Polysulfone Membranes via Thermally Induced Phase Separation附视频

被引:0
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作者
Hongqing Liang [1 ,2 ]
Haonan Li [1 ,2 ]
Haohao Yu [1 ,2 ]
Yongting Zhou [1 ,2 ]
徐志康 [1 ,2 ]
机构
[1] Key Laboratory of Macromolecular Synthesis and Functionalizationof the Ministry of Education, Department of Polymer Science and Engineering, Zhejiang University
[2] Key Laboratory of Adsorption and Separation Materials & Technologies of Zhejiang Province, Department of Polymer Science and Engineering, Zhejiang
关键词
Polysulfone membrane; Pore structure; Diphenyl sulfone; Polyethylene glycol; Thermally induced phase separation;
D O I
暂无
中图分类号
O633.3 [链上含硫的聚合物]; TB383.2 [];
学科分类号
摘要
Polysulfone(PSF) membranes have gained great attention in the fields of ultrafiltration, microfiltration, and thin film composite membranes for nanofiltration or reverse osmosis. For the first time, it is proposed to fabricate PSF membranes via thermally induced phase separation(TIPS) process using diphenyl sulfone(DPSO2) and polyethylene glycol(PEG) as mixed diluent. DPSO2 is chosen as a crystallizable diluent, while PEG isconsidered in terms of molecular weight(Mw) and dosage. We systematically investigate the interactions between PSF, DPSO2 and PEG based on thesimulation calculations and solubility parameter theory. It is inferred that DPSO2 has an excellent compatibility with PSF, and the addition of PEG results in the ternary system thermodynamically less stable and then facilitates its liquid-liquid(L-L) phase separation.SEM images indicate that cellular-like pores are obvious throughout the membrane when the PEG content in the mixed diluent is 25wt%-35 wt%. We can facilely manipulate the pore size, water flux and mechanical properties of PSF membranes with the dosage of PEG-200, the Mwof PEG or the cooling rate. The successful application of TIPS can provide a new approach for structure manipulation and performance enhancement of PSF membranes.
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页码:846 / 856
页数:11
相关论文
共 2 条
  • [1] Matsuyama H,Ohga K,Maki T,et al. J.Appl.Polym.Sci . 2003
  • [2] Yang,Y,Zhang,H,Wang,P,Zheng,Q,Li,J. J.Membr.Sci . 2007