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零价铁-过硫酸盐体系同时去除水中酸性橙7和磷
引用本文:聂明华,吴乐良,余林兰,张艺民,张文静,徐文丽,董文博,晏彩霞. 零价铁-过硫酸盐体系同时去除水中酸性橙7和磷[J]. 环境科学学报, 2018, 38(11): 4321-4332
作者姓名:聂明华  吴乐良  余林兰  张艺民  张文静  徐文丽  董文博  晏彩霞
作者单位:江西师范大学地理与环境学院, 鄱阳湖湿地与流域研究教育部重点实验室, 南昌 330022,江西师范大学地理与环境学院, 鄱阳湖湿地与流域研究教育部重点实验室, 南昌 330022,江西师范大学地理与环境学院, 鄱阳湖湿地与流域研究教育部重点实验室, 南昌 330022,江西师范大学地理与环境学院, 鄱阳湖湿地与流域研究教育部重点实验室, 南昌 330022,江西师范大学地理与环境学院, 鄱阳湖湿地与流域研究教育部重点实验室, 南昌 330022,江西师范大学地理与环境学院, 鄱阳湖湿地与流域研究教育部重点实验室, 南昌 330022,复旦大学环境科学与工程系, 上海市大气颗粒物污染与防治重点实验室, 上海 200433,江西师范大学地理与环境学院, 鄱阳湖湿地与流域研究教育部重点实验室, 南昌 330022
基金项目:国家自然科学基金(No.41601523,41601521);江西省自然科学基金(No.20161BAB213079,20161BAB213077);鄱阳湖湿地与流域研究教育部重点实验室开放基金(No.PK2016006);江西省教育厅科技计划项目(No.GJJ150307,GJJ160320)
摘    要:采用零价铁(ZVI)活化过硫酸盐(PS)同时去除水中酸性橙7(AO7)和磷.ZVI-PS体系可以产生强氧化性的SO·-4和HO·,从而去除水中AO7.同时,ZVI最终转化为Fe3+,因此可以用来去除水中磷.结果表明,ZVI-PS体系在酸性条件下可以有效的同时去除水中AO7和磷.淬灭实验结果表明,硫酸根自由基(SO·-4)对AO7的降解起主要作用.水中共存的阴离子和腐植酸(HA)对AO7和磷的去除均有抑制作用,其对AO7和磷去除的抑制能力排序均为:HCO-3 NO-2 HA NO-3 Cl-.AO7和磷在超纯水中的去除率高于其他实际水体,但反应60 min后,实际水体中AO7和磷的去除率也分别高达80.31%~92.69%和87.54%~100%,因此,该体系对实际水体中AO7和磷的处理有潜在的应用价值.通过紫外-可见分光光谱和GC-MS分析说明,AO7经过偶氮键断键后的中间产物进一步氧化形成含苯环类物质.同时,TOC有所降低,说明部分AO7被矿化为CO2和H2O.

关 键 词:硫酸根自由基  酸性橙7    共存物质  降解产物
收稿时间:2018-04-29
修稿时间:2018-06-27

Simultaneous removal of acid orange 7 and phosphate from water using zero-valent iron activated persulfate system
NIE Minghu,WU Leliang,YU Linlan,ZHANG Yimin,ZHANG Wenjing,XU Wenli,DONG Wenbo and YAN Caixia. Simultaneous removal of acid orange 7 and phosphate from water using zero-valent iron activated persulfate system[J]. Acta Scientiae Circumstantiae, 2018, 38(11): 4321-4332
Authors:NIE Minghu  WU Leliang  YU Linlan  ZHANG Yimin  ZHANG Wenjing  XU Wenli  DONG Wenbo  YAN Caixia
Affiliation:Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, School of Geography and Environment, Jiangxi Normal University, Nanchang 330022,Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, School of Geography and Environment, Jiangxi Normal University, Nanchang 330022,Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, School of Geography and Environment, Jiangxi Normal University, Nanchang 330022,Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, School of Geography and Environment, Jiangxi Normal University, Nanchang 330022,Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, School of Geography and Environment, Jiangxi Normal University, Nanchang 330022,Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, School of Geography and Environment, Jiangxi Normal University, Nanchang 330022,Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of Environmental Science and Engineering, Fudan University, Shanghai 200433 and Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, School of Geography and Environment, Jiangxi Normal University, Nanchang 330022
Abstract:In the present study, zero-valent iron (ZVI) was used as a catalyst to activate persulfate (PS) for the simultaneous removal of acid orange 7 (AO7) and phosphate from aqueous solutions. Sulfate radicals (SO4·-) and hydroxyl radical (HO·) can be generated in ZVI-PS system which may participate in the oxidation of AO7. Meanwhile, ZVI is ultimately transformed to Fe3+, which can potentially serve as a coagulant to remove phosphate. Experimental results indicate that AO7 and phosphate could be simultaneously removed in this process. A stronger acidic condition is more favourable for AO7 and phosphate removal. Radical scavenging tests reveal that the predominant reactive oxygen species for AO7 degradation was SO4·-. Coexisting substances inhibited the AO7 and phosphate removal, and the inhibition of these substances followed the order of HCO3- > NO- 2 > humic acid (HA) > NO3- > Cl-. The removal efficiencies of AO7 and phosphate were lower in real waters than in ultrapure water. Nevertheless, up to 80.31%~92.69% and 87.54%~100% of AO7 and phosphate were removed from the real waters within 60 min, respectively. From the analysis of UV-Vis spectra and GC-MS, it is assumed that the oxidation process is initiated by the separation of azo links. The intermediates containing various oxygenated benzene and naphthalene rings further undergo ring-opening reactions, and finally mineralized to CO2 and H2O.
Keywords:sulfate radical  acid orange 7  phosphate  coexisting substances  intermediates
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