三醋酸纤维素
正渗透
膜
薄膜复合膜
聚酰胺
化学工程
界面聚合
图层(电子)
逐层
材料科学
反渗透
聚合
选择性
色谱法
化学
高分子化学
聚合物
纳米技术
复合材料
有机化学
单体
生物化学
催化作用
工程类
作者
Soon Bum Kwon,Seongpil Jeong,Seungkwan Hong,Seockheon Lee
出处
期刊:Desalination
[Elsevier BV]
日期:2024-01-01
卷期号:570: 117067-117067
标识
DOI:10.1016/j.desal.2023.117067
摘要
The internal concentration polymerization (ICP) phenomenon may hinder the flux of forward osmosis (FO) membranes. The mitigation of ICP can be achieved by employing a porous support layer structure. Nevertheless, conventional interfacial polymerization (IP) methods encounter challenges in establishing a dense selective layer upon a highly porous support layer. In this study, the support-free assembled molecular layer-by-layer (SF-mLbL) was suggested to manufacture the thin-film composite (TFC) membrane by combining the separately fabricated polyamide (PA) selective layer with a tunable thickness and the highly porous support layer. The SF-mLbL (8 wt%) membrane had a higher water flux and selectivity (43.52 ± 0.89 LMH/0.15 ± 0.01 g L−1) than those (10.34 ± 0.48 LMH/0.75 ± 0.02 g L−1 and 7.41 ± 0.18 LMH/0.81 ± 0.01 g L−1) of IP-PA and commercial cellulose triacetate membranes as 0.5 M NaCl draw solution in FO mode. Consequently, the SF-mLbL membranes exhibited significant improvement in the FO process with well-balanced permselectivity.
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