Preparation of Thin Film Nanocomposite Membranes with Surface Modified MOF for High Flux Organic Solvent Nanofiltration

被引:127
作者
Guo, Xiangyu [1 ]
Liu, Dahuan [1 ]
Han, Tongtong [1 ]
Huang, Hongliang [1 ]
Yang, Qingyuan [1 ]
Zhong, Chongli [1 ]
机构
[1] Beijing Univ Chem Technol, Dept Chem Engn, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
关键词
metal-organic framework; surface modification; thin film nanocomposite membrane; interfacial polymerization; organic solvent nanofiltration; MIXED-MATRIX MEMBRANES; RESISTANT NANOFILTRATION; INTERFACIAL POLYMERIZATION; COMPOSITE MEMBRANES; REVERSE-OSMOSIS; PERVAPORATION DEHYDRATION; PHARMACEUTICAL-INDUSTRY; SILICA NANOPARTICLES; MOLECULAR SEPARATION; CO2/CH4; SEPARATION;
D O I
10.1002/aic.15508
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Preparation of defect-free and optimized thin film nanocomposite (TFN) membranes is an effective way to enhance the process of organic solvent nanofiltration. However, it still remains a great challenge due to poor filler particle dispersibility in organic phase and compatible issue between fillers and polymers. Aiming at these difficulties, UiO-66-NH2 nanoparticles were surface modified with long alkyl chains and used in the preparation of TFN membranes. As a result, defect-free TFN membranes with ultrathin MOF@ polyamide layer were successfully prepared benefited from the improved particle dispersibility in n-hexane. Significant enhancement was found in methanol permeance after nanoparticle incorporation, without comprising the tetracycline rejection evidently. Especially, the novel TFN membrane prepared with organic phase solution containing 0.15% (w/v) modified UiO-66-NH2 nanoparticles showed a superior methanol permeance of 20 L center dot m(-2)center dot h(-1)center dot bar(-1) and a tetracycline rejection of about 99%, which is appealing to the application in pharmaceutical industry for example. (C) 2016 American Institute of Chemical Engineers AIChE J, 63: 1303-1312, 2017
引用
收藏
页码:1303 / 1312
页数:10
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