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A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)

In this report we describe repurposing of recycled polyesters as a matrix for lignin-a biorefinery coproduct that is used as a solid fuel and needs to find higher value-to make sustainable high-performance thermoplastic materials. Brittle lignin oligomers, isolated from plant biomass, require a low-...

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Autores principales: Akato, Kokouvi M., Nguyen, Ngoc A., Rajan, Kalavathy, Harper, David P., Naskar, Amit K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072396/
https://www.ncbi.nlm.nih.gov/pubmed/35527949
http://dx.doi.org/10.1039/c9ra07052d
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author Akato, Kokouvi M.
Nguyen, Ngoc A.
Rajan, Kalavathy
Harper, David P.
Naskar, Amit K.
author_facet Akato, Kokouvi M.
Nguyen, Ngoc A.
Rajan, Kalavathy
Harper, David P.
Naskar, Amit K.
author_sort Akato, Kokouvi M.
collection PubMed
description In this report we describe repurposing of recycled polyesters as a matrix for lignin-a biorefinery coproduct that is used as a solid fuel and needs to find higher value-to make sustainable high-performance thermoplastic materials. Brittle lignin oligomers, isolated from plant biomass, require a low-melting host polymer matrix to form a rigid and tough renewable material. We demonstrate controlled lignin dispersion and interfacial interactions in softened recycled polyethylene terephthalate (PET) using a simple solvent-free, melt-blending technique. To avoid lignin degradation and devolatilization during melt processing, it was thermally treated. Tall oil fatty acid was used to enable PET processability at low enough temperature to accommodate lignin without charring. Chemical analysis reveals reduction of aliphatic hydroxyl content from 2 mmol g(−1) to 1.63 mmol g(−1) and an increase of total phenolic hydroxyl moieties from 5.86 to 6.64 mmol g(−1) and cleavage of β-O-4 ether linkages due to thermal treatment. Structural transformation of lignin macromolecules during heat treatment was further confirmed by an increase in molar mass and improved thermal stability. Interfacial interactions between lignin and PET were assessed from mechanical properties and thermal analyses. Thermal treatment not only helps to improve the stability of lignin but also slightly reduces the size of the dispersed lignin domains via favored interfacial interactions with the PET matrix. These methods improve mechanical properties of the material. Further, incorporation of lignin in the plasticized PET matrix increases the ductility in the blended products. The method we discuss here utilizes industrial wastes and co-products, and it does not require solvent or toxic chemicals during the reactive extrusion process that yields complete conversion to products.
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spelling pubmed-90723962022-05-06 A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate) Akato, Kokouvi M. Nguyen, Ngoc A. Rajan, Kalavathy Harper, David P. Naskar, Amit K. RSC Adv Chemistry In this report we describe repurposing of recycled polyesters as a matrix for lignin-a biorefinery coproduct that is used as a solid fuel and needs to find higher value-to make sustainable high-performance thermoplastic materials. Brittle lignin oligomers, isolated from plant biomass, require a low-melting host polymer matrix to form a rigid and tough renewable material. We demonstrate controlled lignin dispersion and interfacial interactions in softened recycled polyethylene terephthalate (PET) using a simple solvent-free, melt-blending technique. To avoid lignin degradation and devolatilization during melt processing, it was thermally treated. Tall oil fatty acid was used to enable PET processability at low enough temperature to accommodate lignin without charring. Chemical analysis reveals reduction of aliphatic hydroxyl content from 2 mmol g(−1) to 1.63 mmol g(−1) and an increase of total phenolic hydroxyl moieties from 5.86 to 6.64 mmol g(−1) and cleavage of β-O-4 ether linkages due to thermal treatment. Structural transformation of lignin macromolecules during heat treatment was further confirmed by an increase in molar mass and improved thermal stability. Interfacial interactions between lignin and PET were assessed from mechanical properties and thermal analyses. Thermal treatment not only helps to improve the stability of lignin but also slightly reduces the size of the dispersed lignin domains via favored interfacial interactions with the PET matrix. These methods improve mechanical properties of the material. Further, incorporation of lignin in the plasticized PET matrix increases the ductility in the blended products. The method we discuss here utilizes industrial wastes and co-products, and it does not require solvent or toxic chemicals during the reactive extrusion process that yields complete conversion to products. The Royal Society of Chemistry 2019-10-01 /pmc/articles/PMC9072396/ /pubmed/35527949 http://dx.doi.org/10.1039/c9ra07052d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Akato, Kokouvi M.
Nguyen, Ngoc A.
Rajan, Kalavathy
Harper, David P.
Naskar, Amit K.
A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)
title A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)
title_full A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)
title_fullStr A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)
title_full_unstemmed A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)
title_short A tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)
title_sort tough and sustainable fiber-forming material from lignin and waste poly(ethylene terephthalate)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072396/
https://www.ncbi.nlm.nih.gov/pubmed/35527949
http://dx.doi.org/10.1039/c9ra07052d
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