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Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin
To develop efficient materials with enhanced adsorption and selectivity for genotoxic 2-aminopyridine in water, based on magnetic chitosan (CTs) and β-cyclodextrin (β-CD), the magnetic molecularly imprinted polymers (MMIPs) of Fe(3)O(4)-CTs@MIP and Fe(3)O(4)-MAH-β-CD@MIP were synthesized by a molecu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615528/ https://www.ncbi.nlm.nih.gov/pubmed/28858259 http://dx.doi.org/10.3390/ijerph14090991 |
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author | Zhang, Wei Zhu, Zhiliang Zhang, Hua Qiu, Yanling |
author_facet | Zhang, Wei Zhu, Zhiliang Zhang, Hua Qiu, Yanling |
author_sort | Zhang, Wei |
collection | PubMed |
description | To develop efficient materials with enhanced adsorption and selectivity for genotoxic 2-aminopyridine in water, based on magnetic chitosan (CTs) and β-cyclodextrin (β-CD), the magnetic molecularly imprinted polymers (MMIPs) of Fe(3)O(4)-CTs@MIP and Fe(3)O(4)-MAH-β-CD@MIP were synthesized by a molecular imprinting technique using 2-aminopyridine as a template. The selective adsorption experiments for 2-aminopyridine were performed by four analogues including pyridine, aniline, 2-amino-5-chloropyridine and phenylenediamine. Results showed the target 2-aminopyridine could be selectively adsorbed and quickly separated by the synthesized MMIPs in the presence of the above structural analogues. The coexisting ions including Na(+), K(+), Mg(2+), Ca(2+), Cl(−) and SO(4)(2−) showed little effect on the adsorption of 2-aminopyridine. The maximum adsorption capacity of 2-aminopyridine on Fe(3)O(4)-CTs@MIP and Fe(3)O(4)-MAH-β-CD@MIP was 39.2 mg·g(−1) and 46.5 mg·g(−1), respectively, which is much higher than values in previous reports. The comparison result with commercial activated carbon showed the obtained MMIPs had higher adsorption ability and selectivity for 2-aminopyridine. In addition, the synthesized MMIPs exhibited excellent performance of regeneration, which was used at least five times with little adsorption capacity loss. Therefore, the synthesized MMIPs are potential effective materials in applications for selective removal and analysis of the genotoxic compound aminopyridine from environmental water. |
format | Online Article Text |
id | pubmed-5615528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56155282017-09-30 Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin Zhang, Wei Zhu, Zhiliang Zhang, Hua Qiu, Yanling Int J Environ Res Public Health Article To develop efficient materials with enhanced adsorption and selectivity for genotoxic 2-aminopyridine in water, based on magnetic chitosan (CTs) and β-cyclodextrin (β-CD), the magnetic molecularly imprinted polymers (MMIPs) of Fe(3)O(4)-CTs@MIP and Fe(3)O(4)-MAH-β-CD@MIP were synthesized by a molecular imprinting technique using 2-aminopyridine as a template. The selective adsorption experiments for 2-aminopyridine were performed by four analogues including pyridine, aniline, 2-amino-5-chloropyridine and phenylenediamine. Results showed the target 2-aminopyridine could be selectively adsorbed and quickly separated by the synthesized MMIPs in the presence of the above structural analogues. The coexisting ions including Na(+), K(+), Mg(2+), Ca(2+), Cl(−) and SO(4)(2−) showed little effect on the adsorption of 2-aminopyridine. The maximum adsorption capacity of 2-aminopyridine on Fe(3)O(4)-CTs@MIP and Fe(3)O(4)-MAH-β-CD@MIP was 39.2 mg·g(−1) and 46.5 mg·g(−1), respectively, which is much higher than values in previous reports. The comparison result with commercial activated carbon showed the obtained MMIPs had higher adsorption ability and selectivity for 2-aminopyridine. In addition, the synthesized MMIPs exhibited excellent performance of regeneration, which was used at least five times with little adsorption capacity loss. Therefore, the synthesized MMIPs are potential effective materials in applications for selective removal and analysis of the genotoxic compound aminopyridine from environmental water. MDPI 2017-08-31 2017-09 /pmc/articles/PMC5615528/ /pubmed/28858259 http://dx.doi.org/10.3390/ijerph14090991 Text en © 2017 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 Zhang, Wei Zhu, Zhiliang Zhang, Hua Qiu, Yanling Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin |
title | Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin |
title_full | Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin |
title_fullStr | Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin |
title_full_unstemmed | Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin |
title_short | Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin |
title_sort | selective removal of the genotoxic compound 2-aminopyridine in water using molecularly imprinted polymers based on magnetic chitosan and β-cyclodextrin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615528/ https://www.ncbi.nlm.nih.gov/pubmed/28858259 http://dx.doi.org/10.3390/ijerph14090991 |
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