Simultaneous Enhanced Mechanical Properties and Foamability of Biodegradable PBAT via Physical Cross-Linking through Reactive Blending
While fully biodegradable poly(butylene adipate-co-terephthalate) (PBAT) is considered to be one of the most promising materials, the application of PBAT materials is still hindered due to its intrinsic low mechanical strength and poor foamability. Herein, a strategy is addressed to construct PBAT-based supramolecular bionanocomposites of high strength and excellent foamability with homogeneous dispersion of UPy aggregates via quadruple hydrogen bonding. The biocomposite was prepared by direct melt-blending of isocyanate-terminal ureido-pyrimidinone (UPy-NCO) and PBAT. It was found that the terminal hydroxyl group of PBAT quickly reacted with the isocyanate group of UPy-NCO during the mixing and in-situ formed a dimerized supramolecular polymer (PBAT-UPy-UPy-PBAT) owing to quadruple hydrogen bonding. The PBAT-UPy-UPy-PBAT could be further folded via longitudinal hydrogen-bonding interactions between the ureido groups of UPy units, forming ordered needle-like UPy nanoassemblies in the PBAT matrix. Such particular nanoassemblies could function as physical cross-linking points for PBAT-based composites, resulting in simultaneous improved mechanical strength and foamability of PBAT. This work paves a feasible avenue for manufacturing high-performance PBAT biocomposites and corresponding foams, which is challenging in existing industrial technologies.
Authors
- Xiayan Ling
- Hengti Wang (ORCID: https://orcid.org/0000-0003-1650-0651)
- Yongjin Li (ORCID: https://orcid.org/0000-0001-6666-1336)
- Xin Yang (ORCID: https://orcid.org/0000-0003-1819-3261)
Institutions
- Hangzhou Normal University (CN)
Publication Details
- Journal
- ACS Applied Polymer Materials
- Published
- 2024-11-06
- DOI
- https://doi.org/10.1021/acsapm.4c03104
- Citations
- 4
- Primary Topic
- biodegradable polymer synthesis and properties
- Type
- article
- Field-Weighted Citation Impact
- 0.69
Funders
- National Natural Science Foundation of China