Abstract

In the recent years, generation of flexible, mechanically tough, shape memory (SM) polymers has gained a remarkable significance both in academic section and in the field of soft robotics, smart textiles, self-deployable structures (especially used in aerospace), actuators, bio-medical devices and so on. But designing of such materials poses a credible challenge to researchers in the field. Hence, in this work, we develop a bis(hydroxyalkyl)-poly(dimethylsiloxane) capped-(3-aminopropyl)trimethoxysilane functionalized-hydroxy iron oxide anchored-reduced graphene oxide nanohybrid which serves as a reinforcing agent for the generation of nanocomposites with SM, self-tightening and hydrophobic attributes. The prepared polystyrene/thermoplastic polyurethane (PS/TPU) interpenetrating network (IPN) nanocomposites recover their original shape at a faster rate (within 20–40s upon thermal heating and within 100–140s upon exposure to sunlight) compared to other similar type SM materials (require h to min). Moreover, the nanocomposites also showed thermally actuated artificial muscle-like and self-tightening behaviors. In addition, the nanocomposite containing 1 wt% nanohybrid demonstrated >200% increase in tensile strength, >120% increase in initial thermal degradation temperature, and strong surface hydrophobicity (static contact angle >120°). Therefore, the reported nanocomposites have considerable prospect for different smart applications.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.