A thin film nanocomposite reverse osmosis membrane containing amine-functionalized carbon nanotubes

被引:107
|
作者
Vatanpour, Vahid [1 ]
Safarpour, Mahdie [2 ]
Khataee, Alireza [2 ,3 ]
Zarrabi, Hamed [1 ]
Yekavalangi, Mohammad Ehsan [1 ]
Kavian, Mostafa [1 ]
机构
[1] Kharazmi Univ, Fac Chem, Tehran 1571914911, Iran
[2] Univ Tabriz, Fac Chem, Dept Appl Chem, Res Lab Adv Water & Wastewater Treatment Proc, Tabriz 5166614766, Iran
[3] Near East Univ, Dept Mat Sci & Nanotechnol Engn, TR-99138 North Cyprus 10, Mersin, Turkey
基金
美国国家科学基金会;
关键词
Reverse osmosis; Desalination; Carbon nanotube; Nanostructured membrane; REDUCED GRAPHENE OXIDE/TIO2; NANOFILTRATION MEMBRANE; SEAWATER DESALINATION; SURFACE MODIFICATION; ANTIFOULING PROPERTIES; POLYAMIDE; PERFORMANCE; NANOPARTICLES; FABRICATION; COMPOSITES;
D O I
10.1016/j.seppur.2017.04.038
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Thin film composite reverse osmosis (RO) membranes were fabricated by interfacial polymerization of m-phenylenediamine and trimesoyl chloride monomers and modified with amine-functionalized multi-walled carbon nanotubes (MWCNT-NH2), which dispersed in amine solution. The surface characteristics of the prepared membranes were studied by scanning electron microscopy (SEM), atomic force microscopy (AFM) and contact angle analysis. The desalination performance of the membranes was investigated in terms of water flux and NaCl rejection. The hydrophilicity and permeability of the modified membranes were increased without any reduction in their salt rejection. The fouling resistance of the membranes was evaluated by their flux decrement through filtration of bovine serum albumin (BSA) solution and water flux recovery ability after the fouling. The incorporating of MWCNT-NH2 into polyamide layer of RO membranes improved their fouling resistance by reducing surface roughness and increasing negative charge and hydrophilicity of the membrane surface. The membrane containing 0.002 wt% MWCNT-NH2 presented the best desalination and antifouling performance. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 143
页数:9
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