Fabrication of mesoporous TiO2 membranes by a nanoparticle-modified polymeric sol process

被引:26
作者
Li, Dan [1 ]
Wang, Hui [1 ]
Jing, Wenheng [1 ]
Fan, Yiqun [1 ]
Xing, Weihong [1 ]
机构
[1] Nanjing Tech Univ, Coll Chem & Chem Engn, Natl Engn Res Ctr Special Separat Membrane, State Key Lab Mat Oriented Chem Engn, Nanjing, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Mesoporous membrane; Titania; Nanoparticle doping; TiO2; membrane; COMPOSITE MEMBRANES; GEL PROCESS; CRYSTALLIZATION KINETICS; TOUGHENING MECHANISMS; EPOXY POLYMERS; PART; ALUMINA; FRACTURE; NANOFILTRATION; NANOCOMPOSITES;
D O I
10.1016/j.jcis.2014.05.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A straightforward synthesis of crack-free mesoporous titania membrane on a macroporous support without intermediate layers by a nanoparticle-modified polymeric sol-gel process is reported. TiO2 nanoparticle (Degussa P25) was dispersed into the prepared sol to toughen the formed gel. This helped to avoid the cracking of membrane during the drying and early stage of sintering, particularly when the sol-gel transformation occurred on a substrate with an uneven surface. The results of X-ray diffraction and Brunauer-Emmett-Teller analyses show that the nanoparticle doping did not significantly affect the particle size of TiO2 nanocrystals; however, it slightly broadened the pore size distribution because it has a larger particle size compared to the prepared materials. The sols with and without P25 nanopartide were subsequently dip-coated on a support with average pore size of 150 nm, thus formed a mesoporous membrane layer after drying and sintering processes. An integrated, crack-free mesoporous TiO2 membrane layer was obtained by this method, while the membrane prepared with the original sol developed a few cracks. Further, the filtration experiment showed that the prepared membrane had a high flux, and the membrane with nanoparticle modification delivered better separation performance by rejection of dextran. (C) 2014 Published by Elsevier Inc.
引用
收藏
页码:43 / 48
页数:6
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