Phosphorus/boron-containing, flame-retardant polyurethane elastomers with great mechanical, shape-memory, and recycling performances
• A recyclable PU-DP 1–7 elastomer with dynamic borate acid esters was fabricated; • PU-DP 1–7 shows a UL-94 V-0 rating and an LOI of 24.8 %; • The tensile strength and elongation at break of PU-DP 1–7 reach 42.7 MPa and 616.9 %; • PU-DP 1–7 can be physically recycled at 130 and 140 °C; • PU-DP 1–7 has shape-memory properties. Based on sustainable development strategy and practical application requirement, it is crucial to develop high-strength, recyclable, and flame-retardant polyurethane (PU) elastomers. Hence, a flame-retardant, reprocessable, high-performance polyurethane elastomer (PU-DP 1–7) with dynamic boronic ester bonds and phosphorus-containing groups was well-designed and prepared. The chemical structure of PU-DP 1–7 was confirmed by Fourier transform infrared spectrometry (FTIR) and X-ray photoelectron spectroscopy (XPS). PU-DP 1–7 shows a transmittance of about 60 % at the wavelength of 900 nm, and phosphorus and boron elements are evenly distributed within its surface, confirming the formation of uniform cross-linking network. The inclusion of phosphorus-and boron-containing groups endows PU-DP 1–7 with a vertical combustion (UL-94) V-0 rating, indicative of desired flame retardancy. In addition, PU-DP 1–7 exhibits a tensile strength of 42.7 MPa and an elongation at break of 616.9 %, with high adhesion strengths towards various substrates due to abundant hydrogen bonds within its network. Furthermore, the dynamic borate ester bonds endow PU-DP 1–7 with superior physical recycling and shape-memory properties. After hot-pressing at 130 °C, the reformed PU-DP 1–7 film shows an 83.6 % recovery efficiency in terms of elongation at break. This work presents an integrated strategy to create flame-retardant, recyclable polyurethane elastomers with great mechanical and shape-memory performances by introducing phosphorus-containing segments and dynamic boronic ester bonds.
Authors
- Cheng Wang (ORCID: https://orcid.org/0000-0001-7653-3100)
- Guofeng Ye (ORCID: https://orcid.org/0000-0002-8217-5415)
- Siqi Huo (ORCID: https://orcid.org/0000-0002-6454-5208)
- Pingan Song (ORCID: https://orcid.org/0000-0003-1082-652X)
- Zhitian Liu (ORCID: https://orcid.org/0000-0001-5284-3358)
- Yijiao Xue (ORCID: https://orcid.org/0000-0003-4827-7976)
- Qi Zhang (ORCID: https://orcid.org/0000-0003-1940-8471)
- Tiantian Zhang (ORCID: https://orcid.org/0000-0002-5162-0408)
- Hao Wang (ORCID: https://orcid.org/0000-0001-7414-0426)
Institutions
- University of Southern Queensland (AU)
- Institute of Chemical Industry of Forest Products (CN)
- Chinese Academy of Forestry (CN)
- Wuhan Institute of Technology (CN)
Publication Details
- Journal
- Polymer Degradation and Stability
- Published
- 2024-10-19
- DOI
- https://doi.org/10.1016/j.polymdegradstab.2024.111047
- Citations
- 21
- Primary Topic
- Polymer composites and self-healing
- Type
- article
- Field-Weighted Citation Impact
- 3.54
Funders
- Australian Research Council