Bio-based epoxy resin from gallic acid and its thermosets toughened with renewable tannic acid derivatives
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Abstract
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OpenAlex topics: Polymer composites and self-healing · Lignin and Wood Chemistry · Epoxy Resin Curing Processes
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References (50)
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1. Wan J, Gan B, Li C, Molina-Aldareguia J, Li Z, Wang X (2015) A novel biobased epoxy resin with high mechanical stiffness and low flammability: synthesis, characterization and properties. J Mater Chem A 3(43):21907–2192110.1039/C5TA02939B ↗
2. Zhang Q, Molenda M, Reineke T-M (2016) Epoxy resin thermosets derived from trehalose and β-cyclodextrin. Macromolecules 49(22):8397–840610.1021/acs.macromol.6b01861 ↗
3. Yang J, He X, Wang H, Liu X, Lin P, Yang S, Fu S (2020) High-toughness, environment-friendly solid epoxy resins: Preparation, mechanical performance, curing behavior, and thermal properties. J Appl Polym Sci 137(17):4859610.1002/app.48596 ↗
4. Aouf C, Lecomte J, Villeneuve P (2012) Chemo-enzymatic functionalization of gallic and vanillic acids: synthesis of bio-based epoxy resins prepolymers. Green Chem 14(8):2328–233610.1039/c2gc35558b ↗
5. Yang J, Wang H, Liu X (2021) A nano-TiO2/regenerated cellulose biohybrid enables simultaneously improved strength and toughness of solid epoxy resins. Compos Sci Technol 212:10888410.1016/j.compscitech.2021.108884 ↗
6. Lou G, Ma Z, Dai J (2021) Fully biobased surface-functionalized microcrystalline cellulose via green self-assembly toward fire-retardant, strong, and tough epoxy biocomposites. ACS Sustain Chem/Eng 9(40):13595–1360510.1021/acssuschemeng.1c04718 ↗
7. Wan J, Zhao J, Gan B (2016) Ultrastiff biobased epoxy resin with high Tg and low permittivity: from synthesis to properties. ACS Sustain Chem/Eng 4(5):2869–288010.1021/acssuschemeng.6b00479 ↗
8. Auvergne R, Caillol S, David G (2013) Biobased thermosetting epoxy: present and future. Chem Rev 114(2):1082–111510.1021/cr3001274 ↗
9. Ma S, Liu X, Fan L (2014) Synthesis and properties of a bio-based epoxy resin with high epoxy value and low viscosity. Chemsuschem 7(2):555–56210.1002/cssc.201300749 ↗
10. Ma S, Liu X, Jiang Y (2013) Bio-based epoxy resin from itaconic acid and its composites cured with anhydride and comonomers. Green Chem 15(1):245–25410.1039/C2GC36715G ↗
11. Maiorana A, Spinella S, Gross R-A (2015) Bio-based alternative to the diglycidyl ether of bisphenol A with controlled materials properties. Biomacromol 16(3):1021–103110.1021/acs.biomac.5b00014 ↗
12. Flint S, Markle T, Thompson S (2012) Bisphenol A exposure, effects, and policy: a wildlife perspective. J Environ Manag 104:19–3410.1016/j.jenvman.2012.03.021 ↗
13. Jiang H, Sun L, Zhang Y (2018) Estrogenic activity research of a novel fluorinated bisphenol and preparation of an epoxy resin as alternative to bisphenol a epoxy resin. Eur Polym J 108:507–51610.1016/j.eurpolymj.2018.09.020 ↗
14. Yang G, Rohde B-J, Tesefay H (2016) Biorenewable epoxy resins derived from plant-based phenolic acids. ACS Sustain Chem/Eng 4(12):6524–653310.1021/acssuschemeng.6b01343 ↗
15. Ma Q, Liu X, Zhang R (2013) Synthesis and properties of full bio-based thermosetting resins from rosin acid and soybean oil: the role of rosin acid derivatives. Green Chem 15(5):1300–131010.1039/c3gc00095h ↗
