Issue 18, 2025

Catalytic alkaline hydrolysis of PET and BPA-PC waste in minutes at atmospheric pressure without microwaves or organic solvents

Abstract

Rapid hydrolysis of poly(ethylene terephthalate) (PET) waste usually requires organic cosolvents, high pressures or microwave irradiation, which can increase the environmental impact/expense/operational complexity of an emerging enabling technology for more sustainable plastic recycling. Using a combination of solute-derived boiling point elevation and phase transfer catalysis, operationally facile, rapid alkaline hydrolysis of PET and poly(bisphenol A carbonate) (BPA-PC) waste – from beverage bottles/textiles and compact discs respectively – is achievable in minutes (≤5 min for PET and 20 min for BPA-PC) at atmospheric pressure without the need for either microwaves or organic cosolvents. Dimethyldialkylammonium halides were found to be optimal catalysts at low loadings. The rapid, one-pot catalytic hydrolysis of a waste stream of both plastics followed by ready isolation of the terephthalic acid and bis-phenol A monomer units in excellent yields (without decomposition) is possible by selective protonolysis.

Graphical abstract: Catalytic alkaline hydrolysis of PET and BPA-PC waste in minutes at atmospheric pressure without microwaves or organic solvents

Supplementary files

Article information

Article type
Communication
Submitted
06 Mar 2025
Accepted
31 Mar 2025
First published
11 Apr 2025
This article is Open Access
Creative Commons BY license

Green Chem., 2025,27, 4986-4994

Catalytic alkaline hydrolysis of PET and BPA-PC waste in minutes at atmospheric pressure without microwaves or organic solvents

A. Jain and S. J. Connon, Green Chem., 2025, 27, 4986 DOI: 10.1039/D5GC01183C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements