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Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy
Polyamide-based thin-film composite nanofiltration membranes are widely used for potable water decontamination, brackish water desalination and wastewater reutilization. However, enhancing the water permeance of the polyamide layer within the thin-film composite nanofiltration membrane still remains...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889836/ https://www.ncbi.nlm.nih.gov/pubmed/31827749 http://dx.doi.org/10.1039/c9sc03088c |
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author | Zhang, Zhe Shi, Xiansong Wang, Rui Xiao, Ankang Wang, Yong |
author_facet | Zhang, Zhe Shi, Xiansong Wang, Rui Xiao, Ankang Wang, Yong |
author_sort | Zhang, Zhe |
collection | PubMed |
description | Polyamide-based thin-film composite nanofiltration membranes are widely used for potable water decontamination, brackish water desalination and wastewater reutilization. However, enhancing the water permeance of the polyamide layer within the thin-film composite nanofiltration membrane still remains a great challenge, because of the relatively large thickness and high transport resistance of the polyamide layer produced by intractable interfacial polymerization. Herein, we reported a two-in-one strategy to prepare ultra-permeable nanofiltration membranes via covalent organic framework (COF) nanofiber scaffold mediated interfacial polymerization. The highly porous and hydrophilic COF nanofiber scaffolds enhanced the controlled release of amine monomers, leading to ultrathin polyamide layers. Also, the relatively smooth COF nanofiber scaffolds can be spontaneously evolved into rugged and uneven architectures during interfacial polymerization, providing rough substrates for enlarging the actual areas of polyamide layers. Therefore, the increased areas of polyamide layers were employed as additional water permeable domains. Arising from the synergetic effect of the ultrathin and increased water permeation domains, the produced membranes exhibit exceptional nanofiltration performance with a water permeance of up to 31.1 L m(–2) h(–1) bar(–1) and a Na(2)SO(4) rejection rate of about 95%, outperforming most other nanofiltration membranes. This highly accessible technique opens a new avenue for the design and engineering of ultra-permeable thin-film composite nanofiltration membranes, highlighting its great potential in providing clean water. |
format | Online Article Text |
id | pubmed-6889836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-68898362019-12-11 Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy Zhang, Zhe Shi, Xiansong Wang, Rui Xiao, Ankang Wang, Yong Chem Sci Chemistry Polyamide-based thin-film composite nanofiltration membranes are widely used for potable water decontamination, brackish water desalination and wastewater reutilization. However, enhancing the water permeance of the polyamide layer within the thin-film composite nanofiltration membrane still remains a great challenge, because of the relatively large thickness and high transport resistance of the polyamide layer produced by intractable interfacial polymerization. Herein, we reported a two-in-one strategy to prepare ultra-permeable nanofiltration membranes via covalent organic framework (COF) nanofiber scaffold mediated interfacial polymerization. The highly porous and hydrophilic COF nanofiber scaffolds enhanced the controlled release of amine monomers, leading to ultrathin polyamide layers. Also, the relatively smooth COF nanofiber scaffolds can be spontaneously evolved into rugged and uneven architectures during interfacial polymerization, providing rough substrates for enlarging the actual areas of polyamide layers. Therefore, the increased areas of polyamide layers were employed as additional water permeable domains. Arising from the synergetic effect of the ultrathin and increased water permeation domains, the produced membranes exhibit exceptional nanofiltration performance with a water permeance of up to 31.1 L m(–2) h(–1) bar(–1) and a Na(2)SO(4) rejection rate of about 95%, outperforming most other nanofiltration membranes. This highly accessible technique opens a new avenue for the design and engineering of ultra-permeable thin-film composite nanofiltration membranes, highlighting its great potential in providing clean water. Royal Society of Chemistry 2019-08-13 /pmc/articles/PMC6889836/ /pubmed/31827749 http://dx.doi.org/10.1039/c9sc03088c Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Zhang, Zhe Shi, Xiansong Wang, Rui Xiao, Ankang Wang, Yong Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy |
title | Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy
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title_full | Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy
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title_fullStr | Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy
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title_full_unstemmed | Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy
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title_short | Ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy
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title_sort | ultra-permeable polyamide membranes harvested by covalent organic framework nanofiber scaffolds: a two-in-one strategy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889836/ https://www.ncbi.nlm.nih.gov/pubmed/31827749 http://dx.doi.org/10.1039/c9sc03088c |
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