Surface modification of thin film composite membrane support layers with polydopamine: Enabling use of reverse osmosis membranes in pressure retarded osmosis

被引:278
作者
Arena, Jason T. [1 ,2 ]
McCloskey, Bryan [3 ]
Freeman, Benny D. [4 ]
McCutcheon, Jeffrey R. [1 ,2 ]
机构
[1] Univ Connecticut, Dept Chem Mat & Biomol Engn, Storrs, CT 06269 USA
[2] Univ Connecticut, Ctr Environm Sci & Engn, Storrs, CT 06269 USA
[3] IBM Almaden Res Ctr, San Jose, CA 95120 USA
[4] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
Forward osmosis; Pressure retarded osmosis; Thin film composite membrane; Engineered osmosis; Polydopamine; Hydrophilicity; Membrane modification; INTERNAL CONCENTRATION POLARIZATION; HOLLOW-FIBER MEMBRANES; AMMONIA-CARBON DIOXIDE; WATER FLUX; SEA-WATER; DESALINATION; POLYMERIZATION; CHEMISTRY; DOPAMINE; COATINGS;
D O I
10.1016/j.memsci.2011.01.060
中图分类号
TQ [化学工业];
学科分类号
081705 [工业催化];
摘要
Previous investigations of forward osmosis and pressure retarded osmosis identified asymmetric membrane support layer hydrophilicity as critical to obtain high water flux. In this study, the support layers of two commercially available thin film composite reverse osmosis membranes were modified to enhance their hydrophilicity. The membrane support layers were coated with polydopamine, a novel bio-inspired hydrophilic polymer. This resulted in increased hydrophilicity and a corresponding increase in 'wetted porosity' and reduced internal concentration polarization. The modified membranes were then characterized for contact angle, salt rejection, hydraulic permeability, salt flux, and osmotic flux. The results were promising, indicating that the modified reverse osmosis membranes exhibited an eight to fifteen fold increase in flux performance under test conditions when compared to baseline control data. This modification method, which is scalable, has the potential to enable the use of existing thin film composite membranes for all engineered osmosis applications. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 62
页数:8
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