Degradation kinetics and mechanism of trace nitrobenzene by granular activated carbon enhanced microwave/hydrogen peroxide system

被引:14
作者
Tani, Dina [1 ,2 ]
Zeng, Honghu [1 ]
Liu, Jie [1 ]
Yu, Xiaozhang [1 ]
Liang, Yanpeng [1 ]
Lu, Lanjing [3 ]
机构
[1] Guilin Univ Technol, Coll Environm Sci & Engn, Guilin 541004, Peoples R China
[2] Guangxi Inst Bldg Res & Design, Nanning 530011, Peoples R China
[3] Guangxi Polytech Construct, Nanning 530003, Peoples R China
基金
中国国家自然科学基金;
关键词
microwave; granular activated carbon; hydrogen peroxide; nitrobenzene; hydroxyl radicals; AQUEOUS-SOLUTION; OXIDATION; REMOVAL; CATALYST; ADSORPTION; ENERGY; OZONE; WATER;
D O I
10.1016/S1001-0742(12)60183-1
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The kinetics of the degradation of trace nitrobenzene (NB) by a granular activated carbon (GAC) enhanced microwave (MW)/hydrogen peroxide (H2O2) system was studied. Effects of pH, NB initial concentration and tert-butyl alcohol on the removal efficiency were examined. It was found that the reaction rate fits well to first-order reaction kinetics in the MW/GAC/H2O2 process. Moreover, GAC greatly enhanced the degradation rate of NB in water. Under a given condition (MW power 300 W, H2O2 dosage 10 mg/L, pH 6.85 and temperature (60 +/- 5)degrees C), the degradation rate of NB was 0.05214 min(-1) when 4 g/L GAC was added. In general, alkaline pH was better for NB degradation; however, the optimum pH was 8.0 in the tested pH value range of 4.0-12.0. At H2O2 dosage of 10 mg/L and GAC dosage of 4 g/L, the removal of NB was decreased with increasing initial concentrations of NB, indicating that a low initial concentration was beneficial for the degradation of NB. These results indicated that the MW/GAC/H2O2 process was effective for trace NB degradation in water Gas chromatography-mass spectrometry analysis indicated that a hydroxyl radical addition reaction and dehydrogenation reaction enhanced NB degradation.
引用
收藏
页码:1492 / 1499
页数:8
相关论文
共 28 条
[1]   The role of activated carbon as a catalyst in GAC/iron oxide/H2O2 oxidation process [J].
Bach, Altai ;
Semiat, Raphael .
DESALINATION, 2011, 273 (01) :57-63
[2]   Photocatalytic degradation of nitrobenzene using titanium dioxide and concentrated solar radiation: chemical effects and scaleup [J].
Bhatkhande, DS ;
Pangarkar, VG ;
Beenackers, AACM .
WATER RESEARCH, 2003, 37 (06) :1223-1230
[3]   Preparation and characteristics of carbon-supported platinum catalyst and its application in the removal of phenolic pollutants in aqueous solution by microwave-assisted catalytic oxidation [J].
Bo, Longli ;
Quan, Xie ;
Wang, Xiaochang ;
Chen, Shuo .
JOURNAL OF HAZARDOUS MATERIALS, 2008, 157 (01) :179-186
[4]   Degradation of p-nitrophenol in aqueous solution by microwave assisted oxidation process through a granular activated carbon fixed bed [J].
Bo, Longli ;
Quan, Xie ;
Chen, Shuo ;
Zhao, Huimin ;
Zhao, Yazhi .
WATER RESEARCH, 2006, 40 (16) :3061-3068
[5]  
Chen P, 2004, GUIZHOU CHEM IND, V29, P30
[6]   Degradation of nitrobenzene at near neutral pH using Fe2+-glutamate complex as a homogeneous Fenton catalyst [J].
ElShafei, Gamal M. S. ;
Yehia, F. Z. ;
Dimitry, O. I. H. ;
Badawi, A. M. ;
Eshaq, Gh. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2010, 99 (1-2) :242-247
[7]  
Hartter DR., 1985, Toxicity of nitroaromatic compounds, P1
[8]   Adsorption of dyes onto carbonaceous materials produced from coffee grounds by microwave treatment [J].
Hirata, M ;
Kawasaki, N ;
Nakamura, T ;
Matsumoto, K ;
Kabayama, M ;
Tamura, T ;
Tanada, S .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2002, 254 (01) :17-22
[9]   Inhibiting 1,3-dinitrobenzene formation in Fenton oxidation of nitrobenzene through a controllable reductive pretreatment with zero-valent iron [J].
Jiang, Bi-Cun ;
Lu, Zhao-Yang ;
Liu, Fu-Qiang ;
Li, Ai-Min ;
Dai, Jian-Jun ;
Xu, Ling ;
Chu, Li-Mei .
CHEMICAL ENGINEERING JOURNAL, 2011, 174 (01) :258-265
[10]   Application of Microwave Energy to Treat Granular Activated Carbon Contaminated With Chlorobenzene [J].
Jou, Chih-Ju G. ;
Wu, Chung-Rung ;
Lee, Chien-Li .
ENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, 2010, 29 (03) :272-277