Unraveling a path for multi-cycle recycling of tailored fiber-reinforced vitrimer composites

被引:13
|
作者
Zhou, Zhengping [1 ]
Kim, Sungjin [1 ]
Bowland, Christopher C. [1 ]
Li, Bingrui [1 ,4 ]
Ghezawi, Natasha [1 ,4 ]
Lara-Curzio, Edgar [2 ]
Hassen, Ahmed [3 ]
Naskar, Amit K. [1 ]
Rahman, Md Anisur [1 ]
Saito, Tomonori [1 ]
机构
[1] Oak Ridge Natl Lab, Chem Sci Div, Phys Sci Directorate, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Mat Sci & Technol Div, Oak Ridge, TN 37831 USA
[3] Mfg Sci Div, Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
[4] Univ Tennessee Knoxville, Bredesen Ctr Interdisciplinary Res & Educ, Knoxville, TN 37966 USA
来源
CELL REPORTS PHYSICAL SCIENCE | 2022年 / 3卷 / 09期
关键词
EPOXY VITRIMER; HIGH-PERFORMANCE; PLASTICS; TEMPERATURE; THERMOSETS; TRANSESTERIFICATION;
D O I
10.1016/j.xcrp.2022.101036
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Manufacturing transformation toward a net-zero carbon society demands polymeric composite materials to be reprocessable in circularity in an energy-efficient and stable manner. Recent advancements in vitrimers have bestowed crosslinked polymers like epoxies with reprocessability, opening a path for the circular manufacturing of thermosets. However, (re)processing of mechanically robust vitrimers such as epoxy vitrimers typically requires high temperatures and long processing times, which cause degradation and compromise efficient recyclability. Here, we report a simple design of dynamic polyurea/epoxy (DPE) vitrimers and their carbon-fiber-reinforced polymers (CFRPs) with exchangeable disulfide crosslinks, which overcome such intrinsic limitations. Compared with conventional epoxy vitrimers, the DPE vitrimer exhibits 6 times faster bond rearrangement and similar to 40 degrees C lower reprocessing temperature, which enables full recovery of the mechanical strength throughout 6 reprocessing cycles, while the conventional vitrimer lost similar to 63% of strength. Moreover, the CFRPs prepared with the DPE vitrimers exhibit facile multi-cycle processability and repairability by thermoformation.
引用
收藏
页数:16
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