Reaction of β‐Ketoester and 1,3‐Diol to Access Chemically Recyclable and Mechanically Robust Poly(vinyl alcohol) Thermosets through Incorporation of β‐(1,3‐dioxane)ester

The development of mechanically robust, chemically stable, and yet recyclable polymers represents an essential undertaking in the context of advancing a circular economy for plastics. Here, we introduce a novel cleavable β‐(1,3‐dioxane)ester (DXE) linkage, synthesized through the catalyst‐free react...

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Veröffentlicht in:Angewandte Chemie International Edition 2024-10, Vol.63 (44), p.e202410624-n/a
Hauptverfasser: Ma, Youwei, Zheng, Chihui, Slor, Gadi, Özkan, Melis, Gubelmann, Oliviero Julien, Stellacci, Francesco
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container_issue 44
container_start_page e202410624
container_title Angewandte Chemie International Edition
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creator Ma, Youwei
Zheng, Chihui
Slor, Gadi
Özkan, Melis
Gubelmann, Oliviero Julien
Stellacci, Francesco
description The development of mechanically robust, chemically stable, and yet recyclable polymers represents an essential undertaking in the context of advancing a circular economy for plastics. Here, we introduce a novel cleavable β‐(1,3‐dioxane)ester (DXE) linkage, synthesized through the catalyst‐free reaction of β‐ketoester and 1,3‐diol, to cross‐link poly(vinyl alcohol) (PVA) for the formation of high‐performance thermosets with inherent chemical recyclability. PVA, modified with β‐ketoester groups through the transesterification reaction with excess tert‐butyl acetoacetate, undergoes cross‐linking reactions with the unmodified 1,3‐diols within PVA itself upon thermal treatment. The cross‐linking architecture improves PVA’s mechanical properties, with Young's modulus and toughness that can reach up to 656 MPa and 84 MJ cm−3, i.e. approximately 3‐ and 12‐fold those of linear PVA, respectively. Thermal treatment of the cross‐linked PVA polymers under acid conditions leads to deconstruction of the networks, enabling the excellent recovery (>90 %) of PVA. In the absence of either thermal or acidic treatment, the cross‐linked PVA maintains its dimensional stability. We show that the recovery of PVA is also possible when the treatment is performed in the presence of other plastics commonly found in recycling mixtures. Furthermore, PVA‐based composites comprising carbon fibers and activated charcoal cross‐linked by the DXE linkages are also shown to be recyclable with recovery of the PVA and the fillers. β‐(1,3‐dioxane)ester was designed and used to prepare high‐performance poly(vinyl alcohol) (PVA) via a straightforward modification with β‐ketoesters, followed by the cross‐linking reaction with 1,3‐diol groups. Treatment with HCl solution and heat allows the deconstruction of the cross‐linked PVA, ensuring the selective and quantitative recovery of the initial materials.
doi_str_mv 10.1002/anie.202410624
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source Wiley Online Library Journals Frontfile Complete
subjects 1,3-diol
Activated carbon
Activated charcoal
Carbon fiber reinforced plastics
Charcoal
chemical recycling
Chemical synthesis
Circular economy
Dimensional stability
Diols
Heat treatment
Mechanical properties
Modulus of elasticity
Polymers
Polyvinyl alcohol
Recovery
Recyclability
Robustness
thermoset
Transesterification
β-(1,3-dioxane)ester
β-ketoester
title Reaction of β‐Ketoester and 1,3‐Diol to Access Chemically Recyclable and Mechanically Robust Poly(vinyl alcohol) Thermosets through Incorporation of β‐(1,3‐dioxane)ester
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