Graphene oxide (rGO)-metal oxide (TiO2/Fe3O4) based nanocomposites for the removal of methylene blue

被引:126
作者
Banerjee, Soma [1 ]
Benjwal, Poonam [1 ]
Singh, Milan [1 ]
Kar, Kamal K. [1 ,2 ]
机构
[1] Indian Inst Technol Kanpur, Adv Nanoengn Mat Lab, Mat Sci Programme, Kanpur 208016, Uttar Pradesh, India
[2] Indian Inst Technol Kanpur, Dept Mech Engn, Adv Nanoengn Mat Lab, Kanpur 208016, Uttar Pradesh, India
关键词
Methylene blue; Photocatalysis; TiO2; Graphene oxide; Sol-gel; ENHANCED PHOTOCATALYTIC DEGRADATION; SOL-GEL METHOD; AQUEOUS-SOLUTION; ELECTRON-TRANSFER; FACILE SYNTHESIS; VISIBLE-LIGHT; REACTIVE DYE; ADSORPTION; NANOTUBES; TIO2;
D O I
10.1016/j.apsusc.2018.01.085
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
Herein, ternary nanocomposites based on titanium dioxide, ferric oxide and reduced graphene oxide (GO) have been developed for photocatalytic degradation of methylene blue. The nanocomposites are prepared by simple sol-gel and wet assembly methods with varying weight ratio of each components to obtain efficient photocatalytic degradation. Due to the synergistic effect among the three components, a swift removal of methylene blue becomes possible under visible and UV light. The rGO-Fe3O4-TiO2 nanocomposite having composition 1:1:2 has achieved maximum degradation of methylene blue from the aqueous solution. About 99% of the dye has been removed within 6 min under UV irradiation, while in presence of visible light, 94% has been degraded from the wastewater. The enhancement of photocatalytic activity in this ternary system is attributed to the efficient separation of charge carriers from TiO2 to rGO under the exposure of light and the initiation of photo-Fenton reaction due to the incorporated Fe3O4 nanoparticles in presence of H2O2, which provides highly reactive hydroxyl ions that mineralize the pollutants. All these results indicate that these ternary nanocomposites possess great potential for both UV and visible light driven methylene blue destruction from the wastewater. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:560 / 568
页数:9
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