High-Barrier Biobased Copolyesters with Targeted Glass Transition Temperatures as Renewable Alternatives for PET
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide A series of amorphous furan-based copolyesters were investigated with the goal of matching the glass transition temperature ( T g ) of poly(ethylene terephthalate) (PET) while providing an enhanced O 2 barrier. The biobased copolyesters were composed of dimethyl 5,5′-sulfanediyldi(furan-2-carboxylate) (DM-SFA) with either dimethyl 2,5-furandicarboxylate (DM-FDCA) or dimethyl 2,2′-bifuran-5,5′-dicarboxylate (DM-BFDCA) as the main monomers with ethylene glycol as the diol component. The furfural-based monomers DM-SFA and DM-BFDCA in roughly equimolar ratios provided copolyesters with T g in the range of PET, while also having low O 2 and UV-light permeabilities. With the 5-hydroxymethylfurfural-based DM-FDCA monomer, DM-SFA was adjusted to be the minor comonomer in the feed in order to provide PET-like T g for the copolyester. On the other hand, the O 2 permeabilities of these copolyesters were substantially lower, although the DM-FDCA monomer lacked the UV-blocking benefits of DM-BFDCA. Finally, isosorbide (IS) was also investigated as a possible T g -enhancing comonomer in conjunction with ethylene glycol and DM-SFA. However, thermal stability of the IS-containing copolyester was found to be lower, as indicated by thermogravimetric analysis. Incomplete dissolution after polycondensation was also observed, which was consistent with cross-linking under high-temperature conditions. Additionally, melt-pressed films did not completely yield at high temperatures during dynamic mechanical analysis, which contrasted with the behavior of the DM-FDCA and DM-BFDCA copolyesters. The DM-SFA/DM-BFDCA copolyesters were identified as especially interesting materials having relatively high glass transition temperatures while being completely amorphous and providing films with low O 2 and UV-light permeabilities. They are also notable for having most of their carbon derived from the renewable platform chemical furfural.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalysis for Biomass Conversion · biodegradable polymer synthesis and properties · Carbon dioxide utilization in catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Research Unit of Sustainable Chemistry, University of Oulu, P.O. Box 4300, FI-90014 Oulu, Finland
Fibre and Particle Engineering Research Unit, University of Oulu, P.O. Box 4300, FI-90014 Oulu, Finland
Funding
Jenny ja Antti Wihurin Rahasto · Magnus Ehrnroothin S??ti? · Suomen Kulttuurirahasto
References (42)
Show source-provided references
1. Plastics Europe. Compelling Facts About Plastics 2009: An analysis of European plastics production, demand and recovery for 2008; Plastics Europe: 2009. https://plasticseurope.org/wp-content/uploads/2021/10/2009-Compelling-facts.pdf (accessed 2021-01-06).
2. 10.1098/rstb.2008.030410.1098/rstb.2008.0304 ↗
3. 10.3390/polym1416341210.3390/polym14163412 ↗
4. 10.4028/www.scientific.net/AMM.312.40610.4028/www.scientific.net/AMM.312.406 ↗
5. 10.1039/C9PY01128E10.1039/C9PY01128E ↗
6. 10.1038/nature2100110.1038/nature21001 ↗
7. 10.1002/macp.20120043910.1002/macp.201200439 ↗
8. 10.1039/c0gc00789g10.1039/c0gc00789g ↗
9. 10.1021/acs.chemrev.7b0039510.1021/acs.chemrev.7b00395 ↗
10. 10.1021/mz400207g10.1021/mz400207g ↗
11. 10.1016/j.progpolymsci.2013.05.00610.1016/j.progpolymsci.2013.05.006 ↗
12. 10.1039/C5GC01771H10.1039/C5GC01771H ↗
13. 10.3390/polym1405094310.3390/polym14050943 ↗
14. 10.3389/fchem.2020.0058510.3389/fchem.2020.00585 ↗
15. 10.1002/pola.2852710.1002/pola.28527 ↗
16. 10.1016/j.polymer.2014.07.04110.1016/j.polymer.2014.07.041 ↗
17. 10.1021/acs.macromol.5b0033310.1021/acs.macromol.5b00333 ↗
18. 10.1021/acs.macromol.8b0010810.1021/acs.macromol.8b00108 ↗
19. 10.1021/acs.macromol.8b0019210.1021/acs.macromol.8b00192 ↗
20. 10.1021/ma500019910.1021/ma5000199 ↗
21. Reese G. · 2003 · 3 · 652
22. 10.1021/acs.iecr.1c0062910.1021/acs.iecr.1c00629 ↗
23. 10.3390/polym1206120910.3390/polym12061209 ↗
24. 10.1002/app.4718610.1002/app.47186 ↗
25. 10.1016/j.polymer.2012.11.08110.1016/j.polymer.2012.11.081 ↗
26. 10.1016/j.eurpolymj.2017.02.03710.1016/j.eurpolymj.2017.02.037 ↗
27. 10.1002/pol.2019005710.1002/pol.20190057 ↗
28. 10.1021/acs.macromol.7b0245710.1021/acs.macromol.7b02457 ↗
29. 10.1021/acs.iecr.0c0420310.1021/acs.iecr.0c04203 ↗
30. 10.1016/j.polymer.2020.12225810.1016/j.polymer.2020.122258 ↗
31. 10.1246/cl.17064710.1246/cl.170647 ↗
32. 10.1016/j.polymdegradstab.2022.10996010.1016/j.polymdegradstab.2022.109960 ↗
33. 10.1021/acs.biomac.9b0144710.1021/acs.biomac.9b01447 ↗
34. 10.1021/acs.biomac.2c0009710.1021/acs.biomac.2c00097 ↗
35. 10.1016/j.progpolymsci.2019.10119610.1016/j.progpolymsci.2019.101196 ↗
36. 10.1016/j.eurpolymj.2021.11096410.1016/j.eurpolymj.2021.110964 ↗
37. 10.1016/j.progpolymsci.2009.10.00110.1016/j.progpolymsci.2009.10.001 ↗
38. 10.1039/D2GC02608B10.1039/D2GC02608B ↗
39. Farah S. · 2015 · 14310.1016/B978-0-323-31306-3.00008-7 ↗
40. 10.1002/star.1986038010710.1002/star.19860380107 ↗
41. 10.1016/j.polymer.2016.09.03010.1016/j.polymer.2016.09.030 ↗
42. 10.1039/C6GC01060A10.1039/C6GC01060A ↗