Improved degradation of anthraquinone dye by electrochemical activation of PDS

被引:75
|
作者
Li, Xue [1 ]
Tang, Shoufeng [1 ]
Yuan, Deling [1 ]
Tang, Jiachen [1 ]
Zhang, Chen [1 ]
Li, Na [1 ]
Rao, Yandi [1 ]
机构
[1] Yanshan Univ, Sch Environm & Chem Engn, Hebei Key Lab Appl Chem, Qinhuangdao 066004, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical oxidation; Peroxydisulfate activation; Anthraquinone dye removal; Inorganic anions; WASTE-WATER; RADICAL REACTIONS; AQUEOUS-SOLUTION; ELECTRIC-FIELD; SELF-DRIVEN; PERSULFATE; REMOVAL; CARBON; OXIDATION; PEROXYMONOSULFATE;
D O I
10.1016/j.ecoenv.2019.04.015
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electrochemical oxidation (EO) coupled with peroxydisulfate (PDS) activation as a synergistic wastewater treatment process (PDS/EO) was performed to degrade anthraquinone dye-Reactive Brilliant Blue (RBB) in aqueous solution. Introducing PDS into the EO improved the RBB removal than the sole PDS and conventional EO systems. The RBB could activate PDS to a certain degree by itself. By the comparison of various inorganic ions addition, it showed that adding NO3- as the background electrolyte was more effective than the systems using the Cl- and SO42-, respectively. In this PDS/EO-NO3- system, increasing PDS concentration (1-5 mmol L-1) and current density (5-10 mA cm(-2)) considerably promoted the degradation of RBB. The adjustment of the solution pH displayed that the acidic and neutral condition was beneficial to the RBB removal, and the synergistic effect was inverse ratio to the RBB initial concentration. Furthermore, the scavenger experiments verified that both SO4 center dot- and HO center dot were the major active substances in the RBB decomposition, and other reactive oxygen species also had considerable contributions. Thereinto NO3- only act a catalytic agent to improve the generation of active matters in the PDS/EO-NO3-. Overall, the proposed synergistic process could serve as an efficient method for the degradation of anthraquinone dye.
引用
收藏
页码:77 / 85
页数:9
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