Sonocatalytic activity of LuFeO3 crystallites synthesized via a hydrothermal route

被引:13
|
作者
Zhou, Ming [1 ]
Yang, Hua [1 ]
Xian, Tao [1 ]
Yang, Yang [1 ]
Zhang, Yunchuan [1 ]
机构
[1] Lanzhou Univ Technol, Sch Sci, Lanzhou 730050, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Lutetium orthoferrite; Hydrothermal synthesis; Sonocatalytic activity; Hydroxyl radical; Inorganic anion; Degradation of organic dyes; METHYL-ORANGE; DEGRADATION; PARTICLES; PHOTOCATALYSIS; NANOPARTICLES; PROPERTY; OXYGEN; IONS;
D O I
10.1016/S1872-2067(15)60941-X
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
LuFeO3 crystallites of different sizes and morphologies were synthesized via a hydrothermal route. The sonocatalytic properties of the as-synthesized samples were investigated by degrading various organic dyes, including acid orange 7 (AO7), rhodamine B (RhB), methyl orange (MO), and methylene blue (MB), under ultrasonic irradiation, revealing that they exhibit excellent sonocatalytic activity toward the degradation of these dyes. Particularly, the synthesized bar-like particles with lengths of similar to 3 mu m and widths of similar to 1 mu m have the highest sonocatalytic activity, and the degradation percentage of AO7 reaches 89% after 30 min of sonocatalysis. The effects of inorganic anions such as Cl-, NO3-, SO42-, PO43-, and HCO3- on the sonocatalysis efficiency were investigated. Hydroxyl radicals ((OH)-O-center dot) detected by fluorimetry using terephthalic acid as a probe molecule were found to be produced over the ultrasonic-irradiated LuFeO3 particles. The addition of ethanol, which acts as a (OH)-O-center dot scavenger, leads to quenching of (OH)-O-center dot radicals and a simultaneous decrease in the dye degradation. This suggests that (OH)-O-center dot is the dominant active species responsible for the dye degradation. (C) 2015, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1987 / 1994
页数:8
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