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Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis

[Image: see text] The glycolysis reaction of poly(bisphenol A carbonate) (PC) has been explored under 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) catalysis as a potential route to valorize PC wastes by chemical recycling. The amidine base is an active catalyst of PC glycolysis and, under suitable condi...

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Autores principales: Quaranta, Eugenio, Minischetti, Clara Castiglione, Tartaro, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068694/
https://www.ncbi.nlm.nih.gov/pubmed/30087911
http://dx.doi.org/10.1021/acsomega.8b01123
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author Quaranta, Eugenio
Minischetti, Clara Castiglione
Tartaro, Giuseppe
author_facet Quaranta, Eugenio
Minischetti, Clara Castiglione
Tartaro, Giuseppe
author_sort Quaranta, Eugenio
collection PubMed
description [Image: see text] The glycolysis reaction of poly(bisphenol A carbonate) (PC) has been explored under 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) catalysis as a potential route to valorize PC wastes by chemical recycling. The amidine base is an active catalyst of PC glycolysis and, under suitable conditions, promotes effectively and selectively the depolymerization of the polymeric material with 1,2-propanediol or glycerol to give the monomer bisphenol A (BPA) and the relevant cyclic carbonate. The depolymerization process has been investigated under solventless conditions, using diol/triol as the reagent and reaction medium, and also in an auxiliary solvent such as tetrahydrofuran (THF) that is able to dissolve the polymer. The influence of a few experimental parameters (temperature, catalyst load, and reaction time) on the selectivity to cyclic carbonate has been studied. High selectivity to cyclic carbonate has been attained by carrying out the depolymerization reaction in THF and using mild temperature conditions and a stoichiometric amount of polyol. The catalyst can be recovered from the reaction mixture as a BPA/DBU adduct and effectively recycled in a successive run.
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spelling pubmed-60686942018-08-05 Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis Quaranta, Eugenio Minischetti, Clara Castiglione Tartaro, Giuseppe ACS Omega [Image: see text] The glycolysis reaction of poly(bisphenol A carbonate) (PC) has been explored under 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) catalysis as a potential route to valorize PC wastes by chemical recycling. The amidine base is an active catalyst of PC glycolysis and, under suitable conditions, promotes effectively and selectively the depolymerization of the polymeric material with 1,2-propanediol or glycerol to give the monomer bisphenol A (BPA) and the relevant cyclic carbonate. The depolymerization process has been investigated under solventless conditions, using diol/triol as the reagent and reaction medium, and also in an auxiliary solvent such as tetrahydrofuran (THF) that is able to dissolve the polymer. The influence of a few experimental parameters (temperature, catalyst load, and reaction time) on the selectivity to cyclic carbonate has been studied. High selectivity to cyclic carbonate has been attained by carrying out the depolymerization reaction in THF and using mild temperature conditions and a stoichiometric amount of polyol. The catalyst can be recovered from the reaction mixture as a BPA/DBU adduct and effectively recycled in a successive run. American Chemical Society 2018-07-03 /pmc/articles/PMC6068694/ /pubmed/30087911 http://dx.doi.org/10.1021/acsomega.8b01123 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Quaranta, Eugenio
Minischetti, Clara Castiglione
Tartaro, Giuseppe
Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis
title Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis
title_full Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis
title_fullStr Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis
title_full_unstemmed Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis
title_short Chemical Recycling of Poly(bisphenol A carbonate) by Glycolysis under 1,8-Diazabicyclo[5.4.0]undec-7-ene Catalysis
title_sort chemical recycling of poly(bisphenol a carbonate) by glycolysis under 1,8-diazabicyclo[5.4.0]undec-7-ene catalysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068694/
https://www.ncbi.nlm.nih.gov/pubmed/30087911
http://dx.doi.org/10.1021/acsomega.8b01123
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