High permeate flux of PVA/PSf thin film composite nanofiltration membrane with aluminosilicate single-walled nanotubes

被引:82
作者
Barona, Garry Nathaniel B. [1 ]
Choi, Mijin [1 ]
Jung, Bumsuk [1 ]
机构
[1] Myongji Univ, Dept Environm Engn & Energy, Lab Environm & Energy Mat, Yongin 449728, Gyeonggi Do, South Korea
关键词
Thin film nanocomposite; Aluminosilicate single-walled nanotube; Poly(vinyl alcohol); High permeate flux nanofiltration membrane; REVERSE-OSMOSIS; INTERFACIAL PROPERTIES; SYNTHETIC IMOGOLITE; POLYVINYL-ALCOHOL; PERFORMANCE; PURIFICATION; RETENTION; SIZE;
D O I
10.1016/j.jcis.2012.07.049
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new type of thin film nanocomposite (TFN) membranes for nanofiltration was successfully prepared by incorporating aluminosilicate single-walled nanotubes (SWNTs) within the poly(vinyl alcohol) (PVA) matrix. The nanocomposite PVA film was composed of well dispersed synthesized aluminosilicate SWNT with up to 20% volume fraction cast on a polysulfone support. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) revealed that the TFN membranes have characteristic bands at 920-1010 cm(-1) corresponding to Si-OH and Si-O-Al stretching vibration of the aluminosilicate SWNT. This insinuated the successful incorporation of aluminosilicate SWNT into the polymer matrix, which was further confirmed and quantified by X-ray photoelectron spectroscopy (XPS). The PVA layers, in the range of 0.99-1.36 mu m, are free from large defects or cracks as observed in the scanning electron microscopy (SEM) images. The membrane surface hydrophilicity increased as the membrane roughness decreased and as the contact angles decreased from 64.2 degrees to 59.4-50.5 degrees. The increase in water flux is due to the presence of hydrophilic nanotubes. With the incorporation of the aluminosilicate single-walled nanotubes, higher permeate water flux was achieved, while sustaining high rejection of divalent ions (97%) and monovalent ions (59%). (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:189 / 197
页数:9
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