Related Experiment Video
Updated: Sep 11, 2025

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
Published on: November 30, 2020
A general esterolysis strategy for upcycling waste polyesters into high-value esters
Minghao Zhang1,2, Yunkai Yu1,2, Buxing Han3
1State Key Laboratory of Soil Pollution Control and Safety, Zhejiang University, Hangzhou, China.
Abstract:
The upcycling of waste polyesters into high-value chemicals offers a sustainable and economically viable solution to the global plastic waste crisis. Herein, we report a general esterolysis strategy for the efficient depolymerization of polyesters to produce high-value ester products, utilizing a broad range of esters, including carboxylates, carbonates, and C/Si/Ti/P-based esters. Using the 1-ethyl-3-methylimidazolium acetate as a highly effective catalyst, polyethylene terephthalate is selectively converted into dimethyl terephthalate and ethylene carbonate with remarkable yields of 99% and 90%, respectively. Mechanistic studies reveal that methanol, generated in situ via the 1-ethyl-3-methylimidazolium acetate-catalyzed hydrolysis of dimethyl carbonate, drives the cleavage of C-O ester bonds in polyethylene terephthalate. This strategy demonstrates broad applicability, achieving high conversion efficiencies across various mixed and colored commercial waste polyesters. The energy efficiency and versatility of this approach establish a transformative route to diverse high-value esters, advancing the development of circular plastic economies and sustainable chemistry.
Related Concept Videos
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...
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
β-Dicarbonyl Compounds via Crossed Claisen Condensations

