Development of composite membranes with irregular rod-like structure via atom transfer radical polymerization for efficient oil-water emulsion separation

被引:75
作者
Cui, Jiuyun [1 ]
Xie, Atian [2 ]
Zhou, Shi [4 ]
Liu, Siwei [1 ]
Wang, Qianqian [2 ]
Wu, Yilin [2 ]
Meng, Minjia [2 ]
Lang, Jihui [3 ]
Zhou, Zhiping [1 ]
Yan, Yongsheng [2 ]
机构
[1] Jiangsu Univ, Sch Mat Sci & Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Sch Chem & Chem Engn, Inst Green Chem & Chem Technol, Zhenjiang 212013, Peoples R China
[3] Jilin Normal Univ, Coll Phys, Siping 136000, Peoples R China
[4] Jiangsu Chengxiang New Mat Technol Co LTD, Nantong, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Composite membrane; ATRP; Flux recovery; Oil-water emulsions separation; Acrylamide; PVDF MEMBRANES; INORGANIC MEMBRANES; INSPIRED METHOD; OIL/WATER; NANOSHEETS; DESIGN; SUPERHYDROPHILICITY; PERFORMANCE; FABRICATION; CELLULOSE;
D O I
10.1016/j.jcis.2018.08.055
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
Development of superhydrophilic, stable and cost-effective composite membranes for efficient oil-water emulsion separation is highly desirable. Herein, an irregular rod-like composite membrane was prepared through 3-aminopropyltriethoxysilane (APTES) modification, followed by acrylamide polymerization with atomic transfer radical polymerization (ATRP). The as-prepared membrane exhibits superhydrophilicity/underwater superoleophobicity due to its irregular rod-like structure and poresinduced capillary actions. The composite membrane has demonstrated sufficient stability in acidic, alkaline and salty environments due to the polymerization of acrylamide. Moreover, the as-prepared composite membrane has effectively separated various oil-water emulsions and demonstrated high permeation and superior flux recovery. The present work demonstrates that the ATRP-assisted composite membrane is a promising material in a wide range of applications, such as industrial wastewater recovery and drinking water treatment. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:278 / 286
页数:9
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