Light-accelerated depolymerization catalyzed by Eosin Y
Retrieving the starting monomers from polymers synthesized by reversible deactivation radical polymerization has recently emerged as an efficient way to increase the recyclability of such materials and potentially enable their industrial implementation. To date, most methods have primarily focused o...
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Veröffentlicht in: | Polymer chemistry 2023-01, Vol.14 (3), p.253-258 |
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creator | Bellotti, Valentina Parkatzidis, Kostas Wang, Hyun Suk De Alwis Watuthanthrige, Nethmi Orfano, Matteo Monguzzi, Angelo Truong, Nghia P Simonutti, Roberto Anastasaki, Athina |
description | Retrieving the starting monomers from polymers synthesized by reversible deactivation radical polymerization has recently emerged as an efficient way to increase the recyclability of such materials and potentially enable their industrial implementation. To date, most methods have primarily focused on utilizing high temperatures (typically from 120 °C to 180 °C) to trigger an efficient depolymerization reaction. In this work, we show that, in the presence of Eosin Y under light irradiation, a much faster depolymerization of polymers made by reversible addition-fragmentation chain-transfer (RAFT) polymerization can be triggered even at a lower temperature (
i.e.
100 °C). For instance, green light, in conjunction with ppm amounts of Eosin Y, resulted in the accelerated depolymerization of poly(methyl methacrylate) from 16% (thermal depolymerization at 100 °C) to 37% within 1 hour, and finally 80% depolymerization after 8 hours, as confirmed by both
1
H-NMR and SEC analyses. The enhanced depolymerization rate was attributed to the activation of a macroCTA by Eosin Y, thus resulting in a faster macroradical generation. Notably, this method was found to be compatible with different wavelengths (
e.g.
blue, red and white light irradiation), solvents, and RAFT agents, thus highlighting the potential of light to significantly improve current depolymerization approaches.
Eosin Y is used as a photocatalyst for the acceleration of the depolymerization of polymethacrylates. |
doi_str_mv | 10.1039/d2py01383e |
format | Article |
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i.e.
100 °C). For instance, green light, in conjunction with ppm amounts of Eosin Y, resulted in the accelerated depolymerization of poly(methyl methacrylate) from 16% (thermal depolymerization at 100 °C) to 37% within 1 hour, and finally 80% depolymerization after 8 hours, as confirmed by both
1
H-NMR and SEC analyses. The enhanced depolymerization rate was attributed to the activation of a macroCTA by Eosin Y, thus resulting in a faster macroradical generation. Notably, this method was found to be compatible with different wavelengths (
e.g.
blue, red and white light irradiation), solvents, and RAFT agents, thus highlighting the potential of light to significantly improve current depolymerization approaches.
Eosin Y is used as a photocatalyst for the acceleration of the depolymerization of polymethacrylates.</description><identifier>ISSN: 1759-9954</identifier><identifier>EISSN: 1759-9962</identifier><identifier>DOI: 10.1039/d2py01383e</identifier><identifier>PMID: 36760607</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Addition polymerization ; Chemistry ; Depolymerization ; High temperature ; Light irradiation ; NMR ; Nuclear magnetic resonance ; Polymer chemistry ; Polymerization ; Polymers ; Polymethyl methacrylate ; Recyclability ; White light</subject><ispartof>Polymer chemistry, 2023-01, Vol.14 (3), p.253-258</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2023</rights><rights>This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-d8f45f7114f9008b7fe09b955c3e1666a5f241519c7f9c0e5f923bc988fd5d383</citedby><cites>FETCH-LOGICAL-c428t-d8f45f7114f9008b7fe09b955c3e1666a5f241519c7f9c0e5f923bc988fd5d383</cites><orcidid>0000-0001-7444-7815 ; 0000-0002-6615-1026 ; 0000-0002-9068-3751 ; 0000-0002-2515-3906 ; 0000-0001-7058-2438 ; 0000-0001-9900-2644</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36760607$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bellotti, Valentina</creatorcontrib><creatorcontrib>Parkatzidis, Kostas</creatorcontrib><creatorcontrib>Wang, Hyun Suk</creatorcontrib><creatorcontrib>De Alwis Watuthanthrige, Nethmi</creatorcontrib><creatorcontrib>Orfano, Matteo</creatorcontrib><creatorcontrib>Monguzzi, Angelo</creatorcontrib><creatorcontrib>Truong, Nghia P</creatorcontrib><creatorcontrib>Simonutti, Roberto</creatorcontrib><creatorcontrib>Anastasaki, Athina</creatorcontrib><title>Light-accelerated depolymerization catalyzed by Eosin Y</title><title>Polymer chemistry</title><addtitle>Polym Chem</addtitle><description>Retrieving the starting monomers from polymers synthesized by reversible deactivation radical polymerization has recently emerged as an efficient way to increase the recyclability of such materials and potentially enable their industrial implementation. To date, most methods have primarily focused on utilizing high temperatures (typically from 120 °C to 180 °C) to trigger an efficient depolymerization reaction. In this work, we show that, in the presence of Eosin Y under light irradiation, a much faster depolymerization of polymers made by reversible addition-fragmentation chain-transfer (RAFT) polymerization can be triggered even at a lower temperature (
i.e.
