Enhancement of Flux and Solvent Stability of Matrimid® Thin-Film Composite Membranes for Organic Solvent Nanofiltration

被引:112
|
作者
Sun, Shi-Peng [1 ,2 ]
Chung, Tai-Shung [1 ,2 ]
Lu, Kang-Jia [1 ]
Chan, Sui-Yung [3 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 119260, Singapore
[2] Natl Univ Singapore, NUS Environm Res Inst, Singapore 117411, Singapore
[3] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
关键词
organic solvent nanofiltration; polyimide; Matrimid((R)); thin-film composite membrane; interfacial polymerization; stability; HOLLOW-FIBER MEMBRANES; ATOMIC-FORCE MICROSCOPY; CROSS-LINKING; INTERFACIAL POLYMERIZATION; RESISTANT NANOFILTRATION; POLYIMIDE MEMBRANES; REVERSE-OSMOSIS; (OSN)-INTERFACIAL POLYMERIZATION; PERVAPORATION DEHYDRATION; SEPARATION PERFORMANCE;
D O I
10.1002/aic.14558
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The development of high flux and solvent-stable thin-film composite (TFC) organic solvent nanofiltration (OSN) membranes was reported. A novel cross-linked polyimide substrate, consisting of a thin skin layer with minimum solvent transport resistance and a sponge-like sublayer structure that could withstand membrane compaction under high-pressure was first fabricated. Then the solvent flux was significantly enhanced without compromising the solute rejection by the coupling effects of (1) the addition of triethylamine/camphorsulfonic acid into the monomer solution, and (2) the combined post-treatments of glycerol/sodium dodecyl sulphate immersion and dimethyl sulfoxide (DMSO) filtration. Finally, the long-term stability of the TFC membrane in aprotic solvents such as DMSO was improved by post-crosslink thermal annealing. The novel TFC OSN membrane developed was found to have superior rejection to tetracycline (MW: 444 g/mol) but was very permeable to alcohols such as methanol (5.12 lm(-2)h(-1)bar(-1)) and aprotic solvents such as dimethylformamide (3.92 lm(-2)h(-1)bar(-1)) and DMSO (3.34 lm(-2)h(-1)bar(-1)). (c) 2014 American Institute of Chemical Engineers AIChE J, 60: 3623-3633, 2014
引用
收藏
页码:3623 / 3633
页数:11
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