Issue 11, 2024

Chemical recycling of polyolefins via ring-closing metathesis depolymerization

Abstract

The current insufficient recycling of commodity polymer waste has resulted in pressing environmental and human health issues in our modern society. In the quest for next-generation polymer materials, chemists have recently shifted their attention to the design of chemically recyclable polymers that can undergo depolymerization to regenerate monomers under mild conditions. During the past decade, ring-closing metathesis reactions have been demonstrated to be a robust approach for the depolymerization of polyolefins, producing low-strain cyclic alkene products which can be repolymerized back to new batches of polymers. In this review, we aim to highlight the recent advances in chemical recycling of polyolefins enabled by ring-closing metathesis depolymerization (RCMD). A library of depolymerizable polyolefins will be covered based on the ring size of their monomers or depolymerization products, including five-membered, six-membered, eight-membered, and macrocyclic rings. Moreover, current limitations, potential applications, and future opportunities of the RCMD approach will be discussed. It is clear from recent research in this field that RCMD represents a powerful strategy towards closed-loop chemical recycling of novel polyolefin materials.

Graphical abstract: Chemical recycling of polyolefins via ring-closing metathesis depolymerization

Article information

Article type
Highlight
Submitted
15 ноем. 2023
Accepted
04 јан. 2024
First published
04 јан. 2024

Chem. Commun., 2024,60, 1361-1371

Chemical recycling of polyolefins via ring-closing metathesis depolymerization

T. Ibrahim, A. Ritacco, D. Nalley, O. F. Emon, Y. Liang and H. Sun, Chem. Commun., 2024, 60, 1361 DOI: 10.1039/D3CC05612K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements