Du Yuetian, Wang Dong
State Key Laboratory of Organic-Inorganic Composites & Beijing Key Laboratory of Advanced Functional Polymer Composites, Beijing University of Chemical Technology, Beijing 100029, China.
ACS Appl Mater Interfaces. 2024 Aug 7;16(31):41551-41561. doi: 10.1021/acsami.4c09123. Epub 2024 Jul 23.
Although considerable progress has been made in developing different types of vitrimers, ongoing challenges remain in tuning their mechanical and rheological properties, self-healing, and adhesion. Here, we demonstrate a one-pot method to produce a novel double-network epoxy vitrimer using an aliphatic amine cross-linker with a siloxane covalent bond and an aromatic amine cross-linker with a disulfide covalent bond. When a controlled two-stage curing process is employed, the markedly different reactivities of aliphatic amine and aromatic amine with epoxy allow for sequential cross-linked network formation, leading to the development of a double network that incorporates two types of dynamic covalent bonds. As a result, the produced vitrimers exhibit controllable mechanical, thermal, and rheological properties, as well as recyclability. This is evidenced by a tensile strength as high as 72 MPa, while maintaining ∼10% elongation at break, a wide glass-transition temperature range from 91 to 171 °C, and an adjustable two-stage stress relaxation. These characteristics suggest opportunities to develop high-performance cross-linked polymers with specific responses to time and temperatures.
尽管在开发不同类型的玻璃态物质方面已经取得了相当大的进展,但在调节它们的机械和流变性能、自愈性能及粘附性方面仍存在持续的挑战。在此,我们展示了一种一锅法,使用具有硅氧烷共价键的脂肪族胺交联剂和具有二硫键共价键的芳香族胺交联剂来制备一种新型的双网络环氧玻璃态物质。当采用可控的两步固化过程时,脂肪族胺和芳香族胺与环氧树脂明显不同的反应活性允许依次形成交联网络,从而形成包含两种类型动态共价键的双网络。结果,所制备的玻璃态物质表现出可控的机械、热和流变性能以及可回收性。这通过高达72 MPa的拉伸强度得到证明,同时保持约10%的断裂伸长率、91至171 °C的宽玻璃化转变温度范围以及可调节的两步应力松弛来体现。这些特性为开发对时间和温度具有特定响应的高性能交联聚合物提供了机会。