100 °C). For instance, green light, in conjunction with ppm amounts of Eosin Y, resulted in the accelerated depolymerization of poly(methyl methacrylate) from 16% (thermal depolymerization at 100 °C) to 37% within 1 hour, and finally 80% depolymerization after 8 hours, as confirmed by both
1
H-NMR and SEC analyses. The enhanced depolymerization rate was attributed to the activation of a macroCTA by Eosin Y, thus resulting in a faster macroradical generation. Notably, this method was found to be compatible with different wavelengths (
e.g.
blue, red and white light irradiation), solvents, and RAFT agents, thus highlighting the potential of light to significantly improve current depolymerization approaches.
Eosin Y is used as a photocatalyst for the acceleration of the depolymerization of polymethacrylates.</description><subject>Addition polymerization</subject><subject>Chemistry</subject><subject>Depolymerization</subject><subject>High temperature</subject><subject>Light irradiation</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Polymer chemistry</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Polymethyl methacrylate</subject><subject>Recyclability</subject><subject>White light</subject><issn>1759-9954</issn><issn>1759-9962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkd1LwzAUxYMobsy9-K4UfBGhmjRN0rwIMucHDPRBH_YU0jTZOtpmJp3Q_fVGN-fHfbkXzo_DPRwAjhG8RBDzqyJZdhDhDOs90EeM8JhzmuzvbpL2wND7BQyDUZpgegh6mDIKKWR9wCblbN7GUildaSdbXUSFXtqqq7Ur17ItbRMp2cqqWwcp76Kx9WUTTY_AgZGV18PtHoDXu_HL6CGePN0_jm4msUqTrI2LzKTEMIRSwyHMcmY05DknRGGNKKWSmCRFBHHFDFdQE8MTnCueZaYgRUg1ANcb3-Uqr3WhdNM6WYmlK2vpOmFlKf4qTTkXM_sueJZiGswG4Hxr4OzbSvtW1KUPYSvZaLvyImGMUEQhoQE9-4cu7Mo1IV6gKOEYsowF6mJDKWe9d9rsnkFQfFYibpPn6Vcl4wCf_n5_h34XEICTDeC82qk_neIPm-CQDQ</recordid><startdate>20230117</startdate><enddate>20230117</enddate><creator>Bellotti, Valentina</creator><creator>Parkatzidis, Kostas</creator><creator>Wang, Hyun Suk</creator><creator>De Alwis Watuthanthrige, Nethmi</creator><creator>Orfano, Matteo</creator><creator>Monguzzi, Angelo</creator><creator>Truong, Nghia P</creator><creator>Simonutti, Roberto</creator><creator>Anastasaki, Athina</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7444-7815</orcidid><orcidid>https://orcid.org/0000-0002-6615-1026</orcidid><orcidid>https://orcid.org/0000-0002-9068-3751</orcidid><orcidid>https://orcid.org/0000-0002-2515-3906</orcidid><orcidid>https://orcid.org/0000-0001-7058-2438</orcidid><orcidid>https://orcid.org/0000-0001-9900-2644</orcidid></search><sort><creationdate>20230117</creationdate><title>Light-accelerated depolymerization catalyzed by Eosin Y</title><author>Bellotti, Valentina ; Parkatzidis, Kostas ; Wang, Hyun Suk ; De Alwis Watuthanthrige, Nethmi ; Orfano, Matteo ; Monguzzi, Angelo ; Truong, Nghia P ; Simonutti, Roberto ; Anastasaki, Athina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-d8f45f7114f9008b7fe09b955c3e1666a5f241519c7f9c0e5f923bc988fd5d383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Addition polymerization</topic><topic>Chemistry</topic><topic>Depolymerization</topic><topic>High temperature</topic><topic>Light irradiation</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Polymer chemistry</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Polymethyl methacrylate</topic><topic>Recyclability</topic><topic>White light</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bellotti, Valentina</creatorcontrib><creatorcontrib>Parkatzidis, Kostas</creatorcontrib><creatorcontrib>Wang, Hyun