Synthesis of Polybenzoxazine as an environmentally friendly adhesive material from cardanol and post-consumer PET source
Author affiliations
DOI:
https://doi.org/10.15625/2525-2518/18526Keywords:
Cardanol, benzoxazine, post-consumer Polyethylene terephthalate, adhesiveAbstract
In this study, a thermosetting benzoxazine was successfully prepared from environmentally friendly sources to be used as an adhesive. The phenolic component used for the synthesis of the benzoxazine monomer is cardanol derived from the cashew nutshell, while the amine fractions are terephthalamide, which is a product of the amination process of used polyethylene terephthalate plastic bottles (PET). The structure of the benzoxazine monomer was determined by FT-IR and 1H-NMR spectroscopy. The thermal and curing behavior of the materials was investigated by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). A lap-shear adhesion testing (ASTM D1002-10) was performed to measure the bond strength of the material to the CT3 steel surface. The adhesive properties with a shear strength of 7.29 MPa are excellent compared to other commercial adhesives. This result indicates the great potential of this benzoxazine for adhesive applications in practice.
Downloads
References
Kinloch, A. J.; Kinloch, A. J., Adhesion and adhesives: science and technology. Springer Science & Business Media: 1987. DOI: https://doi.org/10.1007/978-94-015-7764-9
Banea, M. D.; da Silva, L. F.; Campilho, R. D.; Sato, C., Smart adhesive joints: An overview of recent developments. The Journal of Adhesion 2014, 90 (1), 16-40. https://doi.org/10.1080/00218464.2013.785916 DOI: https://doi.org/10.1080/00218464.2013.785916
Onusseit, H.; Wefringhaus, R.; Dreezen, G.; Wichelhaus, J.; Schall, J.; Thiele, L.; van Halteren, A., Adhesives, 1. general. Ullmann's Encyclopedia of Industrial Chemistry 2010, 440-481. https://doi.org/10.1002/14356007.a01_221.pub3 DOI: https://doi.org/10.1002/14356007.a01_221.pub3
Van, K. N., Chemical and technological adhesive. Publisher of Vietnam Academy of Science and Technology 2006.
Schmidt, R. G.; Bell, J. P., Epoxy adhesion to metals. Epoxy resins composites II 2005, 33-71. DOI: https://doi.org/10.1007/BFb0017914
Nečasová, B.; Liška, P.; Kelar, J.; Šlanhof, J., Comparison of adhesive properties of polyurethane adhesive system and wood-plastic composites with different polymers after mechanical, chemical and physical surface treatment. Polymers 2019, 11 (3), 397. https://doi.org/10.3390/polym11030397 DOI: https://doi.org/10.3390/polym11030397
Leggat, P. A.; Smith, D. R.; Kedjarune, U., Surgical applications of cyanoacrylate adhesives: a review of toxicity. ANZ journal of surgery 2007, 77 (4), 209-213. https://doi.org/10.1111/j.1445-2197.2007.04020.x DOI: https://doi.org/10.1111/j.1445-2197.2007.04020.x
Sharma, P.; Lochab, B.; Kumar, D.; Roy, P. K., Sustainable bis-benzoxazines from cardanol and PET-derived terephthalamides. ACS Sustainable Chemistry & Engineering 2016, 4 (3), 1085-1093. https://doi.org/10.1021/acssuschemeng.5b01153 DOI: https://doi.org/10.1021/acssuschemeng.5b01153
Voirin, C.; Caillol, S.; Sadavarte, N. V.; Tawade, B. V.; Boutevin, B.; Wadgaonkar, P. P., Functionalization of cardanol: towards biobased polymers and additives. Polymer Chemistry 2014, 5 (9), 3142-3162. https://doi.org/10.1039/C3PY01194A DOI: https://doi.org/10.1039/C3PY01194A
Mohapatra, S.; Nando, G. B., Cardanol: a green substitute for aromatic oil as a plasticizer in natural rubber. Rsc Advances 2014, 4 (30), 15406-15418. https://doi.org/10.1039/C3RA46061D DOI: https://doi.org/10.1039/C3RA46061D
A Attanasi, O.; S Behalo, M.; Favi, G.; Lomonaco, D.; E Mazzetto, S.; Mele, G.; Pio, I.; Vasapollo, G., Solvent free synthesis of novel mono-and bis-benzoxazines from cashew nut shell liquid components. Current Organic Chemistry 2012, 16 (21), 2613-2621. https://doi.org/10.2174/138527212804004616 DOI: https://doi.org/10.2174/138527212804004616
Wang, X.; Yu, L.; Liu, Y.; Jiang, X., Synthesis and fouling resistance of capsaicin derivatives containing amide groups. Science of The Total Environment 2020, 710, 136361. https://doi.org/10.1016/j.scitotenv.2019.136361 DOI: https://doi.org/10.1016/j.scitotenv.2019.136361
Hoang, C. N.; Dang, Y. H., Aminolysis of poly (ethylene terephthalate) waste with ethylenediamine and characterization of α, ω-diamine products. Polymer degradation and stability 2013, 98 (3), 697-708. https://doi.org/10.1016/j.polymdegradstab.2012.12.026 DOI: https://doi.org/10.1016/j.polymdegradstab.2012.12.026
Khan, M. M.; Halder, K.; Shishatskiy, S.; Filiz, V., Synthesis and crosslinking of polyether-based main chain benzoxazine polymers and their gas separation performance. Polymers 2018, 10 (2), 221. https://doi.org/10.3390/polym10020221 DOI: https://doi.org/10.3390/polym10020221
Tuong, H. K., Investigation of Benzoxazine resin derived from cardanol on the properties of natural rubber compounds. Thesis 2023, 28-34.
Downloads
Published
How to Cite
Issue
Section
License
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
Vietnam Journal of Sciences and Technology (VJST) is an open access and peer-reviewed journal. All academic publications could be made free to read and downloaded for everyone. In addition, articles are published under term of the Creative Commons Attribution-ShareAlike 4.0 International (CC BY-SA) Licence which permits use, distribution and reproduction in any medium, provided the original work is properly cited & ShareAlike terms followed.
Copyright on any research article published in VJST is retained by the respective author(s), without restrictions. Authors grant VAST Journals System a license to publish the article and identify itself as the original publisher. Upon author(s) by giving permission to VJST either via VJST journal portal or other channel to publish their research work in VJST agrees to all the terms and conditions of https://creativecommons.org/licenses/by-sa/4.0/ License and terms & condition set by VJST.
Authors have the responsibility of to secure all necessary copyright permissions for the use of 3rd-party materials in their manuscript.