Recyclable and Self-Healing Polyurethane Vitrimers via Dynamic Bonding with In-Situ Polymerized PHPMA

6Citations
Citations of this article
21Readers
Mendeley users who have this article in their library.

Abstract

The development of lightweight, durable, and recyclable polymer materials with self-healing properties remains a significant challenge in materials science, particularly for applications requiring extended service life and sustainability. This study addresses these challenges by introducing a novel thermoplastic polyurethane (PU)-based vitrimer system, synthesized via in situ polymerization using hydroxypropyl methacrylate (HPMA)-hydroxyl precursor and Tin(II) 2-ethylhexanoate (Sn(Oct)2)-catalyst. Unlike conventional vitrimer systems, this approach leverages dynamic bond exchange reactions without the formation of new covalent bonds, ensuring efficient stress relaxation and recyclability. Notably, the PU-PHPMA-73-Sn(Oct)2 composition exhibited superior mechanical properties and maintained its performance after three recycling cycles, highlighting its durability and circular potential. Stress relaxation studies further confirmed the temperature-dependent bond exchange kinetics, with activation energies of 122.8±8.1 kJ/mol and 21.6±2.4 kJ/mol for different compositions, correlating with the hydroxyl content. The vitrimer also demonstrated an 88.5 % self-healing efficiency, showcasing its ability to autonomously repair damage and extend material lifespan. This lightweight, self-healing, thermally stable, and recyclable vitrimer system presents significant advancements over traditional PU-based materials, with promising applications in medical devices, automotive components, adhesives, and advanced coatings, particularly where longevity and sustainability are critical.

Cite

CITATION STYLE

APA

Ghosh, S., Koley, S., Maiti, M., & Maji, P. K. (2025). Recyclable and Self-Healing Polyurethane Vitrimers via Dynamic Bonding with In-Situ Polymerized PHPMA. Chemistry - An Asian Journal, 20(6). https://doi.org/10.1002/asia.202401174

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free