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Extreme pH-Resistant, Highly Cation-Selective Poly(Quaternary Ammonium) Membranes Fabricated via Menshutkin Reaction-Based Interfacial Polymerization

Authors
Jeon, SungkwonKim, HansooChoi, JuyeonKim, Jeong F.Park, Ho BumLee, Jung-Hyun
Issue Date
May-2023
Publisher
WILEY-V C H VERLAG GMBH
Keywords
cation separations; interfacial polymerization; Menshutkin reaction; nanofiltrations; pH resistance; quaternary ammonium-based polymers; thin-film composite membranes
Citation
ADVANCED FUNCTIONAL MATERIALS, v.33, no.22, pp.1 - 10
Indexed
SCIE
SCOPUS
Journal Title
ADVANCED FUNCTIONAL MATERIALS
Volume
33
Number
22
Start Page
1
End Page
10
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/191060
DOI
10.1002/adfm.202300183
ISSN
1616-301X
Abstract
Membrane-based separation technologies have attracted significant interest from various industries owing to their high process efficiency. However, the wider applications of conventional polyamide (PA) thin-film composite (TFC) membranes are limited by their poor pH stability and low cation selectivity, necessitating the development of membranes with advanced chemistries. Herein, an extreme pH-resistant, highly cation-selective TFC membrane is fabricated by synthesizing a crosslinked poly(quaternary ammonium) (PQA) selective layer on a polyethylene support via Menshutkin reaction-based interfacial polymerization (Men-IP). The Men-IP process produces a thin, densely crosslinked, and positively charged PQA permselective layer without hydrolysis-prone functional groups. The fabricated PQA membrane features a highly selective molecular density that significantly exceeds those of previously reported membranes with non-PA chemistries. Moreover, the PQA membrane exhibits remarkably high rejection (>90%) and selectivity for divalent cations owing to the exceptionally strong positive charge imparted by its abundant cationic QA groups. More importantly, the PQA membrane displays ultrahigh pH stability under both extremely acidic (1.5 m H2SO4) and alkaline (5 m NaOH) conditions for 28 days. No other membrane reported in the literature demonstrates such excellent pH stability. This strategy opens a new route for fabricating highly selective membranes that can be used in harsh pH environments.
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