Enhanced removal of organic contaminants in water by the combination of peroxymonosulfate and carbonate

被引:93
|
作者
Nie, Minghua [1 ]
Zhang, Wenjing [1 ]
Yan, Caixia [1 ]
Xu, Wenli [1 ]
Wu, Leliang [1 ]
Ye, Yuping [1 ]
Hu, Yun [1 ]
Dong, Wenbo [2 ]
机构
[1] Jiangxi Normal Univ, Minist Educ, Sch Geog & Environm, Key Lab Poyang Lake Wetland & Watershed Res, Nanchang 330022, Jiangxi, Peoples R China
[2] Fudan Univ, Dept Environm Sci & Engn, Shanghai Key Lab Atmospher Particle Pollut & Prev, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Peroxymonosulfate; Carbonate; Organic pollutants; Advanced oxidation process; Water matrices; ACID ORANGE 7; THERMALLY ACTIVATED PERSULFATE; ADVANCED OXIDATION PROCESS; AQUEOUS-SOLUTION; WASTE-WATER; EFFICIENT DEGRADATION; HYDROGEN-PEROXIDE; SINGLET OXYGEN; RATE CONSTANTS; SOLAR LIGHT;
D O I
10.1016/j.scitotenv.2018.08.065
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, a favorable CO32-/PMS system for efficient degradation of organic contaminants (acid orange 7 (AO7), acetaminophen, para-aminobenzoic acid, phenol, methylene orange, methylene blue) inwater was firstly reported. Under optimal conditions, the decolorization ration of AO7 was 100% within 40 min. Data fitting showed that the AO7 decolorization could be described by the pseudo-first-order kinetics, and the rates constant values ranging from 0.0006 to 0.2297 min(-1) depending on the operating parameters (initial PMS, CO32-, AO7 concentrations). Radical scavenging studies revealed that superoxide anion radical (O-2 center dot(-)) and singlet oxygen (O-1(2)) rather than sulfate (SO4 center dot(-)) nor hydroxyl (HO center dot) were the dominant oxidants might be responsible for AO7 degradation. The presence of NO3-, HPO42-and lowconcentration of Cl-, NO2-, HCO3-, H2PO4-, HA had no significantly effect on the decolorization of AO7. Adding a higher Cl-concentration displayed favorable effects on the removal efficiencies of AO7, but adding a higher NO2-, HCO3-, H2PO4- and HA concentration apparently inhibited this process. The decolorization of AO7 was lower in wastewater in comparison to other natural waters and ultrapure water, which was probably due to the presence of higher concentration of colloids in wastewater. Nevertheless, up to 94.8%, 97.0% and 85.1% of AO7 were degraded from the filtrate, permeate, and retentate phases of wastewater within 60 min, respectively. Consequently, CO32-/PMS would be promising for removal methodology for AO7 in wastewater containing considerable colloids. Finally, three intermediates were identified and degradation pathways of AO7 were proposed. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:734 / 743
页数:10
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