A Fully Biobased Aromatic Polyester Polyol for Polyisocyanurate Rigid Foams: Poly(diethylene furanoate)
Source abstract
Abstract
Aromatic polyester polyols are often used in polyurethane rigid foam (PUR) and polyisocyanurate (PIR) synthesis, since they offer higher rigidity than polyether polyols. Herein, a route toward fully biobased aromatic polyester polyols was investigated using sugar-based 2,5-furandicarboxylic acid (FDCA) and diethylene glycol (DEG), enabling a direct one-step synthesis of a fully biobased aromatic polyester polyol, poly(diethylene furanoate) (PDEF), for applications in PIR rigid foam. Therefore, reaction conditions were optimized to obtain PDEF as a processable polyol with OH values and remaining unreacted DEG similar to a commercial, petroleum-based polyol. The processability was improved by either copolymerizing 10–20 mol % of a biobased aliphatic dicarboxylic acid, like succinic acid (SA) or adipic acid (AA), maintaining the fully biobased character of the polyol, or copolymerization with phthalic acid. The fully biobased polyester polyols were successfully prepared on a 100 g scale of dicarboxylic acids. Subsequent application in PIR rigid foam showed similar density, thermal conductivity, flame behavior, and compressive strength if compared to the rigid foam obtained from a commercial polyol. Thus, fully biobased PDEF can substitute petroleum-based aromatic polyester polyols in PIR applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: biodegradable polymer synthesis and properties · Polymer composites and self-healing · Synthesis and properties of polymers
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Laboratory of Applied Chemistry, Institute of Organic Chemistry (IOC), Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany
puren GmbH, Rengoldshauser Str. 4, 88662 Überlingen, Deutschland
Laboratory of Applied Chemistry, Institute of Biological and Chemical Systems−Functional Molecular Systems (IBCS-FMS), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen, Germany
Funding
puren gmbh
References (38)
Show source-provided references
1. Plastics Europe2021, https://plasticseurope.org/de/knowledge-hub/plastics-the-facts-2019/ (accessed 15-11-2021).
2. European bioplastics2021, https://www.european-bioplastics.org/market/ (accessed 15-11-2021).
3. 10.1039/C8PY00827B10.1039/C8PY00827B ↗
4. 10.1021/acs.biomac.0c0161010.1021/acs.biomac.0c01610 ↗
5. 10.1002/anie.20130276610.1002/anie.201302766 ↗
6. 10.1016/S0011-2275(97)00120-310.1016/S0011-2275(97)00120-3 ↗
7. 10.1002/cber.1930063042210.1002/cber.19300630422 ↗
8. 10.1002/cber.18700030121510.1002/cber.187000301215 ↗
9. 10.1177/0021955X880240060610.1177/0021955X8802400606 ↗
10. 10.1016/S0141-3910(02)00086-110.1016/S0141-3910(02)00086-1 ↗
11. 10.1002/app.4383310.1002/app.43833 ↗
12. 10.3390/molecules2207109110.3390/molecules22071091 ↗
13. 10.1016/j.eurpolymj.2016.10.01210.1016/j.eurpolymj.2016.10.012 ↗
14. 10.7569/JRM.2014.63413210.7569/JRM.2014.634132 ↗
15. Čuk N. · J. Appl. Polym. Sci. · 2015 · 132 · 4152210.1002/app.41522 ↗
16. 10.1016/j.polymertesting.2013.03.01010.1016/j.polymertesting.2013.03.010 ↗
17. 10.1177/073168440809694910.1177/0731684408096949 ↗
18. Chuayjuljit S. · J. Met. Mater. Miner. · 2017 · 17 · 17
19. 10.1002/app.191310.1002/app.1913 ↗
20. 10.1016/j.progpolymsci.2016.02.00210.1016/j.progpolymsci.2016.02.002 ↗
21. Wilson, C. L.; Benning, C. J., Method of Making Polyester Composition. US2863855A 1958.
22. 10.1177/0021955X0303506710.1177/0021955X03035067 ↗
23. 10.1080/10643389.2020.181849610.1080/10643389.2020.1818496 ↗
24. Ionescu M. · 2005
25. 10.1021/i360005a00610.1021/i360005a006 ↗
26. 10.1007/s00289-016-1705-410.1007/s00289-016-1705-4 ↗
27. 10.1016/j.eurpolymj.2017.10.02010.1016/j.eurpolymj.2017.10.020 ↗
28. Hostettler, F.; Young, D. M., Lactone Polyester. US3169945A 1965.
29. Hostettler, F.; Young, D. M., Polyurethane Polymers from Lactone Polyesters. US3186971A 1965.
30. 10.1080/10643389.2016.118022710.1080/10643389.2016.1180227 ↗
31. 10.1002/mame.20040018610.1002/mame.200400186 ↗
32. 10.1021/ie501995m10.1021/ie501995m ↗
33. 10.1002/app.1988.07035031710.1002/app.1988.070350317 ↗
34. 10.1016/j.biortech.2011.11.06910.1016/j.biortech.2011.11.069 ↗
35. 10.1016/j.apcatb.2014.08.02610.1016/j.apcatb.2014.08.026 ↗
36. 10.1016/j.biombioe.2010.12.00610.1016/j.biombioe.2010.12.006 ↗
37. 10.1021/acs.iecr.8b0358910.1021/acs.iecr.8b03589 ↗
38. 10.1002/cssc.20120065210.1002/cssc.201200652 ↗