The ionic liquid [EMIM]OAc as a solvent to fabricate stable polybenzimidazole membranes for organic solvent nanofiltration

被引:159
作者
Xing, Ding Yu [1 ,2 ]
Chan, Sui Yung [3 ]
Chung, Tai-Shung [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 119260, Singapore
[2] Natl Univ Singapore, NUS Environm Res Inst, Singapore 119260, Singapore
[3] Natl Univ Singapore, Dept Pharm, Singapore 119260, Singapore
关键词
HOLLOW-FIBER MEMBRANES; ULTRAFILTRATION MEMBRANES; RESISTANT NANOFILTRATION; POSITRON-ANNIHILATION; NONAQUEOUS SYSTEMS; SOLUTE TRANSPORT; POLYAMIDE-IMIDE; GAS PERMEATION; SEPARATION; OSMOSIS;
D O I
10.1039/c3gc41634h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have provided two feasible methods to prepare stable organic solvent nanofiltration (OSN) membranes by chemically cross-linking the polybenzimidazole (PBI) membranes fabricated from environmentally benign ionic liquids for the first time. A glutaraldehyde (GA)-water solution and a 1,2,7,8diepoxyoctane (DEO)-n-heptane solution were employed to cross-link PBI membranes. The effects of these cross-linking agents on membrane stability and separation performance toward various solvents, including polar aprotic solvents, have been carefully examined. The GA cross-linking method, with little consumption of traditional organic solvents and energy, yielded a PBI membrane with a high and steady ethanol flux [3.69 L (m(2) bar h)(-1)] and ethyl acetate flux [5.21 L (m(2) bar h)(-1)]. Although PBI membranes cross-linked by DEO showed lower ethanol and ethyl acetate fluxes, they displayed impressive stability in aggressive solvents such as dimethyl sulfoxide (DMSO), N-methyl-2-pyrrolidinone (NMP) and N, N-dimethylacetamide (DMAc). Overall, PBI membranes cross-linked by both agents exhibited reasonable rejections which varied slightly from solvent to solvent due to different solute-solvent-membrane interactions. This study not only offers a new range of membrane materials and fabrication approaches for OSN, but will also enhance membrane-based green technology for the recovery of organic solvents.
引用
收藏
页码:1383 / 1392
页数:10
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