Degradation of Phenol Using Peroxymonosulfate Activated by a High Efficiency and Stable CoMgAl-LDH Catalyst

被引:16
作者
Liao, Zhuwei [1 ]
Zhu, Jingyi [1 ]
Jawad, Ali [1 ]
Muzi, Jiajing [2 ]
Chen, Zhuqi [3 ]
Chen, Zhulei [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Environm Sci & Engn, Wuhan 430074, Hubei, Peoples R China
[2] GAD Environm Co Ltd, Shenzhen 518067, Peoples R China
[3] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Hubei Key Lab Mat Mat & Serv Failure, Minist Educ,Sch Chem & Chem Engn, Wuhan 430074, Hubei, Peoples R China
基金
国家重点研发计划;
关键词
advanced oxidation processes; layered double hydrotalcite; hydrothermal method; reusability; ADVANCED OXIDATION PROCESSES; LAYERED DOUBLE HYDROXIDES; RADICAL GENERATION; SULFATE; WATER; KINETICS;
D O I
10.3390/ma12060968
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
In this study, we report on an active and stable CoMgAl layered double hydrotalcite (LDH) catalyst for phenol degradation by heterogeneous activation of peroxymonosulfate (PMS). The CoMgAl-LDH catalyst was synthesized by hydrothermal method. The PMS/CoMgAl-LDH system overcomes the drawbacks of traditional Fenton processes. Various effects, e.g., scavengers, chloride ion, catalyst dosage, PMS concentration, temperature, and pH, were also inspected to evaluate the system. The results indicated that the PMS/CoMgAl-LDH system had extremely high efficiency for phenol degradation; 0.1 mM phenol could be completely degraded by 0.3 g/L catalyst and 3 mM PMS within 60 min at 30 degrees C. The CoMgAl-LDH catalyst appeared to possess outstanding reusability and stability. After four rounds of recycling, nearly 100% of the phenol was removed within 80 min by the PMS/CoMgAl-LDH system, with only 0.05 mg/L Co2+ leaching. A sulfate radical was the main oxidation species in the PMS/Co-LDH system. The degradation rate of phenol was influenced by temperature, and the activation energy was 65.19 kJ/mol. These advantages proved the PMS/CoMgAl-LDH system is an effective strategy for the treatment of organic contaminants.
引用
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页数:13
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