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Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates)

Due to its excellent properties, poly(ethylene terephthalate) (PET) is one of the most produced and consumed polymers. Among plastics, it represents the main contributor to environmental pollution. Following the circular economy model, the chemical upcycling of PET reduces the amount of waste genera...

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Autores principales: Pastore, Genny, Giacomantonio, Roberto, Lupidi, Gabriele, Stella, Francesca, Risoluti, Roberta, Papa, Elena, Ballini, Roberto, Sarasini, Fabrizio, Tirillò, Jacopo, Marcantoni, Enrico, Gabrielli, Serena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374216/
https://www.ncbi.nlm.nih.gov/pubmed/37521014
http://dx.doi.org/10.3389/fchem.2023.1234763
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author Pastore, Genny
Giacomantonio, Roberto
Lupidi, Gabriele
Stella, Francesca
Risoluti, Roberta
Papa, Elena
Ballini, Roberto
Sarasini, Fabrizio
Tirillò, Jacopo
Marcantoni, Enrico
Gabrielli, Serena
author_facet Pastore, Genny
Giacomantonio, Roberto
Lupidi, Gabriele
Stella, Francesca
Risoluti, Roberta
Papa, Elena
Ballini, Roberto
Sarasini, Fabrizio
Tirillò, Jacopo
Marcantoni, Enrico
Gabrielli, Serena
author_sort Pastore, Genny
collection PubMed
description Due to its excellent properties, poly(ethylene terephthalate) (PET) is one of the most produced and consumed polymers. Among plastics, it represents the main contributor to environmental pollution. Following the circular economy model, the chemical upcycling of PET reduces the amount of waste generated and transforms it into high-value products. The depolymerization of poly(ethylene terephthalate) into oligomers or monomers leads to forming a library of reactive molecules involved in different polymerization processes to obtain compounds with improved properties. Herein, several β-hydroxy amines were synthesized and used for the chemical recycling of water bottle waste by an environmental benefit aminolysis process to get very useful new terephthalamide diol monomers. The recycled diol monomers were subsequently exploited to synthesize poly(urethane acrylates) (PUAs) UV-curable coatings, and their chemical, thermal and mechanical characterizations were performed. The results show the great potential of the developed synthesis protocols to obtain PUAs with final properties that can be modulated to meet the requirements of different applications.
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spelling pubmed-103742162023-07-28 Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates) Pastore, Genny Giacomantonio, Roberto Lupidi, Gabriele Stella, Francesca Risoluti, Roberta Papa, Elena Ballini, Roberto Sarasini, Fabrizio Tirillò, Jacopo Marcantoni, Enrico Gabrielli, Serena Front Chem Chemistry Due to its excellent properties, poly(ethylene terephthalate) (PET) is one of the most produced and consumed polymers. Among plastics, it represents the main contributor to environmental pollution. Following the circular economy model, the chemical upcycling of PET reduces the amount of waste generated and transforms it into high-value products. The depolymerization of poly(ethylene terephthalate) into oligomers or monomers leads to forming a library of reactive molecules involved in different polymerization processes to obtain compounds with improved properties. Herein, several β-hydroxy amines were synthesized and used for the chemical recycling of water bottle waste by an environmental benefit aminolysis process to get very useful new terephthalamide diol monomers. The recycled diol monomers were subsequently exploited to synthesize poly(urethane acrylates) (PUAs) UV-curable coatings, and their chemical, thermal and mechanical characterizations were performed. The results show the great potential of the developed synthesis protocols to obtain PUAs with final properties that can be modulated to meet the requirements of different applications. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10374216/ /pubmed/37521014 http://dx.doi.org/10.3389/fchem.2023.1234763 Text en Copyright © 2023 Pastore, Giacomantonio, Lupidi, Stella, Risoluti, Papa, Ballini, Sarasini, Tirillò, Marcantoni and Gabrielli. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Pastore, Genny
Giacomantonio, Roberto
Lupidi, Gabriele
Stella, Francesca
Risoluti, Roberta
Papa, Elena
Ballini, Roberto
Sarasini, Fabrizio
Tirillò, Jacopo
Marcantoni, Enrico
Gabrielli, Serena
Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates)
title Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates)
title_full Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates)
title_fullStr Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates)
title_full_unstemmed Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates)
title_short Novel terephthalamide diol monomers synthesis from PET waste to Poly(Urethane acrylates)
title_sort novel terephthalamide diol monomers synthesis from pet waste to poly(urethane acrylates)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374216/
https://www.ncbi.nlm.nih.gov/pubmed/37521014
http://dx.doi.org/10.3389/fchem.2023.1234763
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