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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7698803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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