Freestanding hematite nanofiber membrane for visible-light-responsive photocatalyst

被引:12
|
作者
Sittirug, Ing-orn [1 ]
Ksapabutr, Bussarin [1 ,2 ]
Panapoy, Manop [1 ,2 ]
机构
[1] Silpakorn Univ, Fac Engn & Ind Technol, Dept Mat Sci & Engn, Nakhon Pathom 73000, Thailand
[2] Chulalongkorn Univ, Ctr Excellence Petrochem & Mat Technol, High Performance & Smart Mat, Bangkok 10330, Thailand
关键词
alpha-Fe2O3; Electrospinning; Sol-gel process; Nanofiber membrane; Photocatalysis; PHOTOELECTROCHEMICAL PROPERTIES; TIO2; NANOPARTICLES; DEGRADATION; DYE; PERFORMANCE; FE2O3; OXIDE; CATALYST; ACID; ZRO2;
D O I
10.1016/j.ceramint.2015.11.051
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Freestanding mesoporous hematite (alpha-Fe2O3) nanofiber membranes were successfully fabricated by sol gel electrospinning process using ferratrane precursor for use as a high-performance material for visible-light-responsive photocatalyst. Non-porous nanofiber membranes spun on the heated collector at 300 degrees C were crystalline alpha-Fe2O3 phase. Upon calcination, pure mesoporous nanofiber membranes were obtained even at a low temperature of 400 degrees C. The photocatalytic membrane calcined at 400 degrees C showed the highest efficiency for methylene blue (MB) degradation under visible-light irradiation. The synergetic effects of higher surface area, pore volume and pore diameter promoted the photocatalytic efficiency for MB degradation under visible light. The utilisation of photocatalyst in the form of membrane could not only solve the problems of catalyst separation and recovery, but also produce high photodegradation efficiency for both systems without and with hydrogen peroxide even at a catalyst loading as low as 0.04 g/L. No appreciable loss in photocatalytic activity was observed and structural integrity was retained, even after five cycles of photodegradation, which predicted the stability and reusability of these nanofiber membranes for practical use in environmental applications. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:3864 / 3875
页数:12
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