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...
Gespeichert in:
Veröffentlicht in: | Angewandte Chemie International Edition 2024-10, Vol.63 (44), p.e202410624-n/a |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | n/a |
---|---|
container_issue | 44 |
container_start_page | e202410624 |
container_title | Angewandte Chemie International Edition |
container_volume | 63 |
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3089878819</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3089878819</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2584-e348be3780981d7d18d47c18e9c1cbd904918f1df3d6e41cba3a307230a545cf3</originalsourceid><addsrcrecordid>eNqFkc1u1DAURiMEoqWwZYkssZlKZPCNncRZjoYCI8qPqrK2HOeGuHLiqZ0A2fEIPAu8Bw_Bk-B2hiLYsLJ1ffzdI31J8hDoEijNnqrB4DKjGQdaZPxWcgh5BikrS3Y73jljaSlyOEjuhXAReSFocTc5YFXEAehh8v0MlR6NG4hryY9vP798fYWjwzCiJ2poCDxhcfbMOEtGR1ZaYwhk3WFvtLJ2JmeoZ21VbfEaf426i0r7N1dPYSTvnJ0XH80wW6Ksdp2zx-S8Q9-7gGMgY-fd9KEjm0E7v3Ve_WWz2Ak0xn1WAx5fi91P7rTKBnywP4-S989Pztcv09O3Lzbr1Wmqs1zwFBkXNbJS0EpAUzYgGl5qEFhp0HVTUV6BaKFpWVMgjyPFFKNlxqjKea5bdpQsdrlb7y6nuFr2Jmi0Npq4KUhGRSVKIaCK6ON_0As3-SHaSQZQFdGigEgtd5T2LgSPrdx60ys_S6Dyqk55Vae8qTN-eLSPneoemxv8d38RqHbAJ2Nx_k-cXL3ZnPwJ_wVoorKA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3119637861</pqid></control><display><type>article</type><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</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Ma, Youwei ; Zheng, Chihui ; Slor, Gadi ; Özkan, Melis ; Gubelmann, Oliviero Julien ; Stellacci, Francesco</creator><creatorcontrib>Ma, Youwei ; Zheng, Chihui ; Slor, Gadi ; Özkan, Melis ; Gubelmann, Oliviero Julien ; Stellacci, Francesco</creatorcontrib><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.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>ISSN: 1521-3773</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202410624</identifier><identifier>PMID: 39106110</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>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</subject><ispartof>Angewandte Chemie International Edition, 2024-10, Vol.63 (44), p.e202410624-n/a</ispartof><rights>2024 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH</rights><rights>2024 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2584-e348be3780981d7d18d47c18e9c1cbd904918f1df3d6e41cba3a307230a545cf3</cites><orcidid>0000-0003-4635-6080</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.202410624$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.202410624$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39106110$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Youwei</creatorcontrib><creatorcontrib>Zheng, Chihui</creatorcontrib><creatorcontrib>Slor, Gadi</creatorcontrib><creatorcontrib>Özkan, Melis</creatorcontrib><creatorcontrib>Gubelmann, Oliviero Julien</creatorcontrib><creatorcontrib>Stellacci, Francesco</creatorcontrib><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</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><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.</description><subject>1,3-diol</subject><subject>Activated carbon</subject><subject>Activated charcoal</subject><subject>Carbon fiber reinforced plastics</subject><subject>Charcoal</subject><subject>chemical recycling</subject><subject>Chemical synthesis</subject><subject>Circular economy</subject><subject>Dimensional stability</subject><subject>Diols</subject><subject>Heat treatment</subject><subject>Mechanical properties</subject><subject>Modulus of elasticity</subject><subject>Polymers</subject><subject>Polyvinyl