One-pot electro-synthesis of ZrO2-ZnO/HY nanocomposite for photocatalytic decolorization of various dye-contaminants

被引:71
作者
Sapawe, N. [1 ]
Jalil, A. A. [1 ]
Triwahyono, S. [2 ]
机构
[1] Univ Teknol Malaysia, Fac Chem Engn, Inst Hydrogen Econ, Johor Baharu 81310, Johor, Malaysia
[2] Univ Teknol Malaysia, Fac Sci, Ibnu Sina Inst Fundamental Sci Studies, Johor Baharu 81310, Johor, Malaysia
关键词
EGZrO(2)-EGZnO/HY; Electrochemical; HY zeolite; Photodecolorization; Methylene blue; Dyes; METHYLENE-BLUE; ZNO NANOPARTICLES; AQUEOUS-SOLUTION; FACILE SYNTHESIS; WATER OXIDATION; CUO/X ZEOLITE; DOPED TIO2; ORANGE-G; DEGRADATION; PHOTODECOLORIZATION;
D O I
10.1016/j.cej.2013.03.121
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A highly photoreactive electrogenerated catalyst (EGZrO(2)-EGZnO/HY) was prepared by a facile one-pot electrochemical method. The restructuring of the aluminosilicate protonated Y zeolite (HY zeolite) framework presumably occurred during electrolysis via dealumination accompanied by the insertion of Zr and Zn ions resulting from anodic dissolution to form a new active species, Si coordinated with Zr and Zn in the HY framework. The photoactivity of the photocatalyst was examined by photodecolorization of methylene blue (MB) under varying pH, catalyst dosage, and initial concentrations of MB. An amount of 0.60 g L-1 1 wt.% EGZrO(2)-1 wt.% EGZnO/HY was found to be the optimum dosage for 10 mg L-1 MB, which gave almost complete photodecolorization of methylene blue after 1 h under visible light at pH 11 and room temperature. The photocatalytic reaction followed pseudo first-order kinetics which were rationalized in terms of the Langmuir-Hinshelwood model, and provided nearly complete mineralization. After five cycling runs, the catalyst was still stable and showed no leaching effect. High decolorization percentage (>80%) of other dyes such as malachite green (MG), Congo red (CR), and methyl orange (MO) were also obtained. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:254 / 265
页数:12
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