Electrospinning preparation of a H4SiW12O40/polycaprolactam composite nanofibrous membrane and its greatly enhanced photocatalytic activity and mechanism

被引:11
作者
Li, Wei [1 ]
Li, Tingting [1 ]
Ma, Xuegang [2 ]
Li, Yuanliang [2 ]
An, Libao [3 ]
Zhang, Zhiming [1 ]
机构
[1] North China Univ Sci & Technol, Coll Mat Sci & Engn, Hebei Prov Key Lab Inorgan Nonmetall Mat, Tangshan 063009, Peoples R China
[2] North China Univ Sci & Technol, Anal & Testing Ctr, Tangshan 063009, Peoples R China
[3] North China Univ Sci & Technol, Coll Mech Engn, Tangshan 063009, Peoples R China
来源
RSC ADVANCES | 2016年 / 6卷 / 15期
基金
中国国家自然科学基金;
关键词
AQUEOUS-SOLUTION; METHYL-ORANGE; AZO DYES; DEGRADATION; ACID; WATER; TIO2; NANOPARTICLES; IRRADIATION; POLLUTANTS;
D O I
10.1039/c5ra25550c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
H4SiW12O40/polycaprolactam (PA6) composite nanofibrous membranes with a minimum average diameter of similar to 70 nm were prepared by an electrospinning technique. Characterization with Fourier transform infrared spectroscopy (FT-IR), energy-dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) indicated that H4SiW12O40 has been successfully loaded into the PA6 membrane and its Keggin structure was intact. The as-prepared H4SiW12O40/PA6 membranes exhibited greatly enhanced photocatalytic efficiency (>= 96.0%) and excellent reusability in the degradation of methyl orange (MO) under ultraviolet irradiation, which may be attributed to the synergistic effect of PA6 and H4SiW12O40. The photocatalytic process was likely to be driven by the reductive pathway with a much faster degradation rate due to the electron donation from PA6 to H4SiW12O40. The hydrogen bonds between H4SiW12O40 and PA6 could enhance the stability of H4SiW12O40 in the membrane, so that there was nearly no loss of photocatalytic activity of the catalyst after three cycles of reactions. In view of this, H4SiW12O40/PA6 composite nanofibrous membranes exhibit potential for practical applications to eliminate organic pollutants from wastewater.
引用
收藏
页码:12491 / 12496
页数:6
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