首页  |  本刊简介  |  编委会  |  投稿须知  |  订阅与联系  |  微信  |  出版道德声明  |  Ei收录本刊数据  |  封面
UV强化草酸络合Fe3+活化过硫酸盐氧化降解苯胺
摘要点击 1979  全文点击 727  投稿时间:2018-01-22  修订日期:2018-03-16
查看HTML全文 查看全文  查看/发表评论  下载PDF阅读器
中文关键词  紫外光  草酸络合铁离子  过硫酸盐  活化  氧化
英文关键词  ultraviolet light  ferric oxalate  persulfate  activation  oxidation
作者单位E-mail
韩东晖 环境保护部华南环境科学研究所, 广东省水与大气污染防治重点实验室, 广州 510655 handonghui@scies.org 
李瑛 中国科学院广州地球化学研究所, 广州 510640  
李开明 环境保护部华南环境科学研究所, 广东省水与大气污染防治重点实验室, 广州 510655  
应光国 华南师范大学环境研究院, 广州 510006  
中文摘要
      采用UV-草酸络合Fe3+[UV-Fe(C2O433-]活化过硫酸钠(PS)氧化降解苯胺,研究了Fe(C2O433-浓度,PS浓度,pH对PS活化效率及苯胺氧化降解效果的影响机制.结果表明,Fe(C2O433-浓度和pH决定了UV-Fe(C2O433-体系中Fe3+向Fe2+的转化过程,并对活化PS氧化降解苯胺产生显著影响.随着Fe(C2O433-浓度增加,PS的分解率不断提高,但当浓度高于0.75 mmol·L-1时,草酸根离子(C2O42-)对硫酸根自由基(SO4·-)的竞争以及SO4·-之间的相互淬灭作用降低了苯胺的降解效果,降解速率大小顺序为5 mmol·L-1 < 0.25 mmol·L-1 < 0.5 mmol·L-1 < 1 mmol·L-1 < 0.75 mmol·L-1;中性和碱性条件不利于Fe(C2O433-发生光化学反应生成Fe2+,但当初始pH为7和9时,由于PS活化分解过程降低反应体系pH,反应300 min时PS的活化率可分别达到74%和67%,苯胺去除率分别高达91%和97%,均高于初始pH为酸性条件下的结果;苯胺降解率随初始PS浓度增加而增大,当PS浓度大于10 mmol·L-1时,苯胺降解过程由二级反应变为准一级反应,但此时过量的PS因与SO4·-发生反应而显著降低PS用于氧化降解苯胺的利用率.
英文摘要
      Oxidative degradation of aniline by Sodium Persulfate (PS) activated with UV-ferric oxalate[UV-Fe(C2O4)33-] was studied. The effects of Fe(C2O4)33- concentration, PS concentration, and pH on PS activation and aniline degradation were investigated. Results showed that Fe(C2O4)33- concentration and pH determined the reduction process of Fe3+ into Fe2+, which had significant effects on the oxidative degradation of aniline by PS. With an increase in Fe(C2O4)33- concentration, PS decomposition increased; however, when concentrations were>0.75 mmol·L-1, aniline degradation efficiency decreased due to competition with oxalate ions (C2O42-) for SO4·-. Aniline degradation efficiency in processes with different initial Fe(C2O4)33- concentrations followed the sequence:5 mmol·L-1 < 0.25 mmol·L-1 < 0.5 mmol·L-1 < 1 mmol·L-1 < 0.75 mmol·L-1. Neutral and alkaline conditions were not conducive to Fe2+ formation via photochemical reaction. However, with initial pH values of 7 and 9, PS activation efficiency reached 74% and 67% respectively after 300 min due to pH decline during the reaction; aniline removal efficiency was as high as 91% and 97%, respectively, higher than under initial acidic conditions. Furthermore, increased PS concentration was conducive to improvement of aniline degradation efficiency, but when PS concentration was>10 mmol·L-1, the aniline degradation process followed the pseudo first-order reaction kinetics model instead of the second-order reaction kinetics model. PS efficiency for aniline degradation decreased significantly due to the reaction between excessive PS and sulfate radicals.

您是第53342497位访客
主办单位:中国科学院生态环境研究中心 单位地址:北京市海淀区双清路18号
电话:010-62941102 邮编:100085 E-mail: hjkx@rcees.ac.cn
本系统由北京勤云科技发展有限公司设计  京ICP备05002858号-2