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Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings

Novel phosphorylated cardanol molecules based on phosphonate (PO(3)CR) and phosphate (PO(4)CR) functions were synthetized. Those molecules have two main actions which are described in this article: the reduction in volatile organic compounds (VOC) and the development of flame retardant (FR) properti...

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Autores principales: Denis, Maxinne, Le Borgne, Damien, Sonnier, Rodolphe, Caillol, Sylvain, Totee, Cédric, Negrell, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369946/
https://www.ncbi.nlm.nih.gov/pubmed/35956832
http://dx.doi.org/10.3390/molecules27154880
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author Denis, Maxinne
Le Borgne, Damien
Sonnier, Rodolphe
Caillol, Sylvain
Totee, Cédric
Negrell, Claire
author_facet Denis, Maxinne
Le Borgne, Damien
Sonnier, Rodolphe
Caillol, Sylvain
Totee, Cédric
Negrell, Claire
author_sort Denis, Maxinne
collection PubMed
description Novel phosphorylated cardanol molecules based on phosphonate (PO(3)CR) and phosphate (PO(4)CR) functions were synthetized. Those molecules have two main actions which are described in this article: the reduction in volatile organic compounds (VOC) and the development of flame retardant (FR) properties conferred on alkyd resins used as coatings for wood specimen. Phosphorylated cardanol compounds have been successfully grafted by covalent bonds to alkyd resins thanks to an auto-oxidative reaction. The impact of the introduction of PO(3)CR and PO(4)CR on the film properties such as drying time and flexibility has been studied and the thermal and flame retardant properties through differential scanning calorimeter, thermogravimetric analysis and pyrolysis-combustion flow calorimeter. These studies underscored an increase in the thermal stability and FR properties of the alkyd resins. In the cone calorimeter test, the lowest pHRR was obtained with 3 wt% P of phosphate-cardanol and exhibited a value of 170 KW.m(−2), which represented a decrease of almost 46% compared to the PO(x)CR-free alkyd resins. Moreover, a difference in the mode of action between phosphonate and phosphate compounds has been highlighted. The most effective coating which combined excellent FR properties and good coating properties has been obtained with 2 wt% P of phosphate-cardanol. Indeed, the film properties were closed to the PO(x)CR-free alkyd resin and the pHRR decreased by 41% compared to the reference alkyd resin.
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spelling pubmed-93699462022-08-12 Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings Denis, Maxinne Le Borgne, Damien Sonnier, Rodolphe Caillol, Sylvain Totee, Cédric Negrell, Claire Molecules Article Novel phosphorylated cardanol molecules based on phosphonate (PO(3)CR) and phosphate (PO(4)CR) functions were synthetized. Those molecules have two main actions which are described in this article: the reduction in volatile organic compounds (VOC) and the development of flame retardant (FR) properties conferred on alkyd resins used as coatings for wood specimen. Phosphorylated cardanol compounds have been successfully grafted by covalent bonds to alkyd resins thanks to an auto-oxidative reaction. The impact of the introduction of PO(3)CR and PO(4)CR on the film properties such as drying time and flexibility has been studied and the thermal and flame retardant properties through differential scanning calorimeter, thermogravimetric analysis and pyrolysis-combustion flow calorimeter. These studies underscored an increase in the thermal stability and FR properties of the alkyd resins. In the cone calorimeter test, the lowest pHRR was obtained with 3 wt% P of phosphate-cardanol and exhibited a value of 170 KW.m(−2), which represented a decrease of almost 46% compared to the PO(x)CR-free alkyd resins. Moreover, a difference in the mode of action between phosphonate and phosphate compounds has been highlighted. The most effective coating which combined excellent FR properties and good coating properties has been obtained with 2 wt% P of phosphate-cardanol. Indeed, the film properties were closed to the PO(x)CR-free alkyd resin and the pHRR decreased by 41% compared to the reference alkyd resin. MDPI 2022-07-30 /pmc/articles/PMC9369946/ /pubmed/35956832 http://dx.doi.org/10.3390/molecules27154880 Text en © 2022 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
Denis, Maxinne
Le Borgne, Damien
Sonnier, Rodolphe
Caillol, Sylvain
Totee, Cédric
Negrell, Claire
Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings
title Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings
title_full Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings
title_fullStr Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings
title_full_unstemmed Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings
title_short Phosphorus Modified Cardanol: A Greener Route to Reduce VolaTile Organic Compounds and Impart Flame Retardant Properties to Alkyd Resin Coatings
title_sort phosphorus modified cardanol: a greener route to reduce volatile organic compounds and impart flame retardant properties to alkyd resin coatings
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369946/
https://www.ncbi.nlm.nih.gov/pubmed/35956832
http://dx.doi.org/10.3390/molecules27154880
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