材料科学
硅氧烷
自愈
超分子聚合物
自愈材料
无定形固体
复合材料
共价键
聚二甲基硅氧烷
涂层
应力松弛
超分子化学
纳米技术
化学工程
聚合物
有机化学
分子
蠕动
工程类
病理
替代医学
医学
化学
作者
Dijwar Yilmaz,Mickaël Du Fraysseix,Simon Lewandowski,Sophie Perraud,Emmanuel Ibarboure,Audrey Llevot,Stéphane Carlotti
标识
DOI:10.1021/acsami.4c02431
摘要
When exposed to the geostationary orbit, polymeric materials tend to degrade on their surface due to the appearance of cracks. Implementing the self-healing concept in polymers going to space is a new approach to enhancing the lifespan of materials that cannot be replaced once launched. In this study, the elaboration of autonomous self-healing transparent poly(dimethylsiloxane) (PDMS) materials resistant to proton particles is presented. The PDMS materials are functionalized with various compositions of urea and imine moieties, forming dynamic covalent and/or supramolecular networks. The hydrogen bonds induced by the urea ensure the formation of a supramolecular network, while the dynamic covalent imine bonds are capable of undergoing exchange reactions. Materials with a broad range of mechanical properties were obtained depending on the composition and structure of the PDMS networks. As coating applications in a spatial environment were mainly targeted, the surface properties of the polymer are essential. Thus, percentages of scratch recovery were determined by AFM. From these data, self-healing kinetics were extracted and rationalized based on the polymer structures. The obtained data were in good agreement with the relaxation times determined by rheology in stress relaxation experiments. Moreover, the accelerated aging of materials under proton irradiation, simulating a major part of the geostationary environment, revealed a strong limitation or disappearance of cracks while keeping the transparency of the PDMS. These promising results open routes to prepare new flexible autonomous polymeric materials for space applications.
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