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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...

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Autores principales: Bellotti, Valentina, Parkatzidis, Kostas, Wang, Hyun Suk, De Alwis Watuthanthrige, Nethmi, Orfano, Matteo, Monguzzi, Angelo, Truong, Nghia P., Simonutti, Roberto, Anastasaki, Athina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
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.
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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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