Felsenthal Lillian M, Kim Subeen, Dichtel William R
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States.
ACS Appl Mater Interfaces. 2024 Oct 23;16(42):57687-57694. doi: 10.1021/acsami.4c12415. Epub 2024 Oct 15.
Thermoset polyurethanes (PUs) have been successfully reprocessed as covalent adaptable networks (CANs) by catalyzing carbamate exchange. Here we extend bond exchange beyond the internal network cross-links to create a dynamic urethane adhesive. Interfacing PU CANs to substrates with nucleophilic functional groups creates adhesives capable of reversible transcarbamoylation with the substrate, which has not been demonstrated previously by CAN adhesives. Two types of thermoset PU films were synthesized, one containing the green carbamate exchange catalyst Zr(tmhd) and the other containing no catalyst. Although otherwise identical in chemical and network properties, as indicated by FT-IR spectroscopy and dynamic mechanical thermal analysis (DMTA), the film containing catalyst showed dynamic bond exchange behavior through stress relaxation analysis. When evaluated as an adhesive, the CAN film exhibited self-healing properties and retained its adhesive strength for five cycles, which is attributed to reversible covalent bonding to the glass substrate. This work expands industrially relevant CANs to structural adhesives and demonstrates their potential value in an application that presently employs PUs as single-use materials.
热固性聚氨酯(PU)已通过催化氨基甲酸酯交换成功地作为共价适应性网络(CAN)进行再加工。在此,我们将键交换扩展到内部网络交联之外,以创建一种动态聚氨酯粘合剂。将PU CAN与具有亲核官能团的基材连接,可形成能够与基材进行可逆氨基甲酰化反应的粘合剂,这是CAN粘合剂以前未曾证明过的。合成了两种类型的热固性PU薄膜,一种含有绿色氨基甲酸酯交换催化剂Zr(tmhd),另一种不含催化剂。尽管通过傅里叶变换红外光谱(FT-IR)和动态机械热分析(DMTA)表明,它们在化学和网络性质上其他方面相同,但含有催化剂的薄膜通过应力松弛分析显示出动态键交换行为。当作为粘合剂进行评估时,CAN薄膜表现出自愈性能,并在五个循环中保持其粘合强度,这归因于与玻璃基材的可逆共价键合。这项工作将工业相关的CAN扩展到结构粘合剂,并证明了它们在目前将PU用作一次性材料的应用中的潜在价值。