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Better Material Properties and Faster Catalyzed Chemical Recycling for Poly( L ‐Lactide) Using a Simple Commercial Glycerol Ethoxylate Additive

Abstract:
Poly(L‐lactide) (PLLA) is the largest volume commercial bio‐derived plastic, but its brittleness and end‐of‐life recycling remain challenges. Here, glycerol ethoxylate (GEO), a branched ethylene glycol derivative, both toughens commercial PLLA and accelerates its catalyzed chemical recycling to L‐lactide. A series of GEO–PLLA blends, containing 2–20 wt.% GEO, show significantly improved ductility and toughening compared to pure PLLA. The lead 10 wt.% GEO–PLLA sample achieves 9x higher elongation at break (191% ± 4%) and 6x higher tensile toughness (57.9 ± 1.9 MJ m−3), while retaining desirable tensile strength (36.3 ± 1.5 MPa), thermal properties (Tg = 39°C and Tm = 149°C) and crystallinity (25%). The GEO–PLLA samples are efficiently chemically recycled to L‐lactide, showing both high recycling activity (TOF = 2240 ± 73 h−1) and quantitative selectivity for L‐lactide (> 99%). The recycling is performed neat, at 180°C, using low loadings of commercial Sn(II)Oct2 catalyst. The 10 wt.% GEO–PLLA sample shows significantly faster chemical recycling than PLLA, with kobs = 22.9 ± 0.8 h−1 versus kobs = 1.8 ± 0.2 h−1 for PLLA. This recycling process is successful even with contamination from other commercial plastics, demonstrating its applicability to future postconsumer waste streams.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/chem.202600008

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Institution:
University of Oxford
Role:
Author
ORCID:
0009-0006-9147-8596
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-2719-1228
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-6573-0926
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-8099-9517
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-0734-1575



Publisher:
Wiley
Journal:
Chemistry - A European Journal More from this journal
Pages:
e00008
Article number:
e00008
Publication date:
2026-03-09
Acceptance date:
2026-02-18
DOI:
EISSN:
1521-3765
ISSN:
0947-6539


Language:
English
Keywords:
Pubs id:
2387409
Local pid:
pubs:2387409
Source identifiers:
3837247
Deposit date:
2026-03-10
ARK identifier:
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