapm.2c0035810.1021/acsapm.2c00358 ↗
13. 10.1002/mame.20220049710.1002/mame.202200497 ↗
14. 10.1039/C7SC00936D10.1039/C7SC00936D ↗
15. 10.1016/j.eurpolymj.2016.02.02510.1016/j.eurpolymj.2016.02.025 ↗
16. 10.1002/pola.2036610.1002/pola.20366 ↗
17. 10.1002/anie.20090392410.1002/anie.200903924 ↗
18. 10.1039/c1lc20388f10.1039/c1lc20388f ↗
19. 10.1039/C7MH00488E10.1039/C7MH00488E ↗
20. 10.1016/j.eurpolymj.2018.03.00510.1016/j.eurpolymj.2018.03.005 ↗
21. 10.1002/pol.2019029110.1002/pol.20190291 ↗
22. 10.1016/j.eurpolymj.2014.11.01310.1016/j.eurpolymj.2014.11.013 ↗
23. 10.1039/D0PY01407A10.1039/D0PY01407A ↗
24. 10.1039/D2GC04185E10.1039/D2GC04185E ↗
25. 10.1039/D2SC00146B10.1039/D2SC00146B ↗
26. 10.1039/D2GC02901D10.1039/D2GC02901D ↗
27. 10.1016/j.cej.2022.14005110.1016/j.cej.2022.140051 ↗
28. 10.1016/j.porgcoat.2017.10.02510.1016/j.porgcoat.2017.10.025 ↗
29. 10.1039/C9GC03931G10.1039/C9GC03931G ↗
30. 10.1021/acs.macromol.3c0010810.1021/acs.macromol.3c00108 ↗
31. 10.1016/j.carbpol.2018.09.02710.1016/j.carbpol.2018.09.027 ↗