Electrochemical activation of sulfate by BDD anode in basic medium for efficient removal of organic pollutants

被引:117
作者
Chen, Luchuan [1 ]
Lei, Chaojun [1 ]
Li, Zhongjian [1 ]
Yang, Bin [1 ]
Zhang, Xingwang [1 ]
Lei, Lecheng [1 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Minist Educ, Key Lab Biomass Chem Engn, Hangzhou 310027, Zhejiang, Peoples R China
关键词
Electrochemical advanced oxidation processes; Boron doped diamond anode; Sulfate radicals; Basic mediums; BORON-DOPED DIAMOND; ADVANCED OXIDATION PROCESSES; WASTE-WATER TREATMENT; HYDROXYL RADICALS; PH CONDITIONS; DEGRADATION; NANOPARTICLES; PERSULFATES; GENERATION; PRETREATMENT;
D O I
10.1016/j.chemosphere.2018.07.043
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electrochemical advanced oxidation processes (EAOPs) based on hydroxyl radicals ((OH)-O-center dot) have some limitations when they are applied to real wastewater treatment, such like strict requirements on pH (acidic electrolyte) and high energy consumption. Compared to (OH)-O-center dot, Sulfate radicals (SO4 center dot-) have high redox potential in wider range of pH (2-9). In this study, SO4 center dot(-) were efficiently produced by electrochemical activation of SO42- at boron doped diamond (BDD) anode. The degradation rate of 2,4-DCP (k = 0.828 +/- 0.05 h(-1)) in the presence of Na2SO4 was approximately 4 times than that without Na2SO4 (k = 0.219 +/- 0.01 h(-1)), indicating that SO4 center dot- exhibited higher reactivity than (OH)-O-center dot at initial pH = 9. Moreover, the amount of O-2 decreased by 65% after 100 min during electro-oxidation of 2,4-DCP and the specific energy consumption per unit TOC (ECTOC) was reduced by 70% when the concentration of Na2SO4 increased from 0.01 to 0.1 M. The impact of sulfate ions in the electrochemical advanced oxidation were investigated. Electron spin resonance (ESR) measurements were conducted to identify the formation of SO4 center dot-. Electrolysis of 2,4-DCP with specific radical scavengers (ethanol and tert-Butanol) were conducted and the results revealed that SO4 center dot- were mainly produced by one-electron loss of sulfate at basic condition. Electro-generation persulfate was measured and participation of non-radical activation of per sulfate was investigated. O-2 production was quantified and we found electrochemical activation of sulfate could inhibit water dissociation. Taken all findings, a mechanism of electrochemical activation of sulfate at BDD anode was summarized. This technology eliminates the requirement for pH adjustment for wastewater treatment and makes EAOPs more effective and economic as well. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:516 / 523
页数:8
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