TiO2/EDTA-rich carbon composites: Synthesis, characterization and visible-light-driven photocatalytic reduction of Cr(VI)

被引:33
|
作者
Luo, Zhijun [1 ,2 ,3 ]
Qu, Lingling [1 ]
Jia, Jianzhong [1 ]
Wang, Jing [1 ]
Jiang, Suying [2 ,3 ]
Wu, Zhiren [1 ,2 ,3 ]
Wu, Xiangyang [1 ]
机构
[1] Jiangsu Univ, Zhenjiang 212013, Peoples R China
[2] Environm Protect Dept Jiangsu Prov, Engn Technol Ctr Heavy Met Wastewater Treatment &, Yixing 214200, Peoples R China
[3] Jiangsu ATK Environm Engn Design & Res Inst Co Lt, Yixing 214200, Peoples R China
关键词
TiO2; Carbon-based materials; Nanostructures; Photocatalysis; Reduction of Cr(VI); HEAVY-METAL TOXICITY; DOPED TIO2; DEGRADATION; PERFORMANCE; OXIDATION; ACID;
D O I
10.1016/j.cclet.2017.09.025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
TiO2/EDTA-rich carbon composites (TiO2/EDTA-RC) have been successfully synthesized via a low temperature carbonization process. TiO2/EDTA-RC exhibits marked absorption of visible light and excellent photoreduction of Cr(VI) activity under visible light irradiation (lambda > 420 nm). Due to the high carboxyl group content and strong coordination ability of EDTA, TiO2-EDTA complex can be easily fabricated between EDTA incorporated in carbon sheet and titanol group on the surface of TiO2. TiO2-EDTA complexes on the surface of TiO2/EDTA-RC, the LMCT complex, are responsible for the prominent photoreduction of Cr(VI) properties of TiO2/EDTA-RC under visible light irradiation. In addition, the unique structure of TiO2/EDTA-RC is also propitious to the visible-light photocatalytic reduction of Cr(VI). Carbon sheet of TiO2/EDTA-RC acts as a supporter. TiO2 nanoparticles and EDTA homogeneously disperse into the carbon sheet supporter and form the TiO2-EDTA complexes, which can avoid the aggregation of TiO2 nanoparticles in the aqueous solution and provide more photocatalytic reaction points for the reduction of Cr(VI). (C) 2017 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:547 / 550
页数:4
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