16. Nouailhas H, Aouf C, Le Guernevé C (2011) Synthesis and properties of biobased epoxy resins. Part 1. Glycidylation of flavonoids by epichlorohydrin. J Polym Sci Part A Polym Chem 49(10):2261–227010.1002/pola.24659 ↗
17. Huang K, Liu Z, Zhang J (2014) Epoxy monomers derived from tung oil fatty acids and its regulable composites cured in two synergistic ways. Biomacromol 15(3):837–84310.1021/bm4018929 ↗
18. Pan X, Sengupta P, Webster D-C (2011) Novel biobased epoxy compounds: epoxidized sucrose esters of fatty acids. Green Chem 13(4):965–97510.1039/c0gc00882f ↗
19. Kristufek SL, Yang G, Link LA (2016) Synthesis, characterization, and cross-linking strategy of a quercetin-based epoxidized monomer as a naturally-derived replacement for BPA in epoxy resins. Chemsuschem 9(16):2135–214210.1002/cssc.201600392 ↗
20. Rajan VK, Muraleedharan K (2017) A computational investigation on the structure, global parameters and antioxidant capacity of a polyphenol, Gallic acid. Food chem 220:93–9910.1016/j.foodchem.2016.09.178 ↗
21. Aouf C, Nouailhas H, Fache M (2013) Multi-functionalization of gallic acid. Synthesis of a novel bio-based epoxy resin. Eur Polym J 49(6):1185–119510.1016/j.eurpolymj.2012.11.025 ↗
22. Xu J, Yang J, Wang H (2019) Bio-based hyperbranched toughener from tannic acid and its enhanced solvent-free epoxy resin with high performance. J Renew Mater 7(12):1333–134610.32604/jrm.2019.07905 ↗
23. Ma S, Liu X, Jiang Y (2013) Bio-based epoxy resin from itaconic acid and its thermosets cured with anhydride and comonomers. Green Chem 15(1):245–25410.1039/C2GC36715G ↗
24. Shibata M, Enjoji M, Sakazume K (2016) Bio-based epoxy/chitin nanofiber composites cured with amine-type hardeners containing chitosan. Carbohydr polym 144:89–9710.1016/j.carbpol.2016.02.033 ↗
25. Liu T, Nie Y, Chen R (2015) Hyperbranched polyether as an all-purpose epoxy modifier: controlled synthesis and toughening mechanisms. J Mater Chem A 3(3):1188–119810.1039/C4TA04841E ↗
26. Xiao L, Liu Z, Hu F (2019) A renewable tung oil-derived nitrile rubber and its potential use in epoxy-toughening modifiers. Rsc Adv 9(44):25880–2588910.1039/C9RA01918A ↗
27. Kumar S, Samal SK, Mohanty S (2018) Recent development of biobased epoxy resins: a review. Polym-Plast Technol Eng 57(3):133–15510.1080/03602559.2016.1253742 ↗
28. Boro U, Karak N (2017) Tannic acid based hyperbranched epoxy/reduced graphene oxide nanocomposites as surface coating materials. Prog Org Coat 104:180–18710.1016/j.porgcoat.2016.10.039 ↗
29. Rivero S, Garcia MA, Pinotti A (2010) Crosslinking capacity of tannic acid in plasticized chitosan films. Carbohyd Polym 82(2):270–27610.1016/j.carbpol.2010.04.048 ↗
30. Fei X, Wei W, Zhao F (2017) Efficient toughening of epoxy–anhydride thermosets with a biobased tannic acid derivative[J]. ACS Sustain Chem/Eng 5(1):596–60310.1021/acssuschemeng.6b01967 ↗
31. Li L, Liao X, Sheng X (2019) Effect of structure regulation of hyper-branched polyester modified carbon nanotubes on toughening performance of epoxy/carbon nanotube nanocomposites. Rsc Adv 9(23):12864–1287610.1039/C9RA01550G ↗
32. Shibata M, Teramoto N, Makino K (2011) Preparation and properties of biocomposites composed of epoxidized soybean oil, tannic acid, and microfibrillated cellulose. J Appl Polym Sci 120(1):273–27810.1002/app.33082 ↗
