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Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons

In this work, an efficient 3-step process targeting the chemical modification and purification of lignin oligomers from industrial alkaline lignin is described. The oxidative depolymerization process of alkaline lignin with O(2) or Air pressure, without use of metal catalyst, led to the production o...

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Autores principales: Camus, Martin, Condassamy, Olivia, Ham-Pichavant, Frédérique, Michaud, Christelle, Mastroianni, Sergio, Mignani, Gérard, Grau, Etienne, Cramail, Henri, Grelier, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8587034/
https://www.ncbi.nlm.nih.gov/pubmed/34771285
http://dx.doi.org/10.3390/polym13213725
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author Camus, Martin
Condassamy, Olivia
Ham-Pichavant, Frédérique
Michaud, Christelle
Mastroianni, Sergio
Mignani, Gérard
Grau, Etienne
Cramail, Henri
Grelier, Stéphane
author_facet Camus, Martin
Condassamy, Olivia
Ham-Pichavant, Frédérique
Michaud, Christelle
Mastroianni, Sergio
Mignani, Gérard
Grau, Etienne
Cramail, Henri
Grelier, Stéphane
author_sort Camus, Martin
collection PubMed
description In this work, an efficient 3-step process targeting the chemical modification and purification of lignin oligomers from industrial alkaline lignin is described. The oxidative depolymerization process of alkaline lignin with O(2) or Air pressure, without use of metal catalyst, led to the production of two fractions of lignin oligomers named ‘precipitated lignin’ and ‘hydrosoluble lignin’ with 40% and 60% yield, respectively. These fractions were characterized with a wide range of methods including NMR spectroscopy (31P, 2D-HSQC), SEC (in basic media), FTIR. NMR analyses revealed the presence of carboxylic acid functions at a ratio of 1.80 mmol/g and 2.80 mmol/g for the precipitated and hydrosoluble lignin, respectively, values much higher than what is generally found in native lignin (between 0.2 and 0.5 mmol/g). SEC analyses revealed the formation of low molar masses for the precipitated (2200 g/mol) and hydrosoluble fractions (1500 g/mol) in contrast to the alkaline lignin (3900 g/mol). It is worth noting that the hydrosoluble fraction of lignin is soluble in water at any pH. Both processes (oxygen and air) were successfully scaled up and showed similar results in terms of yield and functionalization.
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spelling pubmed-85870342021-11-13 Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons Camus, Martin Condassamy, Olivia Ham-Pichavant, Frédérique Michaud, Christelle Mastroianni, Sergio Mignani, Gérard Grau, Etienne Cramail, Henri Grelier, Stéphane Polymers (Basel) Article In this work, an efficient 3-step process targeting the chemical modification and purification of lignin oligomers from industrial alkaline lignin is described. The oxidative depolymerization process of alkaline lignin with O(2) or Air pressure, without use of metal catalyst, led to the production of two fractions of lignin oligomers named ‘precipitated lignin’ and ‘hydrosoluble lignin’ with 40% and 60% yield, respectively. These fractions were characterized with a wide range of methods including NMR spectroscopy (31P, 2D-HSQC), SEC (in basic media), FTIR. NMR analyses revealed the presence of carboxylic acid functions at a ratio of 1.80 mmol/g and 2.80 mmol/g for the precipitated and hydrosoluble lignin, respectively, values much higher than what is generally found in native lignin (between 0.2 and 0.5 mmol/g). SEC analyses revealed the formation of low molar masses for the precipitated (2200 g/mol) and hydrosoluble fractions (1500 g/mol) in contrast to the alkaline lignin (3900 g/mol). It is worth noting that the hydrosoluble fraction of lignin is soluble in water at any pH. Both processes (oxygen and air) were successfully scaled up and showed similar results in terms of yield and functionalization. MDPI 2021-10-28 /pmc/articles/PMC8587034/ /pubmed/34771285 http://dx.doi.org/10.3390/polym13213725 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Camus, Martin
Condassamy, Olivia
Ham-Pichavant, Frédérique
Michaud, Christelle
Mastroianni, Sergio
Mignani, Gérard
Grau, Etienne
Cramail, Henri
Grelier, Stéphane
Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons
title Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons
title_full Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons
title_fullStr Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons
title_full_unstemmed Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons
title_short Oxidative Depolymerization of Alkaline Lignin from Pinus Pinaster by Oxygen and Air for Value-Added Bio-Sourced Synthons
title_sort oxidative depolymerization of alkaline lignin from pinus pinaster by oxygen and air for value-added bio-sourced synthons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8587034/
https://www.ncbi.nlm.nih.gov/pubmed/34771285
http://dx.doi.org/10.3390/polym13213725
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