journal article·2023-03-10Open access

High-Barrier Biobased Copolyesters with Targeted Glass Transition Temperatures as Renewable Alternatives for PET

Asmaa M. Ahmed, Tuomo P. Kainulainen, Juho Antti Sirviö, Juha P. Heiskanen

ACS Applied Polymer Materials· Volume 5· Issue 3

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.
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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 ↗