Related Experiment Video
Updated: Aug 12, 2025

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene
Published on: May 20, 2019
Depolymerization of robust polyetheretherketone to regenerate monomer units using sulfur reagents
Yasunori Minami1,2, Nao Matsuyama3, Yasuo Takeichi4
1Interdisciplinary Research Center for Catalytic Chemistry (IRC3), National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8565, Japan. yasu-minami@aist.go.jp.
This study introduces a novel chemical recycling method for super engineering plastics like polyetheretherketone (PEEK). The process effectively depolymerizes PEEK into valuable monomers, enabling further polymerization and sustainable material use.
Area of Science:
- Polymer Chemistry
- Materials Science
- Sustainable Chemistry
Background:
- Super engineering plastics, including polyetheretherketone (PEEK) and polyphenylene sulfide, offer high thermal stability and mechanical strength.
- Their inherent robustness, however, poses significant challenges for depolymerization and chemical recycling into monomers or low-weight molecules.
- Current chemical recycling methods for these advanced polymers remain largely underdeveloped.
Purpose of the Study:
- To develop an effective chemical recycling method for insoluble polyetheretherketone (PEEK).
- To demonstrate the depolymerization of PEEK into useful chemical intermediates.
- To explore the potential for creating new polymers from the recycled products.
Main Methods:
- Depolymerization of polyetheretherketone (PEEK) using sulfur nucleophiles targeting carbon-oxygen bond cleavage.
- Formation of benzophenone dithiolate and hydroquinone as primary depolymerization products.
- Conversion of benzophenone dithiolate with organic halides to yield dithiofunctionalized benzophenones.
Main Results:
- The depolymerization method successfully broke down insoluble PEEK via a solid-liquid reaction, irrespective of its physical form (pellets, films).
- The method proved effective for both neat and fiber-reinforced PEEK (carbon- or glass fiber-enforced).
- Dithiofunctionalized benzophenones were synthesized and subsequently converted to diiodobenzophenone, suitable for polymerization.
Conclusions:
- A novel and efficient chemical recycling pathway for polyetheretherketone (PEEK) has been established.
- This method facilitates the recovery of valuable monomers from robust engineering plastics.
- The derived diiodobenzophenone can be utilized for synthesizing new polymers, promoting a circular economy for high-performance materials.
Related Concept Videos
Free-Radical Chain Reaction and Polymerization of Alkenes
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
Cationic Chain-Growth Polymerization: Mechanism
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...
Hydrolysis
Hydrolysis is a chemical reaction in which the addition of water breaks down a polymer into its simpler monomer units. For example, peptides break into amino acids, carbohydrates into simple sugars, and DNA into nucleotides. Enzymes often facilitate these processes.
Hydrolysis Reverses Dehydration Synthesis
Complex carbohydrates can be broken down by breaking the bonds between individual sugar units. The reaction breaks a glycosidic bond as water is added to the compound. The...
Radical Chain-Growth Polymerization: Overview

