Reusable Polyphenol Building Blocks Enable Recyclable Epoxy-Amine Thermosets via Methanolysis
Yi-Min Tu1, Yuhang Jiang1, Kun Li2
1Institute of Chemistry and Biochemistry, Freie Universität Berlin, Berlin, Germany.
Abstract:
Biobased polyphenols represent attractive alternatives to bisphenol A for epoxy thermosets, yet most bio-derived epoxy networks remain permanently cross-linked and are difficult to recycle. Herein, we report a modular molecular design strategy that converts renewable polyphenols into reusable functional building blocks for recyclable epoxy-amine thermosets. Distinct from conventional degradable epoxy networks, this platform enables systematic structural variation and establishes a clear structure-depolymerization relationship. Kinetic and computational analyses further support a previously unrecognized ether-assisted methanolysis mechanism, in which neighboring ether functionalities and a favorable aliphatic amine environment lower the apparent kinetic barrier and modulate the local methanol environment around the cleavable ester bonds in a configuration-dependent manner. Consequently, the resulting thermosets undergo efficient methanolysis under mild conditions (70°C), affording reusable molecular components while maintaining tunable thermal and mechanical properties. Furthermore, carbon fiber-reinforced composites based on the optimized formulation can be efficiently depolymerized, yielding intact fibers and reusable building blocks in 88% isolated yield. The recovered polyols can be further upcycled into antibacterial quaternary ammonium materials, demonstrating a value-added reuse pathway. This work identifies a previously unrecognized molecular promotion mechanism for catalyst-free methanolysis and translates this mechanism insight into a structural design principle for recyclable polyphenol-based epoxy-amine thermosets.
Related Concept Videos
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Types of Step-Growth Polymers: Polyesters
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the polymer...
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more substituted...


