Catalytic oxidation of 4-chlorophenol on in-situ sulfur-doped activated carbon with sulfate radicals

被引:71
作者
Guo, Yaoping [1 ,2 ]
Zeng, Zequan [1 ]
Li, Yulin [1 ,2 ]
Huang, Zhanggen [1 ]
Yang, Jieyang [1 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulfur doping; Activated carbon; Persulfate oxidation; 4-chlorophenol degradation; Advanced oxidation process; OXYGEN REDUCTION REACTION; MAGNETIC NANO-PARTICLES; ZERO-VALENT IRON; PERSULFATE OXIDATION; ORGANIC CONTAMINANTS; PHENOL ADSORPTION; MESOPOROUS CARBON; REACTIVE RADICALS; DEGRADATION; REMOVAL;
D O I
10.1016/j.seppur.2017.02.006
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In-situ S-doped activated carbon (ACS) was prepared and used as a heterogeneous catalyst to activate persulfate (PS) for 4-chlorophenol (4CP) oxidation. The effects of several operation parameters, including PS concentration, initial pH, ACS dosage, and reaction temperature, on 4CP degradation were investigated in detail via batch experiments. Results show that ACS exhibited excellent catalytic activity for PS activation and a complete 4CP degradation as well as 653% COD removal can be achieved in 170 min at 25 degrees C with ACS dosage of 0.1 g/L, PS/4CP molar ratio of 24/1 and initial pH of 4.4. The biodegradability was greatly improved after a 170 min reaction. Quenching tests reveal that SO4-. was the dominant active species taking part in the degradation of 4CP. Based on the stability tests and the corresponding characterizations of ACS before and after use, it was speculated that the loss of the specific surface area and the change of the surface chemistry led to the significant deactivation of ACS. Meanwhile, a possible mechanism of PS activation on ACS was proposed. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 264
页数:8
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