33. Shibata M, Nakai K (2010) Preparation and properties of biocomposites composed of bio-based epoxy resin, tannic acid, and microfibrillated cellulose. J Polym Sci Part B Polym Phys 48(4):425–43310.1002/polb.21903 ↗
34. Fei X, Zhao F, Wei W (2016) Tannic acid as a bio-based modifier of epoxy/anhydride composites. Polymers 8(9):31410.3390/polym8090314 ↗
35. Patil D-M, Phalak G-A, Mhaske S-T (2017) Synthesis of bio-based epoxy resin from gallic acid with various epoxy equivalent weights and its effects on coating properties. J Coat Technol Res 14(2):355–36510.1007/s11998-016-9853-x ↗
36. Bagheri R, Marouf B-T, Pearson R-A (2009) Rubber-toughened epoxies: a critical review. Polym Rev 49(3):201–22510.1080/15583720903048227 ↗
37. Luo L, Meng Y, Qiu T (2013) An epoxy-ended hyperbranched polymer as a new modifier for toughening and reinforcing in epoxy resin. J Appl Polym Sci 130(2):1064–107310.1002/app.39257 ↗
38. Liu W, Zhou R, Goh H-L-S (2014) From waste to functional additive: toughening epoxy resin with lignin. ACS Appl Mater Inter 6(8):5810–581710.1021/am500642n ↗
39. Huang D-D, Xu F, Du X-S (2017) Temperature effects on rigid nano-silica and soft nano-rubber toughening in epoxy under impact loading. J Appl Polym Sci 134(38):4531910.1002/app.45319 ↗
40. Lv J, Meng Y, He L (2013) Novel epoxidized hyperbranched poly (phenylene oxide): synthesis and application as a modifier for diglycidyl ether of bisphenol A. J Appl Polym Sci 128(1):907–91410.1002/app.38270 ↗
41. Liu Y, Ramirez C, Zhang L (2017) In situ direct observation of toughening in isotropic nanocomposites of alumina ceramic and multiwall carbon nanotubes. Acta Mater 127:203–21010.1016/j.actamat.2017.01.024 ↗
42. Xu J, Yang J, Liu X (2018) Preparation and characterization of fast-curing powder epoxy adhesive at middle temperature. Roy Soc Open Sci 5(8):18056610.1098/rsos.180566 ↗
43. Zhang D, Zhang X, Jing T (2019) Tunable thermal, mechanical, and controlled-release properties of epoxy phenolic novolac resin microcapsules mediated by diamine crosslinkers. Rsc Adv 9(17):9820–982710.1039/C9RA00069K ↗
44. Kissinger H-E (1957) Reaction kinetics in different thermal analysis. Anal Chem 29:1702–170610.1021/ac60131a045 ↗
45. Ozawa T (1965) New method of analyzing thermogravimetric data. Bull Chem Soc Jpn 38:1881–188610.1246/bcsj.38.1881 ↗
46. Wang F, Kuai J, Pan H (2018) Study on the demethylation of enzymatic hydrolysis lignin and the properties of lignin–epoxy resin blends. Wood Sci Technol 52(5):1343–135710.1007/s00226-018-1024-z ↗
47. Shang L, Zhang X, Zhang M (2018) A highly active bio-based epoxy resin with multi-functional group: synthesis, characterization, curing and properties. J Mater Sci 53(7):5402–541710.1007/s10853-017-1797-8 ↗
48. Thanki J-D, Parsania P-H (2017) Dynamic DSC curing kinetics and thermogravimetric study of epoxy resin of 9, 9′-bis (4-hydroxyphenyl) anthrone-10. J Therml Anal Calorim 130(3):2145–2156. https://doi.org/10.1007/s10973-017-6761-y10.1007/s10973-017-6761-y ↗
49. Kumar S, Samal SK, Mohanty S (2019) Curing kinetics of bio-based epoxy resin-toughened DGEBA epoxy resin blend. J Therm Anal Calorim 137(5):1567–157810.1007/s10973-019-08080-4 ↗
50. Fei X, Wei W, Zhao F (2017) Efficient toughening of epoxy–anhydride thermosets with a biobased tannic acid derivative. ACS Sustain Chem/ Eng 5(1):596–60310.1021/acssuschemeng.6b01967 ↗