Iron-loaded carbon nanotube-microfibrous composite for catalytic wet peroxide oxidation of m-cresol in a fixed bed reactor

被引:17
作者
Yang, Yi [1 ]
Zhang, Huiping [1 ]
Huang, Haoxin [1 ]
Yan, Ying [1 ]
Zhang, Xinya [1 ]
机构
[1] South China Univ Technol, Guangdong Prov Key Lab Green Chem Prod Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon nanotube; Microfibrous composite; Catalytic wet peroxide oxidation; m-Cresol; Mechanism; CHEMICAL-VAPOR-DEPOSITION; ACTIVATED CARBON; WASTE-WATER; FE-ZSM-5; CATALYST; PHENOL; DEGRADATION; OXIDE; ACIDITY; SURFACE; FE;
D O I
10.1007/s11356-019-07362-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A kind of novel iron-loaded carbon nanotube-microfibrous composite (Fe2O3-CNT-MF) catalyst is prepared and tested for fixed bed m-cresol catalytic wet peroxide oxidation (CWPO) reaction. Results show that the Fe2O3-CNT-MF can significantly decline the pressure drop of the fixed bed. Higher temperature, lower feed flow rate, higher catalyst bed height, and higher H2O2 dosage are beneficial to m-cresol degradation. Lower pH can also improve m-cresol degradation, but it will cause severe iron leaching. The highest m-cresol removal (over 99.5%) and total organic carbon (TOC) removal (53.6%) can be observed under condition of 2 cm bed height, flow rate of 2 mL/min, reaction temperature of 70 degrees C, 6 g/L H2O2, and initial pH = 1. Meanwhile, the Fe2O3-CNT-MF catalyst shows good stability with less than 10% decrease in m-cresol conversion and 7% decrease in TOC conversion after 24-h reaction and less than 2 mg/L iron leaching is observed in all conditions except for strong acid condition. Two probable pathways of m-cresol degradation process are presented. Under most conditions, m-cresol will first be turned into methylhydroquinone, followed by oxidation to p-toluquinone. In basic condition, some m-cresol will first be changed into 4-methylpyrocatechol. These aromatic intermediates will then be oxidized into some small molecular acids and finally be mineralized to CO2 and H2O.
引用
收藏
页码:6338 / 6351
页数:14
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