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.