Chemical Recycling of Commercial Poly(l-lactic acid) to l-Lactide Using a High-Performance Sn(II)/Alcohol Catalyst System

Thomas M. McGuire, Antoine Buchard, Charlotte Williams

Research output: Contribution to journalArticlepeer-review

26 Citations (SciVal)

Abstract

Poly(l-lactic acid) (PLLA) is a leading commercial polymer produced from biomass, showing useful properties for plastics and fiber applications; after use, it is compostable. One area for improvement is postconsumer waste PLLA chemical recycling to monomer (CRM), i.e., the formation of l-lactide (l-LA) from waste plastic. This process is currently feasible at high reaction temperatures and shows low catalytic activity accompanied, in some cases, by side reactions, including epimerization. Here, a commercial Sn(II) catalyst, applied with nonvolatile commercial alcohol, enables highly efficient CRM of PLLA to yield l-LA in excellent yield and purity (92% yield, >99% l-LA from theoretical max.). The depolymerization is performed using neat polymer films at low temperatures (160 °C) under a nitrogen flow or vacuum. The chemical recycling operates with outstanding activity, achieving turnover frequencies which are up to 3000× higher than previously excellent catalysts and applied at loadings up to 6000× lower than previously leading catalysts. The catalyst system achieves a TOF = 3000 h–1 at 0.01 mol % or 1:10,000 catalyst:PLLA loading. The depolymerization of waste PLLA plastic packaging (coffee cup lids) produces pure l-LA in excellent yield and selectivity. The new catalyst system (Sn + alcohol) can itself be recycled four times in different PLLA “batch degradations” and maintains its high catalytic productivity, activity, and selectivity.
Original languageEnglish
Pages (from-to)19840-19848
Number of pages9
JournalJournal of the American Chemical Society
Volume145
Issue number36
Early online date31 Aug 2023
DOIs
Publication statusPublished - 13 Sept 2023

Bibliographical note

The EPSRC (EP/S018603/1, EP/R027129/1, EP/V003321/1), the Oxford Martin School (Future of Plastics), the Royal Society (UF/160021, URF\R\221027, Fellowship to A.B.), and the UK Catalysis Hub (EP/R027129/1) are acknowledged for research funding.

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