Tuning Curing, Latency, and Dynamic Behavior in Optically Clear Epoxy Vitrimers Using Organotin Catalysts
Source abstract
Abstract
Achieving optically clear epoxy vitrimers based on transesterification remains a significant challenge. While epoxy vitrimer systems offer high thermomechanical performance, optical clarity is often compromised by catalyst-induced side reactions and network heterogeneities and has rarely been demonstrated in conventional epoxy–acid formulations, particularly after reprocessing. In this work, we examine how two commercially available tin oxides, monobutyltin oxide (MBTO) and dibutyltin oxide (DBTO), govern the curing pathways, topology, and relaxation behavior of transparent epoxy vitrimer networks. Differences in Lewis acidity, solubility, and steric hindrance result in different efficiencies for esterification and transesterification. MBTO strongly accelerates epoxy–acid polyaddition, whereas DBTO enhances latency and can favor interfacial exchange during heterogeneous vitrimerization. Both vitrimers remain reprocessable at 200 °C, achieving good thermomechanical recovery after reprocessing, consistent with the thermal robustness of the catalysts. Importantly, the original and reprocessed materials maintain high optical transparency across the UV–visible region, underscoring their potential in applications requiring clear, reprocessable materials. Overall, these results show that catalyst selection can tune reactivity, latency, and dynamic response, guiding the design of transparent, thermally resistant, and recyclable epoxy vitrimers.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polymer composites and self-healing · Flame retardant materials and properties · Lignin and Wood Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering
Monash University
CNRS, Université de Lorraine, UMR 7274
Department of Mechanical and Aerospace Engineering
Bioresource Processing Research Institute of Australia (BioPRIA)
Funding
Australian Research Council (ARC)
References (52)
Show source-provided references
1. 10.1126/science.121264810.1126/science.1212648 ↗
2. 10.3390/polym1208166010.3390/polym12081660 ↗
3. 10.1021/mz300239f10.1021/mz300239f ↗
4. 10.1039/D0SC01069C10.1039/D0SC01069C ↗
5. 10.1039/C5SC02223A10.1039/C5SC02223A ↗
6. 10.1016/j.progpolymsci.2020.10123310.1016/j.progpolymsci.2020.101233 ↗
7. Thomas, R.; Sinturel, C.; Thomas, S.; Sadek El Akiaby, E. M. Introduction ; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2014; pp 1–30.10.1002/9783527666874.ch1 ↗
8. 10.1021/acsapm.3c0027210.1021/acsapm.3c00272 ↗
9. 10.1002/macp.20250027610.1002/macp.202500276 ↗
10. 10.1021/acsapm.0c0039710.1021/acsapm.0c00397 ↗
11. 10.1016/j.compscitech.2021.10869010.1016/j.compscitech.2021.108690 ↗
12. 10.1002/gch2.20180007610.1002/gch2.201800076 ↗
13. 10.1016/j.compositesa.2020.10583710.1016/j.compositesa.2020.105837 ↗
14. 10.1021/acsomega.2c0267710.1021/acsomega.2c02677 ↗
15. 10.1021/acs.iecr.6b0382910.1021/acs.iecr.6b03829 ↗
16. 10.1021/acs.macromol.5c0235410.1021/acs.macromol.5c02354 ↗
17. 10.1039/D4LP00112E10.1039/D4LP00112E ↗
18. 10.3390/polym1009101710.3390/polym10091017 ↗
19. 10.1021/acsapm.3c0077810.1021/acsapm.3c00778 ↗
20. 10.1134/S207005042004007810.1134/S2070050420040078 ↗
21. Bossert, E. C. Introduction to organotin chemistry and applications 2000 https://www.gelest.com/wp-content/uploads/13Tin.pdf.
22. 10.1039/C4CY01535E10.1039/C4CY01535E ↗
23. 10.2174/245227160566622040414460410.2174/2452271605666220404144604 ↗
24. 10.1021/acs.macromol.1c0086110.1021/acs.macromol.1c00861 ↗
25. 10.1021/acsmacrolett.0c0029910.1021/acsmacrolett.0c00299 ↗
26. 10.1002/gch2.20180007610.1002/gch2.201800076 ↗
27. 10.1016/j.polymdegradstab.2024.11082010.1016/j.polymdegradstab.2024.110820 ↗
28. 10.1039/D0PY00342E10.1039/D0PY00342E ↗
29. 10.1021/ja01856a06110.1021/ja01856a061 ↗
30. 10.1063/1.172392210.1063/1.1723922 ↗
31. 10.3390/polym1001004310.3390/polym10010043 ↗
32. 10.1021/ja302894k10.1021/ja302894k ↗
33. 10.1039/C6RA18010H10.1039/C6RA18010H ↗
34. 10.1021/acs.biomac.1c0082010.1021/acs.biomac.1c00820 ↗
35. 10.1016/j.pmatsci.2020.10071010.1016/j.pmatsci.2020.100710 ↗
36. 10.1039/D2MA00654E10.1039/D2MA00654E ↗
37. 10.1039/C3RA47438K10.1039/C3RA47438K ↗
38. 10.1002/pol.2020011810.1002/pol.20200118 ↗
39. 10.1002/app.5323310.1002/app.53233 ↗
40. 10.1016/j.apcata.2012.07.04010.1016/j.apcata.2012.07.040 ↗
41. 10.5402/2012/14285710.5402/2012/142857 ↗
42. 10.1016/j.fuproc.2012.08.01510.1016/j.fuproc.2012.08.015 ↗
43. 10.1016/j.apcata.2009.06.00210.1016/j.apcata.2009.06.002 ↗
44. 10.1021/acs.macromol.8b0142410.1021/acs.macromol.8b01424 ↗
45. 10.1016/j.compscitech.2017.11.00610.1016/j.compscitech.2017.11.006 ↗
46. 10.1016/j.mattod.2021.07.00310.1016/j.mattod.2021.07.003 ↗
47. McKeen L. W. · 2012 · 5710.1016/B978-1-4557-2598-4.00003-4 ↗
48. 10.1039/C6CP00924G10.1039/C6CP00924G ↗
49. 10.1016/S0926-860X(03)00647-110.1016/S0926-860X(03)00647-1 ↗
50. 10.1021/acsomega.3c0133610.1021/acsomega.3c01336 ↗
51. 10.56530/spectroscopy.ly3071f510.56530/spectroscopy.ly3071f5 ↗
52. 10.1016/j.polymdegradstab.2012.04.00710.1016/j.polymdegradstab.2012.04.007 ↗