Mechanically and structurally robust sulfonated block copolymer membranes for water purification applications

被引:14
|
作者
Yeo, J. [1 ]
Kim, S. Y. [2 ]
Kim, S. [3 ]
Ryu, D. Y. [4 ]
Kim, T-H [5 ]
Park, M. J. [1 ,2 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Dept Chem, Pohang 790784, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Div Adv Mat Sci WCU, Pohang 790784, South Korea
[3] Res Inst Ind Sci & Technol RIST, Energy & Environm Res Div, Pohang 790330, South Korea
[4] Yonsei Univ, Dept Chem & Biomol Engn, Seoul 120749, South Korea
[5] Korea Atom Energy Res Inst, Div Neutron Sci, Taejon 305353, South Korea
基金
新加坡国家研究基金会;
关键词
POLY(ARYLENE ETHER SULFONE); NANOFILTRATION MEMBRANE; COMPOSITE MEMBRANES; CROSS-LINKING; TRANSPORT; SEPARATION; ROUGHNESS; BEHAVIOR; KETONE); SURFACE;
D O I
10.1088/0957-4484/23/24/245703
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The effective removal of ionic pollutants from contaminated water using negatively charged nanofiltration membranes is demonstrated. Block copolymers comprising polystyrene (PS) and partially hydrogenated polyisoprene (hPI) were synthesized by varying chain architectures. A one step procedure of cross-linking (hPI blocks) and sulfonation reactions (PS chains) was then carried out, which was revealed as an effective method to enhance mechanical integrity of membranes while hydrophilic sulfonated chains remain intact. In particular, the control of chain architecture allows us to create a synergetic effect on optimizing charge densities of the membrane, water permeability, and mechanical integrity under water purification conditions. The best performing membrane can almost completely (>99%) reject various divalent cations and also show NO3- rejection >85% and Na+ rejection >87%. Well defined nanostructures (tens of nanometers) as well as the periodically arranged water domains (a few nanometers) within hydrophilic phases of the hydrated membranes were confirmed by in situ neutron scattering experiments.
引用
收藏
页数:11
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