journal article·2025-03-14Open access

Synthesis and Characterization of Photo-Crosslinkable Coumarin-Based Poly(lactic acid) as a Promising Material for 3D Printing Applications

Antoni Pagés-Llobet, Fernando Julián, Francesc Xavier Espinach, Heura Ventura, Helena Oliver-Ortega, José Alberto Méndez

ACS Applied Polymer Materials· Volume 7· Issue 5

Abstract

Poly(lactic acid) (PLA) is a biopolymer that resembles oil-based plastics in its mechanical properties. However, in manufacturing techniques such as fused deposition modeling (FDM), the inherent characteristics of the process led to a reduction in the mechanical properties of PLA-based pieces. To improve the material performance, one strategy is photo-cross-linking PLA chains. Functionalization of PLA requires grafting a molecule capable of reacting with it and ultimately cross-linking the polymeric chains. In this research, methacrylate coumarin was incorporated into PLA via free-radical grafting under reactive extrusion conditions for 5 min. The highest grafting degree value was 0.7% after the addition of 10 and 5 wt % coumarin and dicumylperoxide, respectively. Thereafter, a thin film of the material was ultraviolet (UV)-exposed for 48 h, and photo-cross-linking was confirmed with a gel formation of 16.9%. As a result, the thermal stability and melt strength of pure PLA increased by 7 °C and 1 order of magnitude, respectively. Finally, the tensile properties were evaluated by printing 3D specimens. Photo-cross-linked films were blended with nonirradiated coumarin-based PLA to obtain high infill density values (89% ± 0.8). The mechanical strength (17.8%) and stiffness (26%) of the neat PLA were enhanced.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: biodegradable polymer synthesis and properties · Photopolymerization techniques and applications · Additive Manufacturing and 3D Printing Technologies

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

Affiliations

LEPAMAP-PRODIS Research Group, Department of Chemical Engineering, Agriculture and Food Technology, Universitat de Girona, Maria Aurèlia Capmany 61, 17003 Girona, Spain

Departament de Ciència i Enginyeria de Materials, Universitat Politècnica de Catalunya, Colom 1, 08222 Terrassa, Spain

Institut d’Investigació Tèxtil i Cooperació Industrial de Terrassa (INTEXTER), Colom 15, 08222 Terrassa, Spain

Funding

Ministerio de Ciencia, Innovaci?n y Universidades · Departament d'Innovaci?, Universitats i Empresa, Generalitat de Catalunya

References (46)

Show source-provided references
1. 10.1038/s41578-021-00407-810.1038/s41578-021-00407-8 ↗
2. 10.3390/ma1512431210.3390/ma15124312 ↗
3. 10.3390/polym1311182210.3390/polym13111822 ↗
4. 10.3390/polym1401001510.3390/polym14010015 ↗
5. 10.3390/ma1624766410.3390/ma16247664 ↗
6. 10.3390/polym1319336810.3390/polym13193368 ↗
7. 10.3390/polym1509201910.3390/polym15092019 ↗
8. 10.1515/rams-2023-014010.1515/rams-2023-0140 ↗
9. 10.1016/j.matdes.2023.11168710.1016/j.matdes.2023.111687 ↗
10. 10.3390/polym1309140710.3390/polym13091407 ↗
11. 10.1039/C7PY01385J10.1039/C7PY01385J ↗
12. 10.1016/j.ijbiomac.2024.13498410.1016/j.ijbiomac.2024.134984 ↗
13. Clayden, J.; Greeves, N.; Warren, S. Organic Chemistry.; Oxford University Press: Oxford, 2000; p 1536.
14. 10.1039/C5RA00894H10.1039/C5RA00894H ↗
15. 10.3390/ma1503116110.3390/ma15031161 ↗
16. 10.1016/j.molstruc.2022.13270210.1016/j.molstruc.2022.132702 ↗
17. 10.1016/j.polymdegradstab.2013.10.00110.1016/j.polymdegradstab.2013.10.001 ↗
18. 10.1016/j.polymdegradstab.2018.02.01110.1016/j.polymdegradstab.2018.02.011 ↗
19. 10.1002/pat.618010.1002/pat.6180 ↗
20. 10.1021/ma010946910.1021/ma0109469 ↗
21. 10.1016/j.tet.2014.07.01910.1016/j.tet.2014.07.019 ↗
22. 10.3390/polym1316274110.3390/polym13162741 ↗
23. 10.1002/pen.2330410.1002/pen.23304 ↗
24. 10.1080/02678290020277810.1080/026782900202778 ↗
25. 10.1021/om100106e10.1021/om100106e ↗
26. 10.1016/j.polymer.2019.12166910.1016/j.polymer.2019.121669 ↗
27. 10.1016/j.eurpolymj.2016.02.01610.1016/j.eurpolymj.2016.02.016 ↗
28. 10.1007/s10924-012-0544-010.1007/s10924-012-0544-0 ↗
29. 10.1021/acs.iecr.2c0127610.1021/acs.iecr.2c01276 ↗
30. 10.1051/meca/201905210.1051/meca/2019052 ↗
31. 10.1080/15583724.2020.185519410.1080/15583724.2020.1855194 ↗
32. 10.1038/pj.2010.4210.1038/pj.2010.42 ↗
33. 10.1002/app.4172410.1002/app.41724 ↗
34. 10.1021/acsomega.8b0090710.1021/acsomega.8b00907 ↗
35. 10.1016/j.reactfunctpolym.2020.10475010.1016/j.reactfunctpolym.2020.104750 ↗
36. 10.1016/j.compositesb.2022.10990110.1016/j.compositesb.2022.109901 ↗
37. 10.1016/j.carbpol.2007.10.01010.1016/j.carbpol.2007.10.010 ↗
38. 10.1016/j.polymertesting.2008.08.00910.1016/j.polymertesting.2008.08.009 ↗
39. 10.1002/pat.386410.1002/pat.3864 ↗
40. 10.1007/s12221-022-4857-x10.1007/s12221-022-4857-x ↗
41. 10.1080/15583724.2019.157218510.1080/15583724.2019.1572185 ↗
42. 10.3390/molecules2515349710.3390/molecules25153497 ↗
43. 10.1021/acs.macromol.2c0137410.1021/acs.macromol.2c01374 ↗
44. 10.3390/molecules2521491910.3390/molecules25214919 ↗
45. 10.1016/j.msec.2021.11257610.1016/j.msec.2021.112576 ↗
46. 10.1016/j.jmrt.2021.10.10810.1016/j.jmrt.2021.10.108 ↗