Nanofiltration Membranes Formed through Interfacial Polymerization Involving Cycloalkane Amine Monomer and Trimesoyl Chloride Showing Some Tolerance to Chlorine during Dye Desalination

Bibliographic Details
Title: Nanofiltration Membranes Formed through Interfacial Polymerization Involving Cycloalkane Amine Monomer and Trimesoyl Chloride Showing Some Tolerance to Chlorine during Dye Desalination
Authors: Micah Belle Marie Yap Ang, Yi-Ling Wu, Min-Yi Chu, Ping-Han Wu, Yu-Hsuan Chiao, Jeremiah C. Millare, Shu-Hsien Huang, Hui-An Tsai, Kueir-Rarn Lee
Source: Membranes, Vol 12, Iss 3, p 333 (2022)
Publisher Information: MDPI AG, 2022.
Publication Year: 2022
Collection: LCC:Chemical technology
LCC:Chemical engineering
Subject Terms: cycloalkane amine, dye desalination, chlorine-resistant membrane, nanofiltration, polyamide membrane, Chemical technology, TP1-1185, Chemical engineering, TP155-156
More Details: Wastewater effluents containing high concentrations of dyes are highly toxic to the environment and aquatic organisms. Recycle and reuse of both water and dye in textile industries can save energy and costs. Thus, new materials are being explored to fabricate highly efficient nanofiltration membranes for fulfilling industrial needs. In this work, three diamines, 1,4-cyclohexanediamine (CHD), ethylenediamine (EDA), and p-phenylenediamine (PPD), are reacted with TMC separately to fabricate a thin film composite polyamide membrane for dye desalination. Their chemical structures are different, with the difference located in the middle of two terminal amines. The surface morphology, roughness, and thickness of the polyamide layer are dependent on the reactivity of the diamines with TMC. EDA has a short linear alkane chain, which can easily react with TMC, forming a very dense selective layer. CHD has a cyclohexane ring, making it more sterically hindered than EDA. As such, CHD’s reaction with TMC is slower than EDA’s, leading to a thinner polyamide layer. PPD has a benzene ring, which should make it the most sterically hindered structure; however, its benzene ring has a pi-pi interaction with TMC that can facilitate a faster reaction between PPD and TMC, leading to a thicker polyamide layer. Among the TFC membranes, TFCCHD exhibited the highest separation efficiency (pure water flux = 192.13 ± 7.11 L∙m−2∙h−1, dye rejection = 99.92 ± 0.10%, and NaCl rejection = 15.46 ± 1.68% at 6 bar and 1000 ppm salt or 50 ppm of dye solution). After exposure at 12,000 ppm∙h of active chlorine, the flux of TFCCHD was enhanced with maintained high dye rejection. Therefore, the TFCCHD membrane has a potential application for dye desalination process.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 12030333
2077-0375
Relation: https://www.mdpi.com/2077-0375/12/3/333; https://doaj.org/toc/2077-0375
DOI: 10.3390/membranes12030333
Access URL: https://doaj.org/article/0c061294ce3b4ad2ad7e5cf83b8d97c2
Accession Number: edsdoj.0c061294ce3b4ad2ad7e5cf83b8d97c2
Database: Directory of Open Access Journals
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More Details
ISSN:12030333
20770375
DOI:10.3390/membranes12030333
Published in:Membranes
Language:English