alcohol</subject><subject>Recovery</subject><subject>Recyclability</subject><subject>Robustness</subject><subject>thermoset</subject><subject>Transesterification</subject><subject>β-(1,3-dioxane)ester</subject><subject>β-ketoester</subject><issn>1433-7851</issn><issn>1521-3773</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqFkc1u1DAURiMEoqWwZYkssZlKZPCNncRZjoYCI8qPqrK2HOeGuHLiqZ0A2fEIPAu8Bw_Bk-B2hiLYsLJ1ffzdI31J8hDoEijNnqrB4DKjGQdaZPxWcgh5BikrS3Y73jljaSlyOEjuhXAReSFocTc5YFXEAehh8v0MlR6NG4hryY9vP798fYWjwzCiJ2poCDxhcfbMOEtGR1ZaYwhk3WFvtLJ2JmeoZ21VbfEaf426i0r7N1dPYSTvnJ0XH80wW6Ksdp2zx-S8Q9-7gGMgY-fd9KEjm0E7v3Ve_WWz2Ak0xn1WAx5fi91P7rTKBnywP4-S989Pztcv09O3Lzbr1Wmqs1zwFBkXNbJS0EpAUzYgGl5qEFhp0HVTUV6BaKFpWVMgjyPFFKNlxqjKea5bdpQsdrlb7y6nuFr2Jmi0Npq4KUhGRSVKIaCK6ON_0As3-SHaSQZQFdGigEgtd5T2LgSPrdx60ys_S6Dyqk55Vae8qTN-eLSPneoemxv8d38RqHbAJ2Nx_k-cXL3ZnPwJ_wVoorKA</recordid><startdate>20241024</startdate><enddate>20241024</enddate><creator>Ma, Youwei</creator><creator>Zheng, Chihui</creator><creator>Slor, Gadi</creator><creator>Özkan, Melis</creator><creator>Gubelmann, Oliviero Julien</creator><creator>Stellacci, Francesco</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4635-6080</orcidid></search><sort><creationdate>20241024</creationdate><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</title><author>Ma, Youwei ; Zheng, Chihui ; Slor, Gadi ; Özkan, Melis ; Gubelmann, Oliviero Julien ; Stellacci, Francesco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2584-e348be3780981d7d18d47c18e9c1cbd904918f1df3d6e41cba3a307230a545cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>1,3-diol</topic><topic>Activated carbon</topic><topic>Activated charcoal</topic><topic>Carbon fiber reinforced plastics</topic><topic>Charcoal</topic><topic>chemical recycling</topic><topic>Chemical synthesis</topic><topic>Circular economy</topic><topic>Dimensional stability</topic><topic>Diols</topic><topic>Heat treatment</topic><topic>Mechanical properties</topic><topic>Modulus of elasticity</topic><topic>Polymers</topic><topic>Polyvinyl alcohol</topic><topic>Recovery</topic><topic>Recyclability</topic><topic>Robustness</topic><topic>thermoset</topic><topic>Transesterification</topic><topic>β-(1,3-dioxane)ester</topic><topic>β-ketoester</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Youwei</creatorcontrib><creatorcontrib>Zheng, Chihui</creatorcontrib><creatorcontrib>Slor, Gadi</creatorcontrib><creatorcontrib>Özkan, Melis</creatorcontrib><creatorcontrib>Gubelmann, Oliviero Julien</creatorcontrib><creatorcontrib>Stellacci, Francesco</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Youwei</au><au>Zheng, Chihui</au><au>Slor, Gadi</au><au>Özkan, Melis</au><au>Gubelmann, Oliviero Julien</au><au>Stellacci, Francesco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2024-10-24</date><risdate>2024</risdate><volume>63</volume><issue>44</issue><spage>e202410624</spage><epage>n/a</epage><pages>e202410624-n/a</pages><issn>1433-7851</issn><issn>1521-3773</issn><eissn>1521-3773</eissn><abstract>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.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>39106110</pmid><doi>10.1002/anie.202410624</doi><tpages>11</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0003-4635-6080</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1433-7851 |
ispartof | Angewandte Chemie International Edition, 2024-10, Vol.63 (44), p.e202410624-n/a |
issn | 1433-7851 1521-3773 1521-3773 |
language | eng |
recordid | cdi_proquest_miscellaneous_3089878819 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T00%3A05%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Reaction%20of%20%CE%B2%E2%80%90Ketoester%20and%201,3%E2%80%90Diol%20to%20Access%20Chemically%20Recyclable%20and%20Mechanically%20Robust%20Poly(vinyl%20alcohol)%20Thermosets%20through%20Incorporation%20of%20%CE%B2%E2%80%90(1,3%E2%80%90dioxane)ester&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Ma,%20Youwei&rft.date=2024-10-24&rft.volume=63&rft.issue=44&rft.spage=e202410624&rft.epage=n/a&rft.pages=e202410624-n/a&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.202410624&rft_dat=%3Cproquest_cross%3E3089878819%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3119637861&rft_id=info:pmid/39106110&rfr_iscdi=true |