journal article·2025-10Open access

Fabrication of Superinsulating Poly(Urethane‐Isocyanurate) Aerogels Derived from Upcycled Polycarbonate

Ivona Glišić, Keita Saito, Chang‐lin Wang, Christos Pantazidis, Fabian Eisenreich, Željko Tomović

Advanced Sustainable Systems· Volume 9· Issue 10

Abstract

Abstract Upcycling plastic waste into advanced functional materials is a sustainable approach to mitigate plastic accumulation and its associated environmental hazards. In this work, bisphenol‐A polycarbonate (BPA‐PC) is upcycled into an aromatic Mannich polyol (MP) via a simple one‐pot process combining organocatalyzed methanolysis followed by a Mannich reaction. MP further serves as a precursor for poly(urethane‐isocyanurate) (PUR‐PIR) aerogels. The resulting PUR‐PIR aerogels are prepared with different isocyanate indices and demonstrate low bulk densities (<195 mg cm −3 ), and high specific surface areas (≈ 200 m 2 g −1 ), along with outstanding mechanical performance, and ultralow thermal conductivity (≈ 17 mW m −1 K −1 ). Importantly, PUR‐PIR aerogels prepared from pristine or waste BPA‐PC exhibit comparable material performance. This work highlights the potential of upcycling plastic waste into superinsulating aerogels with tunable material properties.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Aerogels and thermal insulation · Advanced Sensor and Energy Harvesting Materials · Surface Modification and Superhydrophobicity

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Polymer Performance Materials Group Department of Chemical Engineering and Chemistry and Institute for Complex Molecular Systems (ICMS) Eindhoven University of Technology Eindhoven 5600 MB The Netherlands

Funding

Ministerie van Onderwijs, Cultuur en Wetenschap

References (42)

Show source-provided references
1. 10.1098/rstb.2008.030410.1098/rstb.2008.0304 ↗
2. 10.1126/sciadv.170078210.1126/sciadv.1700782 ↗
3. 10.1016/j.chemosphere.2023.13808910.1016/j.chemosphere.2023.138089 ↗
4. 10.1039/C7GC01496A10.1039/C7GC01496A ↗
5. 10.1126/science.abg450310.1126/science.abg4503 ↗
6. 10.1002/smll.20240393110.1002/smll.202403931 ↗
7. 10.1002/adfm.20242047210.1002/adfm.202420472 ↗
8. 10.1080/10408398.2010.53691910.1080/10408398.2010.536919 ↗
9. 10.1201/978148227369410.1201/9781482273694 ↗
10. Kyriacos D. · 2017
11. 10.1039/C9PY01927H10.1039/C9PY01927H ↗
12. 10.1021/ie404263a10.1021/ie404263a ↗
13. 10.1039/D2GC03568E10.1039/D2GC03568E ↗
14. 10.1039/C7GC02063E10.1039/C7GC02063E ↗
15. 10.1016/j.polymer.2018.04.01510.1016/j.polymer.2018.04.015 ↗
16. 10.1002/anie.20221180610.1002/anie.202211806 ↗
17. 10.1073/pnas.160092411310.1073/pnas.1600924113 ↗
18. 10.1021/acssuschemeng.4c1014110.1021/acssuschemeng.4c10141 ↗
19. Randall D. · 2003
20. 10.1002/macp.20200011410.1002/macp.202000114 ↗
21. 10.3390/ma1110184110.3390/ma11101841 ↗
22. 10.1016/j.jobe.2021.10260410.1016/j.jobe.2021.102604 ↗
23. 10.1016/j.polymer.2014.10.00610.1016/j.polymer.2014.10.006 ↗
24. 10.1016/j.enbuild.2010.12.01210.1016/j.enbuild.2010.12.012 ↗
25. 10.1007/978-1-4419-7589-810.1007/978-1-4419-7589-8 ↗
26. Ionescu M. · 2005
27. 10.1021/acsami.4c0748010.1021/acsami.4c07480 ↗
28. 10.1016/S0022-3093(98)00103-310.1016/S0022-3093(98)00103-3 ↗
29. 10.1021/acsapm.1c0071210.1021/acsapm.1c00712 ↗
30. 10.1021/acsami.7b0334410.1021/acsami.7b03344 ↗
31. 10.1021/acs.chemmater.7b0102010.1021/acs.chemmater.7b01020 ↗
32. 10.1021/acsapm.1c0098710.1021/acsapm.1c00987 ↗
33. 10.1016/j.polymer.2018.04.01510.1016/j.polymer.2018.04.015 ↗
34. Rotaru I. · U.P.B. Sci. Bull. Ser. B · 2007 · 69 · 35
35. 10.1007/s10924-015-0717-810.1007/s10924-015-0717-8 ↗
36. 10.1515/polyeng-2014-017610.1515/polyeng-2014-0176 ↗
37. 10.1002/cctc.20220136210.1002/cctc.202201362 ↗
38. 10.1021/acsapm.3c0088210.1021/acsapm.3c00882 ↗
39. 10.1021/cm401623h10.1021/cm401623h ↗
40. 10.1007/s10971-023-06282-910.1007/s10971-023-06282-9 ↗
41. 10.3390/nano1214240910.3390/nano12142409 ↗
42. 10.1016/j.rser.2020.11003810.1016/j.rser.2020.110038 ↗