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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843692/ https://www.ncbi.nlm.nih.gov/pubmed/36760607 http://dx.doi.org/10.1039/d2py01383e |
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author | Bellotti, Valentina Parkatzidis, Kostas Wang, Hyun Suk De Alwis Watuthanthrige, Nethmi Orfano, Matteo Monguzzi, Angelo Truong, Nghia P. Simonutti, Roberto Anastasaki, Athina |
author_facet | Bellotti, Valentina Parkatzidis, Kostas Wang, Hyun Suk De Alwis Watuthanthrige, Nethmi Orfano, Matteo Monguzzi, Angelo Truong, Nghia P. Simonutti, Roberto Anastasaki, Athina |
author_sort | Bellotti, Valentina |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-9843692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-98436922023-02-07 Light-accelerated depolymerization catalyzed by Eosin Y Bellotti, Valentina Parkatzidis, Kostas Wang, Hyun Suk De Alwis Watuthanthrige, Nethmi Orfano, Matteo Monguzzi, Angelo Truong, Nghia P. Simonutti, Roberto Anastasaki, Athina Polym Chem Chemistry 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. The Royal Society of Chemistry 2022-12-20 /pmc/articles/PMC9843692/ /pubmed/36760607 http://dx.doi.org/10.1039/d2py01383e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Bellotti, Valentina Parkatzidis, Kostas Wang, Hyun Suk De Alwis Watuthanthrige, Nethmi Orfano, Matteo Monguzzi, Angelo Truong, Nghia P. Simonutti, Roberto Anastasaki, Athina Light-accelerated depolymerization catalyzed by Eosin Y |
title | Light-accelerated depolymerization catalyzed by Eosin Y |
title_full | Light-accelerated depolymerization catalyzed by Eosin Y |
title_fullStr | Light-accelerated depolymerization catalyzed by Eosin Y |
title_full_unstemmed | Light-accelerated depolymerization catalyzed by Eosin Y |
title_short | Light-accelerated depolymerization catalyzed by Eosin Y |
title_sort | light-accelerated depolymerization catalyzed by eosin y |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843692/ https://www.ncbi.nlm.nih.gov/pubmed/36760607 http://dx.doi.org/10.1039/d2py01383e |
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