Effect of solvents on performance of polyethersulfone ultrafiltration membranes: Investigation of metal ion separations

被引:91
|
作者
Arthanareeswaran, G. [1 ]
Starov, Victor M. [2 ]
机构
[1] Natl Inst Technol, Dept Chem Engn, Membrane Res Lab, Tiruchirappalli 620015, India
[2] Univ Loughborough, Dept Chem Engn, Loughborough LE11 3TU, Leics, England
关键词
Ultrafiltration; Polyethersulfone; Solvents; Liquid-phase polymer-based retention; Removal of metal ions; CELLULOSE-ACETATE; BINDING; ACID;
D O I
10.1016/j.desal.2010.09.006
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The new polyethersulfone (PES) based ultrafiltration membranes were formed using a two stage process of dry and wet phase inversion in non solvent coagulation bath. The effects of three different solvents such as, N, N-dimethylformamide (DMF), N-methyl-2-pyrrolidone (NMP) and Dimethyl sulphoxide (DMSO) of 82.5% and 85% concentrations on the performance of final membranes were extensively investigated. Scanning electron microscopy (SEM) image results proved that PES membranes with an asymmetric structure were successfully formed. The number of pores formed on the top layer of PES membranes using above-mentioned three solvents was the result of the combined effect of the thermodynamic properties of the system (composition, concentrations, and phase behaviour) and membrane formation kinetics, whereas, the formation of the macroporous sub layer of those membranes was controlled by the diffusion rate of solvent-nonsolvent. The flux of pure water, membrane resistance, mechanical stability, molecular weight cut-off (MWCO) and separation performance of the PES membranes were studied. Separation of metal ions from aqueous solutions was studied for Ni(II), Cu(II) and Cr(III) using two complexing polymer ligands: polyvinyl alcohol (PVA) and poly(diallyldimethylammonium chloride) (PDDA). The separation and permeate rate (flux) efficiencies of the new membranes are compared using different solvents and different PES/solvent compositions. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 63
页数:7
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