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用于增强水过滤的双面共价有机框架膜的可调润湿性

Tunable Wettability of a Dual-Faced Covalent Organic Framework Membrane for Enhanced Water Filtration.

作者信息

Benyettou Farah, Jrad Asmaa, Matouk Zineb, Prakasam Thirumurugan, Hamoud Houeida Issa, Clet Guillaume, Varghese Sabu, Das Gobinda, Khair Mostafa, Sharma Sudhir Kumar, Garai Bikash, AbdulHalim Rasha G, Alkaabi Maryam, Aburabie Jamaliah, Thomas Sneha, Weston James, Pasricha Renu, Jagannathan Ramesh, Gándara Felipe, El-Roz Mohamad, Trabolsi Ali

机构信息

Chemistry Program, New York University Abu Dhabi (NYUAD), Abu Dhabi 129188, United Arab Emirates.

NYUAD Water Research Center, New York University Abu Dhabi (NYUAD), 129188 Abu Dhabi , United Arab Emirates.

出版信息

J Am Chem Soc. 2024 Aug 21;146(33):23537-23554. doi: 10.1021/jacs.4c07559. Epub 2024 Aug 7.

DOI:10.1021/jacs.4c07559
PMID:39110940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11345768/
Abstract

Membrane technology plays a central role in advancing separation processes, particularly in water treatment. Covalent organic frameworks (COFs) have transformative potential in this field due to their adjustable structures and robustness. However, conventional COF membrane synthesis methods are often associated with challenges, such as time-consuming processes and limited control over surface properties. Our study demonstrates a rapid, microwave-assisted method to synthesize self-standing COF membranes within minutes. This approach allows control over the wettability of the surface and achieves superhydrophilic and near-hydrophobic properties. A thorough characterization of the membrane allows a detailed analysis of the membrane properties and the difference in wettability between its two faces. Microwave activation accelerates the self-assembly of the COF nanosheets, whereby the thickness of the membrane can be controlled by adjusting the time of the reaction. The superhydrophilic vapor side of the membrane results from -NH reactions with acetic acid, while the nearly hydrophobic dioxane side has terminal aldehyde groups. Leveraging the superhydrophilic face, water filtration at high water flux, complete oil removal, increased rejection with anionic dye size, and resistance to organic fouling were achieved. The TTA-DFP-COF membrane opens new avenues for research to address the urgent need for water purification, distinguished by its synthesis speed, simplicity, and superior separation capabilities.

摘要

膜技术在推进分离过程中发挥着核心作用,尤其是在水处理方面。共价有机框架(COF)由于其可调节的结构和稳定性,在该领域具有变革潜力。然而,传统的COF膜合成方法往往伴随着诸多挑战,如耗时的过程以及对表面性质的控制有限。我们的研究展示了一种快速的、微波辅助的方法,可在数分钟内合成自立式COF膜。这种方法能够控制表面的润湿性,实现超亲水和近疏水性能。对该膜的全面表征有助于详细分析膜的性质及其两面润湿性的差异。微波活化加速了COF纳米片的自组装,由此可通过调整反应时间来控制膜的厚度。膜的超亲水蒸汽侧是由 -NH 与乙酸反应形成的,而近疏水的二氧六环侧具有末端醛基。利用超亲水面,实现了高水通量下的水过滤、完全除油、对阴离子染料尺寸的截留率增加以及抗有机污染性能。TTA-DFP-COF膜以其合成速度、简便性和卓越的分离能力,为满足水净化的迫切需求开辟了新的研究途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a97/11345768/8be832ad26e7/ja4c07559_0008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a97/11345768/dc4719974136/ja4c07559_0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a97/11345768/8be832ad26e7/ja4c07559_0008.jpg

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