Effect of casting solvent on the morphology and performance of sulfonated polyethersulfone membranes

被引:116
|
作者
Guan, R
Dai, H
Li, CH
Liu, JH
Xu, J
机构
[1] Hubei Univ, Coll Chem & Mat Sci, Wuhan 430062, Peoples R China
[2] Shenzhen Univ, Normal Coll, Shenzhen 518060, Peoples R China
[3] Hubei Univ, Coll Chem & Mat Sci, Wuhan 430062, Peoples R China
关键词
sulfonated polyethersulfone; casting solvent; proton exchange membrane;
D O I
10.1016/j.memsci.2005.10.025
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Sulfonated polyethersulfone (SPES) membranes were prepared using dimethylformamide (DMF), dimethylacetamide (DMAc) and N-methyl-2-pyrrolidone (NMP) as casting solvents, referred as SPES-DMF, SPES-DMAc and SPES-NMP membranes, respectively. Comprehensive and comparative studies have shown that casting solvents have significant effects on the morphology and performance of SPES membranes. The H-1 NMR spectra revealed the formation of strong hydrogen bonding between residual DMF and SPES, accompanying the thermal decomposition of DMF during the membrane preparation. The X-ray diffraction indicated a more perturbed randomness of amorphous inside of the SPES-DMF membranes than other two membranes. Atomic force microscope demonstrated different surface morphologies of three solvent cast SPES membranes, which appeared to be governed by solvent volatility combined with solvent-polymer interactions. A more co-continuous hydrophilic cluster-like structure was observed on the surface of SPES-DMAc membranes. The SPES-DMF membranes exhibited relatively low ionic exchange capacity, water uptake and large contact angle compared to the SPES-DMAc and SPES-NMP membranes. The SPES-DMAc membranes achieved the highest conductivity values at room temperature among the three membranes. These resulting differences were tentatively correlated with the different degrees of interaction between the SPES and solvents. Moreover, the conductivity differences seemed to be correlated to the morphological differences. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:148 / 156
页数:9
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