Effective degradation of carbamazepine using a novel electro-peroxone process involving simultaneous electrochemical generation of ozone and hydrogen peroxide

被引:32
作者
Yang, Bo [1 ,5 ]
Deng, Jianping [1 ]
Yu, Gang [2 ]
Deng, Shubo [2 ]
Li, Juying [1 ,5 ]
Zhu, Caizhen [1 ]
Zhuo, Qiongfang [3 ]
Duan, Huabo [4 ]
Guo, Tao [1 ,5 ]
机构
[1] Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen 518060, Peoples R China
[2] Tsinghua Univ, Sch Environm, POPs Res Ctr, Beijing 100084, Peoples R China
[3] South China Inst Environm Sci, Minist Environm Protect, Guangzhou 510655, Guangdong, Peoples R China
[4] Shenzhen Univ, Coll Civil Engn, Smart City Res Inst, Shenzhen 518060, Peoples R China
[5] Shenzhen Key Lab Environm Chem & Ecol Remediat, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
Electro-peroxone; Ozone; Hydrogen peroxide; Refractory pharmaceutical pollutant; DOPED TI/SNO2 ELECTRODE; WASTE-WATER TREATMENT; CELL; OZONATION; DESIGN; ACID; BLUE;
D O I
10.1016/j.elecom.2017.11.003
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
An advanced electrochemical oxidation process (electro-peroxone) involving a dual electrode system was developed to degrade recalcitrant carbamazepine (CBZ). During this electro-peroxone (E-peroxone) process, ozone was electrochemically produced by anodic oxidation of water in a membrane electrode assembly (MEA) cell and H2O2 was simultaneously generated by the sparged O-2 using a carbon-polytetrafluorethylene (C-PTFE) cathode. The O-3 and H2O2 electrogenerated in situ synergistically produce hydroxyl radicals (center dot OH), which are much more easily oxidized than O-3. As a result, the removal efficiencies of CBZ and its TOC reached 99.8% and 97.6% after 15 min and 90 min of E-peroxone treatment, respectively, these figures remaining stable after multiple tests. The E-peroxone process is therefore a promising and effective method for degrading ozone-refractory organic contaminants in wastewater.
引用
收藏
页码:26 / 29
页数:4
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