Enhanced catalytic degradation of 4-NP using a superhydrophilic PVDF membrane decorated with Au nanoparticles

被引:38
作者
Wu, Ziyang [1 ,2 ]
Lin, Haibo [1 ]
Wang, Yunze [1 ]
Yu, Xuemin [1 ,2 ]
Li, Jinglong [1 ]
Xiong, Zhu [1 ]
Wang, Yi [1 ]
Huang, Youju [1 ]
Chen, Tao [1 ]
Liu, Fu [1 ]
机构
[1] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Ningbo 315201, Zhejiang, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
NANOCOMPOSITE MEMBRANE; CARBON NANOTUBES; P-AMINOPHENOL; CELL-ADHESION; REDUCTION; POLYDOPAMINE; ROUTE;
D O I
10.1039/c6ra11380j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Poly(vinylidene fluoride) (PVDF) membranes have been widely applied to treat wastewater, however, the removal of toxic aromatic phenolic compounds remains a technical challenge due to the serious adsorption fouling and difficult degradation. Herein, we aimed to design a superhydrophilic PVDF membrane decorated with Au nanoparticles, which enhanced the rapid degradation of p-nitrophenol (4-NP). The superhydrophilic PVDF membrane with a micro/nano structured surface was decorated with Au nanoparticles via poly(dopamine) (PDA) as a spacer. The influences of membrane affinity (e.g. Hydrophilic Membrane (HM), micro/nano structured superhydrophilic membrane (MSiM), and micro/nano structured superhydrophobic membrane (MSoM)) on PDA deposition and the subsequent Au decoration were comprehensively investigated. The synthesized Au nanoparticles were characterized using transmission electron microscopy (TEM) and UV-vis absorption spectra. The morphology and composition was evaluated using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Static catalytic experiments demonstrated that MSiM degraded over 90% of 4-NP in 5 minutes with a kinetic reaction rate constant of 47.84 x 10(-2) min(-1) and high stability over 6 cycles. A membrane catalytic reactor (MCR) was designed to realize the continuous catalytic degradation of 4-NP with a kinetic reaction rate constant of 7 x 10(-2) min(-1).
引用
收藏
页码:62302 / 62309
页数:8
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