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September 8, 2026Macromolecular Rapid CommunicationsOpen Access

A Chemically Recyclable 1,3,5‐Triazine‐Based Epoxy Thermoset Enabled by Nucleophilic Aromatic Substitution Reaction

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Authors

YCYi‐Ru ChenFEFabian EisenreichAEA. Catarina C. Esteves

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Overview

Experimental study demonstrates closed-loop chemical recycling in high-performance 1,3,5-triazine epoxy thermosets, highlighting a viable pathway toward sustainable industrial polymers.

Key Points

  • Develop a high-performance, chemically recyclable epoxy thermoset utilizing nucleophilic aromatic substitution without sacrificing thermal and mechanical robustness.
  • Synthesized a cross-linked thermoset under bulk conditions using the trifunctional epoxy monomer TOMTA and secondary aromatic diamine hardener MBMA.
  • Conducted network depolymerization using an optimized binary K2CO3/TBD catalyst system in ethanol, followed by liquid-liquid extraction.
  • Characterized thermomechanical properties, evaluated recyclability across multiple closed-loop cycles, and demonstrated application as a debondable glass coating.
  • The synthesized thermoset exhibited a glass transition temperature (Tg) of 105°C, thermal degradation temperature (Td5%) of 256°C, Young's modulus of 3.0 GPa, and tensile strength of 96 MPa.
  • Catalyzed depolymerization recovered building blocks TETA and tetraol BDHPPM in 70% and 65% yields, respectively.
  • Re-crosslinking the recovered monomers fully regenerated the thermoset network with nearly identical mechanical properties across repeated recycling cycles.

Cite This Study

Chen et al. (2026) studied this question.

synapsesocial.com/papers/6a9fd82f58e84d0ff5b477e2https://doi.org/10.1002/marc.70422
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