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A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection
An environment-friendly fluorescent nano-hybrid hydrogel has been synthesized successfully, from cellulose nanocrystal (CNC), acrylic acid (AA) and phosphorescent Eu(2+)/Dy(3+) doped SrAl(2)O(4) via free radical polymerization. The hydrogel network matrix fixed Eu(2+)/Dy(3+) doped SrAl(2)O(4) nanopa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491507/ https://www.ncbi.nlm.nih.gov/pubmed/28663542 http://dx.doi.org/10.1038/s41598-017-04542-7 |
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author | Wu, Yiqiang Wang, Lijun Qing, Yan Yan, Ning Tian, Cuihua Huang, Yuanxin |
author_facet | Wu, Yiqiang Wang, Lijun Qing, Yan Yan, Ning Tian, Cuihua Huang, Yuanxin |
author_sort | Wu, Yiqiang |
collection | PubMed |
description | An environment-friendly fluorescent nano-hybrid hydrogel has been synthesized successfully, from cellulose nanocrystal (CNC), acrylic acid (AA) and phosphorescent Eu(2+)/Dy(3+) doped SrAl(2)O(4) via free radical polymerization. The hydrogel network matrix fixed Eu(2+)/Dy(3+) doped SrAl(2)O(4) nanoparticles by polymer chains with coordinate bonds that prevented particles from aggregating and quenching in water. The fluorescent nano-hybrid hydrogel exhibited extremely high water absorption of which the swelling ratio in distilled water and NaCl salt solution were respectively of 323.35 g/g and 32.65 g/g. Furthermore, the hydrogel displayed excellent water retention property that can keep half of the moisture even exposed to 80 °C for 210 min. Besides, the hydrogel had bright green fluorescence under the sunlight or ultraviolet excitation, and the fluorescence intensity was up to 125477 after swelling 50 times in water. The time-resolved photoluminescence (TRPL) afterglow decay examination showed that the fluorescent emission persisted for 4 h after hydrogels excited at 368 nm wavelength UV-light for 10 min. The fluorescence intensity behaved significant linear relationship with the swelling ratio. As a result, these hydrogels were considered as promising candidates for the preparation of stable and sensitive sensor materials in green water detection. |
format | Online Article Text |
id | pubmed-5491507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54915072017-07-05 A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection Wu, Yiqiang Wang, Lijun Qing, Yan Yan, Ning Tian, Cuihua Huang, Yuanxin Sci Rep Article An environment-friendly fluorescent nano-hybrid hydrogel has been synthesized successfully, from cellulose nanocrystal (CNC), acrylic acid (AA) and phosphorescent Eu(2+)/Dy(3+) doped SrAl(2)O(4) via free radical polymerization. The hydrogel network matrix fixed Eu(2+)/Dy(3+) doped SrAl(2)O(4) nanoparticles by polymer chains with coordinate bonds that prevented particles from aggregating and quenching in water. The fluorescent nano-hybrid hydrogel exhibited extremely high water absorption of which the swelling ratio in distilled water and NaCl salt solution were respectively of 323.35 g/g and 32.65 g/g. Furthermore, the hydrogel displayed excellent water retention property that can keep half of the moisture even exposed to 80 °C for 210 min. Besides, the hydrogel had bright green fluorescence under the sunlight or ultraviolet excitation, and the fluorescence intensity was up to 125477 after swelling 50 times in water. The time-resolved photoluminescence (TRPL) afterglow decay examination showed that the fluorescent emission persisted for 4 h after hydrogels excited at 368 nm wavelength UV-light for 10 min. The fluorescence intensity behaved significant linear relationship with the swelling ratio. As a result, these hydrogels were considered as promising candidates for the preparation of stable and sensitive sensor materials in green water detection. Nature Publishing Group UK 2017-06-29 /pmc/articles/PMC5491507/ /pubmed/28663542 http://dx.doi.org/10.1038/s41598-017-04542-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wu, Yiqiang Wang, Lijun Qing, Yan Yan, Ning Tian, Cuihua Huang, Yuanxin A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection |
title | A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection |
title_full | A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection |
title_fullStr | A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection |
title_full_unstemmed | A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection |
title_short | A green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection |
title_sort | green route to prepare fluorescent and absorbent nano-hybrid hydrogel for water detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491507/ https://www.ncbi.nlm.nih.gov/pubmed/28663542 http://dx.doi.org/10.1038/s41598-017-04542-7 |
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