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Ambient Temperature Self-Blowing Tannin-Humins Biofoams

Ambient temperature self-blowing tannin–furanic foams have been prepared by substituting a great part—even a majority—of furfuryl alcohol with humins, a polyfuranic material derived from the acid treatment at high temperature of fructose. Closed-cell foams were prepared at room temperature and curin...

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Autores principales: Chen, Xinyi, Guigo, Nathanael, Pizzi, Antonio, Sbirrazzuoli, Nicolas, Li, Bin, Fredon, Emmanuel, Gerardin, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698803/
https://www.ncbi.nlm.nih.gov/pubmed/33213107
http://dx.doi.org/10.3390/polym12112732
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author Chen, Xinyi
Guigo, Nathanael
Pizzi, Antonio
Sbirrazzuoli, Nicolas
Li, Bin
Fredon, Emmanuel
Gerardin, Christine
author_facet Chen, Xinyi
Guigo, Nathanael
Pizzi, Antonio
Sbirrazzuoli, Nicolas
Li, Bin
Fredon, Emmanuel
Gerardin, Christine
author_sort Chen, Xinyi
collection PubMed
description Ambient temperature self-blowing tannin–furanic foams have been prepared by substituting a great part—even a majority—of furfuryl alcohol with humins, a polyfuranic material derived from the acid treatment at high temperature of fructose. Closed-cell foams were prepared at room temperature and curing, while interconnected-cell foams were prepared at 80 °C and curing, this being due to the more vigorous evaporation of the solvent. These foams appear to present similar characteristics as other tannin–furanic foams based only on furfuryl alcohol. A series of tannin–humins–furfuryl alcohol oligomer structures have been defined indicating that all three reagents co-react. Humins appeared to react well with condensed tannins, even higher molecular weight humins species, and even at ambient temperature, but they react slower than furfuryl alcohol. This is due to their high average molecular weight and high viscosity, causing their reaction with other species to be diffusion controlled. Thus, small increases in solvent led to foams with less cracks and open structures. It showed that furfuryl alcohol appears to also have a role as a humins solvent, and not just as a co-reagent and self-polymerization heat generator for foam expansion and hardening. Stress-strain for the different foams showed a higher compressive strength for both the foam with the lowest and the highest proportion of humins, thus in the dominant proportions of either furfuryl alcohol or the humins. Thus, due to their slower reactivity as their proportion increases to a certain critical level, more of them do proportionally participate within the expansion/curing time of the foam to the reaction.
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spelling pubmed-76988032020-11-29 Ambient Temperature Self-Blowing Tannin-Humins Biofoams Chen, Xinyi Guigo, Nathanael Pizzi, Antonio Sbirrazzuoli, Nicolas Li, Bin Fredon, Emmanuel Gerardin, Christine Polymers (Basel) Article Ambient temperature self-blowing tannin–furanic foams have been prepared by substituting a great part—even a majority—of furfuryl alcohol with humins, a polyfuranic material derived from the acid treatment at high temperature of fructose. Closed-cell foams were prepared at room temperature and curing, while interconnected-cell foams were prepared at 80 °C and curing, this being due to the more vigorous evaporation of the solvent. These foams appear to present similar characteristics as other tannin–furanic foams based only on furfuryl alcohol. A series of tannin–humins–furfuryl alcohol oligomer structures have been defined indicating that all three reagents co-react. Humins appeared to react well with condensed tannins, even higher molecular weight humins species, and even at ambient temperature, but they react slower than furfuryl alcohol. This is due to their high average molecular weight and high viscosity, causing their reaction with other species to be diffusion controlled. Thus, small increases in solvent led to foams with less cracks and open structures. It showed that furfuryl alcohol appears to also have a role as a humins solvent, and not just as a co-reagent and self-polymerization heat generator for foam expansion and hardening. Stress-strain for the different foams showed a higher compressive strength for both the foam with the lowest and the highest proportion of humins, thus in the dominant proportions of either furfuryl alcohol or the humins. Thus, due to their slower reactivity as their proportion increases to a certain critical level, more of them do proportionally participate within the expansion/curing time of the foam to the reaction. MDPI 2020-11-17 /pmc/articles/PMC7698803/ /pubmed/33213107 http://dx.doi.org/10.3390/polym12112732 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Xinyi
Guigo, Nathanael
Pizzi, Antonio
Sbirrazzuoli, Nicolas
Li, Bin
Fredon, Emmanuel
Gerardin, Christine
Ambient Temperature Self-Blowing Tannin-Humins Biofoams
title Ambient Temperature Self-Blowing Tannin-Humins Biofoams
title_full Ambient Temperature Self-Blowing Tannin-Humins Biofoams
title_fullStr Ambient Temperature Self-Blowing Tannin-Humins Biofoams
title_full_unstemmed Ambient Temperature Self-Blowing Tannin-Humins Biofoams
title_short Ambient Temperature Self-Blowing Tannin-Humins Biofoams
title_sort ambient temperature self-blowing tannin-humins biofoams
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698803/
https://www.ncbi.nlm.nih.gov/pubmed/33213107
http://dx.doi.org/10.3390/polym12112732
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