Catalytic wet air oxidation of phenols over porous plate Cu-based catalysts

被引:27
|
作者
Lai, Chujun [1 ]
He, Tianqu [1 ]
Li, Xuewen [1 ]
Chen, Fang [2 ]
Yue, Linhai [2 ]
Hou, Zhaoyin [1 ,3 ]
机构
[1] Zhejiang Univ, Dept Chem, Key Lab Biomass Chem Engn, Minist Educ, Hangzhou 310028, Peoples R China
[2] Zhejiang Univ, Dept Chem, Hangzhou 310028, Peoples R China
[3] Zhejiang Univ, Ctr Chem Frontier Technol, Dept Chem, Hangzhou 310028, Peoples R China
基金
中国国家自然科学基金;
关键词
Phenol; Degradation; Catalytic wet air oxidation; Cu catalyst; LAYERED DOUBLE HYDROXIDE; WASTE-WATER; PHOTOELECTROCATALYTIC DEGRADATION; PEROXIDE OXIDATION; PERFORMANCE; DYE; ELECTROCATALYST; ULTRASOUND; GENERATION; HYDROGEN;
D O I
10.1016/j.clay.2019.105253
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
Catalytic wet air oxidation (CWAO) of phenol has attracted much attention because of its high versatility and remarkable economy-scale advantages. In this submission, a series of M-3-Al-500 catalysts (with M = Cu, Mn, Fe, Ni, Zn and Co) were prepared via controlled calcination of layered double hydroxides, and tested in the CWAO of high concentrated phenol (2.1 g/L) with air under mild condition (120 degrees C and 1.0 MPa). It was found that Cu-3-Al-500 was the most active among these tested catalysts as phenol converted completely within 2 h. Characterizations indicated that the performance of Cu-based catalyst could be attributed to the redox transitions of Cu2+/Cu+ and/or the formation of H2O2 in reaction mixture. At the same time, the surface acidity of Cu-3-Al-500 can also accelerate the degradation of phenol. The possible degradation mechanism of phenol over Cu-based catalyst was proposed.
引用
收藏
页数:7
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