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Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations
In this work, we report the synthesis and purification of polyvinyl alcohol-polyaniline (PVA–PANI) copolymers at different aniline concentrations, and their molecular ((1)H-NMR and FTIR), thermal (TGA/DTG/DSC), optical (UV–Vis-NIR), and microstructural (XRD and SEM) properties before and after activ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337460/ https://www.ncbi.nlm.nih.gov/pubmed/30585194 http://dx.doi.org/10.3390/molecules24010063 |
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author | Guerrero, Jorge M. Carrillo, Amanda Mota, María L. Ambrosio, Roberto C. Aguirre, Francisco S. |
author_facet | Guerrero, Jorge M. Carrillo, Amanda Mota, María L. Ambrosio, Roberto C. Aguirre, Francisco S. |
author_sort | Guerrero, Jorge M. |
collection | PubMed |
description | In this work, we report the synthesis and purification of polyvinyl alcohol-polyaniline (PVA–PANI) copolymers at different aniline concentrations, and their molecular ((1)H-NMR and FTIR), thermal (TGA/DTG/DSC), optical (UV–Vis-NIR), and microstructural (XRD and SEM) properties before and after activation with glutaraldehyde (GA) in order to obtain an active membrane. The PVA–PANI copolymers were synthesized by chemical oxidation of aniline using ammonium persulfate (APS) in an acidified (HCl) polyvinyl alcohol matrix. The obtained copolymers were purified by dialysis and the precipitation–redispersion method in order to eliminate undesired products and compare changes due to purification. PVA–PANI products were analyzed as gels, colloidal dispersions, and thin films. (1)H-NMR confirmed the molecular structure of PVA–PANI as the proposed skeletal formula, and FTIR of the obtained purified gels showed the characteristic functional groups of PVA gels with PANI nanoparticles. After exposing the material to a GA solution, the presence of the FTIR absorption bands at 1595 cm(−1), 1650 cm(−1), and 1717 cm(−1) confirmed the activation of the material. FTIR and UV–Vis-NIR characterization showed an increase of the benzenoid section of PANI with GA exposure, which can be interpreted as a reduction of the polymer with the time of activation and concentration of the solution. |
format | Online Article Text |
id | pubmed-6337460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63374602019-01-25 Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations Guerrero, Jorge M. Carrillo, Amanda Mota, María L. Ambrosio, Roberto C. Aguirre, Francisco S. Molecules Article In this work, we report the synthesis and purification of polyvinyl alcohol-polyaniline (PVA–PANI) copolymers at different aniline concentrations, and their molecular ((1)H-NMR and FTIR), thermal (TGA/DTG/DSC), optical (UV–Vis-NIR), and microstructural (XRD and SEM) properties before and after activation with glutaraldehyde (GA) in order to obtain an active membrane. The PVA–PANI copolymers were synthesized by chemical oxidation of aniline using ammonium persulfate (APS) in an acidified (HCl) polyvinyl alcohol matrix. The obtained copolymers were purified by dialysis and the precipitation–redispersion method in order to eliminate undesired products and compare changes due to purification. PVA–PANI products were analyzed as gels, colloidal dispersions, and thin films. (1)H-NMR confirmed the molecular structure of PVA–PANI as the proposed skeletal formula, and FTIR of the obtained purified gels showed the characteristic functional groups of PVA gels with PANI nanoparticles. After exposing the material to a GA solution, the presence of the FTIR absorption bands at 1595 cm(−1), 1650 cm(−1), and 1717 cm(−1) confirmed the activation of the material. FTIR and UV–Vis-NIR characterization showed an increase of the benzenoid section of PANI with GA exposure, which can be interpreted as a reduction of the polymer with the time of activation and concentration of the solution. MDPI 2018-12-25 /pmc/articles/PMC6337460/ /pubmed/30585194 http://dx.doi.org/10.3390/molecules24010063 Text en © 2018 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 Guerrero, Jorge M. Carrillo, Amanda Mota, María L. Ambrosio, Roberto C. Aguirre, Francisco S. Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations |
title | Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations |
title_full | Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations |
title_fullStr | Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations |
title_full_unstemmed | Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations |
title_short | Purification and Glutaraldehyde Activation Study on HCl-Doped PVA–PANI Copolymers with Different Aniline Concentrations |
title_sort | purification and glutaraldehyde activation study on hcl-doped pva–pani copolymers with different aniline concentrations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337460/ https://www.ncbi.nlm.nih.gov/pubmed/30585194 http://dx.doi.org/10.3390/molecules24010063 |
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