journal article·2024-01-26

Solvent-Free and Recyclable Polyether/Polyphenol Supramolecular Adhesives with Robust, Water- and Low-Temperature-Resistant Properties

Xianqiang Zeng, Liguo Wang, Yan Cao, Peng He, Xiaoxuan Wang, Huiquan Li

ACS Applied Polymer Materials· Volume 6· Issue 2
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Abstract

Adhesives are widely used in everyday life; however, traditional polymer adhesives pose unavoidable hazards to the environment and living organisms due to their extensive use of toxic organic solvents, heavy reliance on fossil resources as synthetic raw materials, and lack of recyclability. Furthermore, they are incapable of maintaining a stable adhesion performance in harsh conditions. In this work, we present a facile yet powerful noncovalent bonding strategy for successfully constructing poly(glycidol- co -1,2-butylene oxide)/tannic acid supramolecular adhesives (PG- co -PBO/TA SAs) through hydrogen-bonding interactions between hyperbranched PG- co -PBO and natural TA. The SAs demonstrate an adhesion strength of 2.15 MPa at ambient temperature and maintain an adhesion strength of 1.53 MPa even at −196 °C. Moreover, it can be easily recycled through thermal treatment and retains stable adhesion strength even after undergoing multiple recycling cycles. The investigation of the structure–property relationship of SAs and molecular dynamics simulations has clarified that short alkyl chains of PG- co -PBO effectively protect the hydrogen-bonding networks from damage by repelling water at the adhesive interface. Consequently, SAs even maintain robust and long-lasting adhesion strength in acidic, alkaline, and seawater solutions. Importantly, unlike conventional adhesives, SAs do not employ organic solvents throughout the synthesis, bonding, and recycling processes. By designing functionalized polymers and utilizing polyphenolic compounds, this work provides a green and feasible strategy for the development of next-generation powerful supramolecular adhesives.
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Research context

OpenAlex topics: Advanced Polymer Synthesis and Characterization · Synthesis and properties of polymers · biodegradable polymer synthesis and properties

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

Affiliations

School of Chemistry and Chemical Engineering, Nanchang University, Nanchang 330031, China

Ganjiang Innovation Academy, Chinese Academy of Sciences, Ganzhou 341000, China

CAS Key Laboratory of Green Process and Engineering, National Engineering Research Center of Green Recycling for Strategic Metal Resources, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China

Sino-Danish Center for Education and Research, University of Chinese Academy of Sciences, Beijing 100049, China

School of Chemical Engineering, University of Chinese Academy of Sciences, Beijing 100049, China

Funding

National Key Research and Development Program of China · Science and Technology Major Project of Inner Mongolia · Chinese Academy of Sciences · Clean Combustion and Low-carbon Utilization of Coal

References (47)

Show source-provided references
1. 10.1039/D2GC01637K10.1039/D2GC01637K ↗
2. 10.1016/j.carbpol.2017.12.01910.1016/j.carbpol.2017.12.019 ↗
3. 10.1002/adfm.20230410110.1002/adfm.202304101 ↗
4. 10.1002/adfm.20180080210.1002/adfm.201800802 ↗
5. Xu, R.; Yin, C.; You, J.; Zhang, J.; Mi, Q.; Wu, J.; Zhang, J.Sustainable, Thermoplastic and Hydrophobic Coating from Natural Cellulose and Cinnamon to Fabricate Eco-Friendly Catering Packaging Green Energy Environ. 2022 10.1016/j.gee.2022.10.009.10.1016/j.gee.2022.10.009 ↗
6. 10.1002/adfm.20220730610.1002/adfm.202207306 ↗
7. 10.1002/adfm.20221134010.1002/adfm.202211340 ↗
8. 10.1002/adfm.20220559710.1002/adfm.202205597 ↗
9. 10.1016/j.apsusc.2019.14424610.1016/j.apsusc.2019.144246 ↗
10. 10.1002/adfm.20190855810.1002/adfm.201908558 ↗
11. 10.1016/j.porgcoat.2021.10669210.1016/j.porgcoat.2021.106692 ↗
12. 10.1002/anie.20130276610.1002/anie.201302766 ↗
13. 10.1039/D1GC03306A10.1039/D1GC03306A ↗
14. 10.1039/D3GC01253K10.1039/D3GC01253K ↗
15. 10.1126/science.aac817410.1126/science.aac8174 ↗
16. 10.1021/acscentsci.8b0052610.1021/acscentsci.8b00526 ↗
17. 10.1021/ma201044x10.1021/ma201044x ↗
18. 10.1002/macp.20220033210.1002/macp.202200332 ↗
19. 10.1002/anie.20230350610.1002/anie.202303506 ↗
20. 10.1002/advs.20220318210.1002/advs.202203182 ↗
21. 10.1002/advs.20220026410.1002/advs.202200264 ↗
22. 10.1002/adom.20190023010.1002/adom.201900230 ↗
23. 10.1016/j.cej.2021.13384010.1016/j.cej.2021.133840 ↗
24. 10.1002/adma.20210606710.1002/adma.202106067 ↗
25. 10.1002/anie.20220387610.1002/anie.202203876 ↗
26. 10.1021/acsmaterialslett.3c0072810.1021/acsmaterialslett.3c00728 ↗
27. 10.1021/jacs.0c0052010.1021/jacs.0c00520 ↗
28. 10.1002/anie.20220742510.1002/anie.202207425 ↗
29. 10.1039/D1RA07657D10.1039/D1RA07657D ↗
30. 10.1002/adfm.20150003410.1002/adfm.201500034 ↗
31. 10.1021/acsami.1c0134310.1021/acsami.1c01343 ↗
32. 10.1021/acsami.0c0203710.1021/acsami.0c02037 ↗
33. 10.1021/acsami.6b0837410.1021/acsami.6b08374 ↗
34. 10.1002/app.4828510.1002/app.48285 ↗
35. 10.1021/acs.biomac.2c0022310.1021/acs.biomac.2c00223 ↗
36. 10.1021/acs.macromol.9b0030210.1021/acs.macromol.9b00302 ↗
37. 10.1016/j.polymer.2012.07.04710.1016/j.polymer.2012.07.047 ↗
38. 10.1016/j.eurpolymj.2022.11148310.1016/j.eurpolymj.2022.111483 ↗
39. 10.1016/j.cej.2020.12706910.1016/j.cej.2020.127069 ↗
40. 10.1021/acs.macromol.6b0210610.1021/acs.macromol.6b02106 ↗
41. 10.1021/acsami.2c0023610.1021/acsami.2c00236 ↗
42. 10.1002/marc.20210083010.1002/marc.202100830 ↗
43. 10.1016/j.cej.2021.13225210.1016/j.cej.2021.132252 ↗
44. 10.1016/j.jcis.2022.11.01710.1016/j.jcis.2022.11.017 ↗
45. 10.1021/jacs.9b0267710.1021/jacs.9b02677 ↗
46. 10.1038/ncomms1591110.1038/ncomms15911 ↗
47. 10.1002/adfm.20170419510.1002/adfm.201704195 ↗