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Poly(furfuryl alcohol)-Polycaprolactone Blends

Poly(furfuryl alcohol) (PFA) is a bioresin synthesized from furfuryl alcohol (FA) that is derived from renewable saccharide-rich biomass. In this study, we compounded this bioresin with polycaprolactone (PCL) for the first time, introducing new functional polymer blends. Although PCL is biodegradabl...

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Autores principales: Nanni, Gabriele, Heredia-Guerrero, José A., Paul, Uttam C., Dante, Silvia, Caputo, Gianvito, Canale, Claudio, Athanassiou, Athanassia, Fragouli, Despina, Bayer, Ilker S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630956/
https://www.ncbi.nlm.nih.gov/pubmed/31226802
http://dx.doi.org/10.3390/polym11061069
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author Nanni, Gabriele
Heredia-Guerrero, José A.
Paul, Uttam C.
Dante, Silvia
Caputo, Gianvito
Canale, Claudio
Athanassiou, Athanassia
Fragouli, Despina
Bayer, Ilker S.
author_facet Nanni, Gabriele
Heredia-Guerrero, José A.
Paul, Uttam C.
Dante, Silvia
Caputo, Gianvito
Canale, Claudio
Athanassiou, Athanassia
Fragouli, Despina
Bayer, Ilker S.
author_sort Nanni, Gabriele
collection PubMed
description Poly(furfuryl alcohol) (PFA) is a bioresin synthesized from furfuryl alcohol (FA) that is derived from renewable saccharide-rich biomass. In this study, we compounded this bioresin with polycaprolactone (PCL) for the first time, introducing new functional polymer blends. Although PCL is biodegradable, its production relies on petroleum precursors such as cyclohexanone oils. With the method proposed herein, this dependence on petroleum-derived precursors/monomers is reduced by using PFA without significantly modifying some important properties of the PCL. Polymer blend films were produced by simple solvent casting. The blends were characterized in terms of surface topography by atomic force microscopy (AFM), chemical interactions between PCL and PFA by attenuated total reflection-Fourier transform infrared (ATR-FTIR), crystallinity by XRD, thermal properties by differential scanning calorimetry (DSC), and mechanical properties by tensile tests and biocompatibility by direct and indirect toxicity tests. PFA was found to improve the gas barrier properties of PCL without compromising its mechanical properties, and it demonstrated sustained antioxidant effect with excellent biocompatibility. Our results indicate that these new blends can be potentially used in diverse applications ranging from food packing to biomedical devices.
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spelling pubmed-66309562019-08-19 Poly(furfuryl alcohol)-Polycaprolactone Blends Nanni, Gabriele Heredia-Guerrero, José A. Paul, Uttam C. Dante, Silvia Caputo, Gianvito Canale, Claudio Athanassiou, Athanassia Fragouli, Despina Bayer, Ilker S. Polymers (Basel) Article Poly(furfuryl alcohol) (PFA) is a bioresin synthesized from furfuryl alcohol (FA) that is derived from renewable saccharide-rich biomass. In this study, we compounded this bioresin with polycaprolactone (PCL) for the first time, introducing new functional polymer blends. Although PCL is biodegradable, its production relies on petroleum precursors such as cyclohexanone oils. With the method proposed herein, this dependence on petroleum-derived precursors/monomers is reduced by using PFA without significantly modifying some important properties of the PCL. Polymer blend films were produced by simple solvent casting. The blends were characterized in terms of surface topography by atomic force microscopy (AFM), chemical interactions between PCL and PFA by attenuated total reflection-Fourier transform infrared (ATR-FTIR), crystallinity by XRD, thermal properties by differential scanning calorimetry (DSC), and mechanical properties by tensile tests and biocompatibility by direct and indirect toxicity tests. PFA was found to improve the gas barrier properties of PCL without compromising its mechanical properties, and it demonstrated sustained antioxidant effect with excellent biocompatibility. Our results indicate that these new blends can be potentially used in diverse applications ranging from food packing to biomedical devices. MDPI 2019-06-20 /pmc/articles/PMC6630956/ /pubmed/31226802 http://dx.doi.org/10.3390/polym11061069 Text en © 2019 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
Nanni, Gabriele
Heredia-Guerrero, José A.
Paul, Uttam C.
Dante, Silvia
Caputo, Gianvito
Canale, Claudio
Athanassiou, Athanassia
Fragouli, Despina
Bayer, Ilker S.
Poly(furfuryl alcohol)-Polycaprolactone Blends
title Poly(furfuryl alcohol)-Polycaprolactone Blends
title_full Poly(furfuryl alcohol)-Polycaprolactone Blends
title_fullStr Poly(furfuryl alcohol)-Polycaprolactone Blends
title_full_unstemmed Poly(furfuryl alcohol)-Polycaprolactone Blends
title_short Poly(furfuryl alcohol)-Polycaprolactone Blends
title_sort poly(furfuryl alcohol)-polycaprolactone blends
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630956/
https://www.ncbi.nlm.nih.gov/pubmed/31226802
http://dx.doi.org/10.3390/polym11061069
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