Covalent adaptable networks through dynamic N,S-acetal chemistry: toward recyclable CO2-based thermosets

31 August 2023, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Designing easily recyclable polymers with customized properties is a key challenge to face up environmental concerns and the growing plastics demand. Here, we report a dynamic chemistry between CO2-sourced alkylidene oxazolidones and thiols that delivers circular non-isocyanate polyurethane networks embedding N,S-acetal bonds. Oxazolidones are synthesized from cheap reagents and carbon dioxide. The polymer structure is tuned by monomer design, translating in a wide panel of mechanical properties, ranging from PDMS-like elastomers (Young’s modulus (E) = 2.9 MPa and elongation at break (Ebreak) = 159%) to polystyrene-like rigid plastics (E = 2800 MPa, Ebreak = 2%). The dynamic nature of the N,S-acetal bond offers multiple closed- and open-loop recycling options, facilitating repeated thermoset reprocessing into the same material or the production of a different one of distinct properties. The versatility of this chemistry shows great potential for preparing materials (including composites) of tunable properties that can be recycled by multiple scenarios.

Keywords

recyclable thermoset
carbon dioxide valorization
covalent adaptable network
dynamic covalent chemistry
polyoxazolidone
polyurethane

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