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用于 Orange II 的可见光光催化的磁性核壳 CuFe2O4@C3N4 杂化物。

Magnetic core-shell CuFe2O4@C3N4 hybrids for visible light photocatalysis of Orange II.

机构信息

Anhui Key Lab of Controllable Chemical Reaction & Material Chemical Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Tunxi Road 193, Hefei 230009, China; State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing University of Technology, Nanjing 210009, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui 230026, China.

Anhui Key Lab of Controllable Chemical Reaction & Material Chemical Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Tunxi Road 193, Hefei 230009, China.

出版信息

J Hazard Mater. 2015 Oct 30;297:224-33. doi: 10.1016/j.jhazmat.2015.04.046. Epub 2015 Apr 18.

Abstract

Novel CuFe2O4@C3N4 core-shell photocatalysts were fabricated through a self-assembly method and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, transmission electron microscopy and Uv-vis diffuse reflection spectroscopy. The photocatalytic performances of the CuFe2O4@C3N4 catalysts were evaluated in photo Fenton-like discoloration of Orange II dye using H2O2 as an oxidant under visible-light irradiation (λ>420 nm). It was found the CuFe2O4@C3N4 hybrid (mass ratio of CuFe2O4/g-C3N4 at 2:1) exhibits a superior activity as compared with single component of CuFe2O4 or g-C3N4 and the mixture of g-C3N4 and CuFe2O4, due to the elevation of the separation efficiency of photoinduced electron-hole pairs, resulted from the heterojunction between the interfaces of g-C3N4 and CuFe2O4. The quenching tests of different scavengers displayed that O2(•-), OH and h(+) are responsible for the Orange II decolorization. In addition, the effects of initial concentration of the dye contaminant (0.014-0.140 mM), different anions (Cl(-), SO4(2-), NO3(-), CH3COO(-) and HCO3(-)) and temperature (15-65 °C) in photoreaction were also investigated. The CuFe2O4@C3N4 sample exhibited stable performance without obvious loss of catalytic activity after five successive runs, showing a promising application for the photo-oxidative degradation of environmental contaminants.

摘要

新型 CuFe2O4@C3N4 核壳光催化剂通过自组装法制备,并通过 X 射线衍射、傅里叶变换红外光谱、热重分析、X 射线光电子能谱、透射电子显微镜和紫外-可见漫反射光谱进行了表征。以 H2O2 为氧化剂,在可见光照射下(λ>420nm),评价了 CuFe2O4@C3N4 催化剂对橙 II 染料的光芬顿类似褪色的光催化性能。结果发现,与单一组分的 CuFe2O4 或 g-C3N4 以及 g-C3N4 和 CuFe2O4 的混合物相比,CuFe2O4@C3N4 杂化体(CuFe2O4/g-C3N4 的质量比为 2:1)具有更高的活性,这是由于 g-C3N4 和 CuFe2O4 界面之间的异质结提高了光生电子-空穴对的分离效率。不同猝灭剂的猝灭试验表明,O2(•-)、OH 和 h(+)是橙 II 脱色的原因。此外,还研究了染料污染物初始浓度(0.014-0.140mM)、不同阴离子(Cl(-)、SO4(2-)、NO3(-)、CH3COO(-)和 HCO3(-))和温度(15-65°C)对光反应的影响。CuFe2O4@C3N4 样品在五次连续运行后表现出稳定的性能,没有明显的催化活性损失,显示出在环境污染物的光氧化降解方面有很好的应用前景。

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