Suk</creatorcontrib><creatorcontrib>De Alwis Watuthanthrige, Nethmi</creatorcontrib><creatorcontrib>Orfano, Matteo</creatorcontrib><creatorcontrib>Monguzzi, Angelo</creatorcontrib><creatorcontrib>Truong, Nghia P</creatorcontrib><creatorcontrib>Simonutti, Roberto</creatorcontrib><creatorcontrib>Anastasaki, Athina</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Polymer chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bellotti, Valentina</au><au>Parkatzidis, Kostas</au><au>Wang, Hyun Suk</au><au>De Alwis Watuthanthrige, Nethmi</au><au>Orfano, Matteo</au><au>Monguzzi, Angelo</au><au>Truong, Nghia P</au><au>Simonutti, Roberto</au><au>Anastasaki, Athina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Light-accelerated depolymerization catalyzed by Eosin Y</atitle><jtitle>Polymer chemistry</jtitle><addtitle>Polym Chem</addtitle><date>2023-01-17</date><risdate>2023</risdate><volume>14</volume><issue>3</issue><spage>253</spage><epage>258</epage><pages>253-258</pages><issn>1759-9954</issn><eissn>1759-9962</eissn><abstract>Retrieving the starting monomers from polymers synthesized by reversible deactivation radical polymerization has recently emerged as an efficient way to increase the recyclability of such materials and potentially enable their industrial implementation. To date, most methods have primarily focused on utilizing high temperatures (typically from 120 °C to 180 °C) to trigger an efficient depolymerization reaction. In this work, we show that, in the presence of Eosin Y under light irradiation, a much faster depolymerization of polymers made by reversible addition-fragmentation chain-transfer (RAFT) polymerization can be triggered even at a lower temperature (
i.e.
100 °C). For instance, green light, in conjunction with ppm amounts of Eosin Y, resulted in the accelerated depolymerization of poly(methyl methacrylate) from 16% (thermal depolymerization at 100 °C) to 37% within 1 hour, and finally 80% depolymerization after 8 hours, as confirmed by both
1
H-NMR and SEC analyses. The enhanced depolymerization rate was attributed to the activation of a macroCTA by Eosin Y, thus resulting in a faster macroradical generation. Notably, this method was found to be compatible with different wavelengths (
e.g.
blue, red and white light irradiation), solvents, and RAFT agents, thus highlighting the potential of light to significantly improve current depolymerization approaches.
Eosin Y is used as a photocatalyst for the acceleration of the depolymerization of polymethacrylates.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>36760607</pmid><doi>10.1039/d2py01383e</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-7444-7815</orcidid><orcidid>https://orcid.org/0000-0002-6615-1026</orcidid><orcidid>https://orcid.org/0000-0002-9068-3751</orcidid><orcidid>https://orcid.org/0000-0002-2515-3906</orcidid><orcidid>https://orcid.org/0000-0001-7058-2438</orcidid><orcidid>https://orcid.org/0000-0001-9900-2644</orcidid><oa>free_for_read</oa></addata></record> |
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source | Royal Society Of Chemistry Journals 2008- |
subjects | Addition polymerization Chemistry Depolymerization High temperature Light irradiation NMR Nuclear magnetic resonance Polymer chemistry Polymerization Polymers Polymethyl methacrylate Recyclability White light |
title | Light-accelerated depolymerization catalyzed by Eosin Y |
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