Development of nanosilver and multi-walled carbon nanotubes thin-film nanocomposite membrane for enhanced water treatment

被引:290
作者
Kim, Eun-Sik [1 ]
Hwang, Geelsu [1 ]
El-Din, Mohamed Gamal [1 ]
Liu, Yang [1 ]
机构
[1] Univ Alberta, Dept Civil & Environm Engn, Edmonton, AB T6G 2W2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Nanosilver; Carbon nanotubes; Thin-film nanocomposite; Membrane; Biofouling; SILVER NANOPARTICLES; REVERSE-OSMOSIS; FABRICATION; POLYAMIDE; NANOFILTRATION; PERMEABILITY; POLYSULFONE; SEPARATION; CHEMISTRY; MATRIX;
D O I
10.1016/j.memsci.2011.11.041
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A new type of thin-film nanocomposite (n-TFN) membrane was synthesized by the interfacial polymerization of a support layer containing acid modified multi-walled carbon nanotubes (MWNTs) and a thin-film layer containing nanosilver (nAg) particles. Microscopic characterization confirmed that MWNTs and nAg particles were distributed in the support layer and the thin-film layer, respectively. Spectroscopic characterization revealed the surface functionalities of the MWNT support layer, and nAg crystallinity and bonding components of the thin-film layer. MWNTs at 5.0 wt.% in the support layer and nAg particles at 10 wt.% in the thin-film layer enhanced the pure water permeability of the n-TFN membrane by 23% and 20%, respectively, compared to 0 wt.% of these components in their respective layers. Increases in pure water permeability and hydrophilicity of the n-TFN membrane were attributed to the diffusive effect of nanopores in the MWNTs. Salt (NaCl, Na2SO4) rejections of the n-TFN membrane were similar to thin-film composite membranes without nAg particles. Pseudomonas aeruginosa PAO1 batch tests indicated greater anti-adhesive and antibacterial properties of the n-TFN membrane compared to similar membranes without nAg particles. This study demonstrated that the acid modified MWNTs and nAg particles enhance the permeability and anti-biofouling properties of thin-film nanocomposite membranes. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 48
页数:12
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