Mah Justin Jian Qiang, Li Ke, Feng Hongzhi, Surat'man Nayli Erdeanna Binte, Li Bofan, Yu Xiaohui, Zhang Mingsheng, Wang Sheng, Li Zibiao
Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology and Research (A*STAR), 2 Fusionopolis Way, Innovis #08-03, Singapore, 138634, Republic of Singapore.
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, 637371, Republic of Singapore.
Chem Asian J. 2024 Jun 17;19(12):e202400143. doi: 10.1002/asia.202400143. Epub 2024 May 6.
The loss of function after prolonged periods of use is inevitable for all materials including plastics. Hence, self-healing capabilities are a key development to prolong the service lifetime of materials. One of such self-healing capabilities can be achieved by integrating dynamic bonds such as boronic ester linkages into polymeric materials, however the rate of self-healing in these materials is insufficient and current methods to accelerate it are limited. In this study, we report the rational design, synthesis and characterization of a fluorinated elastomer (FBE15) that utilizes enhanced interaction between polymer chains afforded by strong dipole-dipole interactions from -CF, which showed a significant increase in binding energy to -7.71 Kcal/mol from -5.51 Kcal/mol, resulting in increased interaction between the boronic ester linkages and improving self-healing capabilities of boronic ester materials, drastically reducing the time required for stress relaxation by 900 %. The bulk elastomer is capable of ultrafast self-healing in a one-click fashion that can happen in mere seconds, which can then be stretched to 150 % of its original length. By utilising the dynamic cross-linking, FBE15 is also capable of both mechanical reprocessing into the same materials and chemical recycling into its starting materials, respectively, further allowing reconstruction of the elastomers that have comparable properties to the original ones at the end of its service lifespan.
包括塑料在内的所有材料在长时间使用后功能丧失都是不可避免的。因此,自修复能力是延长材料使用寿命的关键发展方向。将硼酸酯键等动态键整合到聚合物材料中可以实现其中一种自修复能力,然而这些材料的自修复速率不足,目前加速自修复的方法也有限。在本研究中,我们报告了一种含氟弹性体(FBE15)的合理设计、合成与表征,该弹性体利用了由 -CF 产生的强偶极 - 偶极相互作用所提供的聚合物链间增强相互作用,其与硼酸酯键的结合能从 -5.51 千卡/摩尔显著增加至 -7.71 千卡/摩尔,从而增强了硼酸酯键之间的相互作用,提高了硼酸酯材料的自修复能力,使应力松弛所需时间大幅减少了900%。本体弹性体能够以一键式方式在短短几秒钟内实现超快自修复,然后可拉伸至其原始长度的150%。通过利用动态交联,FBE15还能够分别进行机械再加工成相同材料以及化学回收成起始材料,进一步使得在其使用寿命结束时能够重建出具有与原始材料相当性能的弹性体。