High performance ceramic hollow fiber supported PDMS composite pervaporation membrane for bio-butanol recovery

被引:140
作者
Dong, Ziye [1 ]
Liu, Gongping [1 ]
Liu, Sainan [1 ]
Liu, Zhengkun [1 ]
Jin, Wanqin [1 ]
机构
[1] Nanjing Univ Technol, Coll Chem & Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Ceramic hollow fiber; Polydimethylsiloxane; Composite membrane; Pervaporation; Butanol recovery; DILUTE AQUEOUS-SOLUTIONS; HIGH-FLUX; ABE FERMENTATION; WATER MIXTURES; ETHANOL ABE; SEPARATION; ACETONE; MODEL; ALCOHOLS; LAYER;
D O I
10.1016/j.memsci.2013.08.039
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this work, ceramic hollow fiber supported polydimethylsiloxane (PDMS) composite membranes were developed by dip-coating PDMS layer on the surface of macroporous ceramic hollow fiber support. By controlling the properties of polymer solution and ceramic hollow fiber, high-quality ceramic hollow fiber supported PDMS composite membranes were fabricated for pervaporation (PV) recovery of bio-butanol. It was found both the viscosity of PDMS dip-coating solution and pore size and structure of ceramic support played critical roles in determining the microstructures, the mass transport and the PV performance of PDMS composite membrane. The optimized composite membrane with detect-free PDMS layer and low transport resistance of support showed a total flux of 1282 g/m(2) h and separation factor of 42.9 for 1 wt% n-butanol-water mixtures at temperature of 40 degrees C during 200 h continuous operation. In addition, the membrane PV performance and stability in acetone-butanol-ethanol (ABE) fermentation broth were investigated. The results showed the PDMS composite membrane exhibited high and stable performance for butanol recovery from ABE systems. Compared with literatures, our work demonstrated that the ceramic hollow fiber supported PDMS composite membrane could be a competitive PV membrane for recovering organic compounds from fermentation broth to produce renewable biofuels. (C) 2013 Elsevier B.V. All rights reserved
引用
收藏
页码:38 / 47
页数:10
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