Effect of surface hydroxyl group density of support membrane on water permeance of polyamide thin-film composite membrane

被引:1
|
作者
Matsuoka, Atsushi [1 ,2 ]
Miyake, Takefumi [1 ,2 ]
Nakagawa, Keizo [1 ,3 ]
Yoshioka, Tomohisa [1 ,3 ]
Kamio, Eiji [1 ,2 ]
Matsuyama, Hideto [1 ,2 ]
机构
[1] Kobe Univ, Res Ctr Membrane & Film Technol, 1-1 Rokkodai, Kobe 6578501, Japan
[2] Kobe Univ, Dept Chem Sci & Engn, 1-1 Rokkodai, Kobe 6578501, Japan
[3] Kobe Univ, Grad Sch Sci Technol & Innovat, 1-1 Rokkodai, Kobe 6578501, Japan
关键词
INTERFACIAL POLYMERIZATION; REVERSE-OSMOSIS; PERFORMANCE; SPECTROSCOPY; HYDROLYSIS;
D O I
10.1016/j.memsci.2024.123161
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Polyamide-based thin-film composite (TFC) membranes are widely used in water treatment processes. Recently, the influence of support membranes on the performance of polyamide layers has garnered considerable attention. Regarding the chemical properties of the support membranes, the surface wettability and the interaction between the amine monomer used for interfacial polymerization and the membrane surface are considered to play crucial roles. In this study, we investigated the effect of the wettability of the support membrane surface and its interaction with the amine monomer on the water permeance of TFC membranes. We prepared TFC membranes on polyketone support membranes with varying surface hydroxyl group densities and aqueous solution wettabilities. While no clear correlation was observed between the support membrane's wettability and the water permeance of the TFC membrane, an increase in hydroxyl group density did result in higher water permeance. The hydroxyl groups interact with PIP, inhibiting PIP diffusion and potentially leading to the formation of a thinner polyamide layer, which enhances water permeance. Therefore, the interaction between the amine monomer and support membrane surface strongly affects the formation of the polyamide layer.
引用
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页数:10
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