Preparation and properties of polyamide/titania composite nanofiltration membrane by interfacial polymerization

被引:38
|
作者
Wang, Qiao [1 ,2 ]
Zhang, Guang-shan [2 ]
Li, Zhan-shuang [1 ]
Deng, Sheng [2 ]
Chen, Han [2 ]
Wang, Peng [2 ]
机构
[1] Harbin Engn Univ, Coll Mat Sci & Chem Engn, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, Sch Municipal & Environm Engn, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
基金
美国国家科学基金会;
关键词
Interfacial polymerization; Polyamide; Nanofiltration membrane; Titania; TRIMESOYL CHLORIDE TMC; REVERSE-OSMOSIS; ULTRAFILTRATION MEMBRANE; POLYVINYLAMINE PVAM; NANOPARTICLES;
D O I
10.1016/j.desal.2014.08.001
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The TiO2 sot was added in the polysulfone (PSF) casting membrane solution to prepare polysulfone/titania hybrid membrane in this work. Then the polypiperazine-amide composite nanofiltration (NF) membranes were prepared on PSF/TIO2 hybrid membranes by interfacial polymerization. Piperazine and trimesoyl chloride were used as monomers in aqueous phase and organic phase, respectively. Different preparation conditions affecting the separation performances of NF membrane were discussed, including TiO2 sol concentration, piperazine concentration, trimesoyl chloride concentration, and reaction time. The chemical structure characterizations of polyamide composite membrane were tested by attenuated total reflectance infrared (ATR-IR). The surface images and cross sections were observed by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The addition of TiO2 sol changed the salt rejection slightly, but the water flux was three times than that of the polyamide membrane on the PSF support membrane. The polyamide NF membrane prepared under the optimum condition exhibited Na2SO4 rejection of 96.94% and water flux of 12.84 L m(-2) h(-1). According to the intercepting experiments of polyethylene glycols, the molecular weight cut-off (MWCO) of the resulting membrane was under 600 Da. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 44
页数:7
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