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高盐强酸性地下水中复合苯系污染物原位芬顿氧化实验研究
引用本文:郭威,袁放,张佳,谢斌,冯学洋,陈鸿汉.高盐强酸性地下水中复合苯系污染物原位芬顿氧化实验研究[J].水文地质工程地质,2021,48(2):182-189.
作者姓名:郭威  袁放  张佳  谢斌  冯学洋  陈鸿汉
作者单位:1.中国地质大学(北京)水资源与环境学院北京市重点实验室,北京 100083
基金项目:国家重点研发计划项目资助(2018YFC1800400)。
摘    要:在原位氧化过程中,实际场地地下水和含水介质的物化特征是影响氧化效果的重要因素,而目前对此影响的研究较少。以某场地实际高盐强酸性复合苯系污染地下水为研究对象,以地下水中2-硝基-4-甲氧基苯胺(2-nitro-4-methoxyaniline,2-N)和3-硝基-4-甲氧基苯胺(3-nitro-4-methoxyaniline,3-N)为特征污染物,探究芬顿(Fenton)试剂原位氧化特征,并研究液相环境因素(初始H2O2浓度、初始Fe2+浓度、初始pH值、初始醋酸(Acetic acid,HAc)浓度、初始SO42-浓度)以及含水层介质对Fenton法去除2-N和3-N的影响。结果显示:(1)Fenton法去除2-N和3-N效果显著,且在初始液相条件为c(H2O2)=7 mmol/L、c(Fe2+)=4 mmol/L、pH=4、c(HAc)=0 mg/L和c(SO42-)=0 mmol/L时去除效果最佳;(2)各因素对Fenton法氧化2-N和3-N的影响不同,加入H2O2和Fe2+使2-N和3-N去除率上升,增大HAc浓度使2-N和3-N去除率下降;(3)含水层介质对2-N和3-N具有一定吸附性,且对3-N的吸附性强于2-N,二者在本实验中最大吸附态占比分别为29%和42%,而吸附态的存在会抑制Fenton法对2-N和3-N的去除;(4)矿物分析结果显示介质含有少量黄铁矿,在硫酸环境下,介质腐蚀溶解释放Fe2+,在达到一定浓度后,无需额外添加Fe2+即可完成Fenton反应进而去除2-N和3-N。

关 键 词:芬顿    原位氧化    2-硝基-4-甲氧基苯胺    3-硝基-4-甲氧基苯胺    地下水污染    含水层介质
收稿时间:2020-12-11

In-situ Fenton oxidation experiment of compound benzene pollutants in high salt and strong acid groundwater
GUO Wei,YUAN Fang,ZHANG Jia,XIE Bin,FENG Xueyang,CHEN Honghan.In-situ Fenton oxidation experiment of compound benzene pollutants in high salt and strong acid groundwater[J].Hydrogeology and Engineering Geology,2021,48(2):182-189.
Authors:GUO Wei  YUAN Fang  ZHANG Jia  XIE Bin  FENG Xueyang  CHEN Honghan
Institution:1.Beijing Key Laboratory of School of Water Resources and Environment, China University of Geosciences (Beijing), Beijing 100083, China2.Ecological Environment Monitoring Station, Zhongwei, Ningxia 755000, China
Abstract:In the process of in-situ oxidation,the physical and chemical characteristics of actual ground water and water-bearing media are the important factors affecting the oxidation effect,but there are few specific studies on this effect at present.The actual high-salt and strong-acid compound benzene contaminated groundwater in a certain site is used as the research object,and 2-nitro-4-methoxyaniline(2-N)and 3-nitro-4-methoxyaniline(3-N)in groundwater are characteristic pollutants.The in-situ oxidation characteristics of Fenton’s reagent are explored,and the liquid environmental factors(initial H2O2 concentration,initial Fe2+concentration,initial pH value,initial acetic acid(HAc)concentration,initial SO42-concentration)and aquifer media on the removal of 2-N and 3-N by Fenton method are examined.The results show that(1)the Fenton method has a significant effect on removal of 2-N and 3-N,and when the initial liquid phase conditions are c(H2O2)=7 mmol/L,c(Fe2+)=4 mmol/L,pH=4,c(HAc)=0 mg/L and c(SO42-)=0 mmol/L,the removal effect is the best.(2)Each factor affects the oxidation of 2-N and 3-N by the Fenton method.The effect of the addition of H2O2 and Fe2+increases the removal rate of 2-N and 3-N.Increase in the concentration of HAc decreases the removal rate of 2-N and 3-N.(3)The groundwater medium has a strong effect on 2-N and 3-N,and the adsorption of 3-N is stronger than that of 2-N.In this experiment,the two largest adsorption states accounte for 29%and 42%,respectively.The existence of the adsorption state will inhibit the Fenton method to 2-N.(4)The mineral analysis results show that the medium contains a small amount of pyrite.In a sulfuric acid environment,the medium corrodes and dissolves to release Fe2+.Therefore,the Fenton reaction can be completed without additional Fe2+to remove 2-N and 3-N.
Keywords:Fenton  in situ oxidation  2-nitro-4-methoxyaniline  3-nitro-4-methoxyaniline  groundwater pollution  aqueous medium
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