膜
界面聚合
聚偏氟乙烯
化学工程
浓差极化
材料科学
薄膜复合膜
聚酰胺
缓压渗透
正渗透
反渗透
相位反转
基质(水族馆)
纳滤
微滤
色谱法
单体
高分子化学
聚合物
复合材料
化学
生物化学
海洋学
工程类
地质学
作者
Yuzhe Zhou,Yuqing Shi,Danrong Cai,Wentao Yan,Zhou Yong,Congjie Gao
标识
DOI:10.1016/j.memsci.2023.122165
摘要
Macroporous substrates have great potential in the development of high performance thin film composite forward osmosis (TFC FO) membranes. This paper reports on the preparation of TFC FO membrane via support-free interfacial polymerization (SFIP) technology on a macroporous substrate. SFIP technology can effectively break the bottleneck of conventional interfacial polymerization (IP) technology, which makes it difficult to form a complete polyamide (PA) film on the macroporous substrate. Briefly, the complete PA film is formed at the free water-organic phase interface and then attached to the macroporous substrate by vacuum filtration. The monomer concentration and filtration pressure were adjusted to form the optimal SFIP-PA film. Meanwhile, we chose a macroporous polyvinylidene fluoride (PVDF) microfiltration substrate and screened the pore size to reduce the structural parameters and then the internal concentration polarization, which caused the improvement of water flux. The performance of SFIP-PVDF membranes was investigated and discussed. Under the AL-FS mode with DI water and 1.0 M NaCl solution as the feed solution and draw solution, respectively, the SFIP-PVDF membrane, which used a macroporous PVDF substrate with a pore size of 0.45 μm exhibited a water flux (20 L/m2•h) and a reverse salt flux (2.5 g/m2•h). Besides, the membrane showed good stability in the 72 h test. The specific salt flux (JS/JW) of SFIP-PVDF membranes was much lower than that of IP-PVDF membranes prepared via IP technology, which were incomplete and defective, suggesting that SFIP technology was superior to IP technology. This work effectively exploits the potential of macroporous substrates for the development of high performance TFC FO membranes and provides an insight into the high performance FO membrane design.
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