首页 | 本学科首页   官方微博 | 高级检索  
     检索      

NC-PC锚定微量Fe活化PMS降解水中2,4-二氯苯氧乙酸
引用本文:郭枭杰,方志勇,周鑫,罗豪鹏,周娟.NC-PC锚定微量Fe活化PMS降解水中2,4-二氯苯氧乙酸[J].中国环境科学,2021,41(7):3238-3246.
作者姓名:郭枭杰  方志勇  周鑫  罗豪鹏  周娟
作者单位:东华大学环境工程系, 上海 201620
基金项目:国家重点研发计划课题资助(2019YFC0408505)
摘    要:采用分步热分解法制备了NC-PC(三维多孔碳材料)锚定的微量Fe基催化剂,用于活化过一硫酸盐(PMS)氧化降解水中2,4-二氯苯氧乙酸(2,4-D).采用透射电子显微镜(TEM)、高精度比表面积仪(BET)、X射线光电子能谱分析(XPS)和电感耦合等离子体发射光谱分析(ICP)对催化剂进行表征.考察了不同金属、制备方法、催化剂投加量、PMS投加量、初始pH值以及水中不同阴离子(Cl-、NO3-、HCO3-)对2,4-D降解的影响.结果表明,通过热分解法合成的Fe-NC-PC对2,4-D具有更好的降解效果,当2,4-D初始浓度为0.1mmol/L,初始pH=3.4,催化剂投加量0.15g/L,PMS浓度0.7mmol/L时,反应20min内2,4-D的去除率可达91%.随着催化剂投加量、PMS投加量的提高,2,4-D的降解效果提高;随着初始pH值的提高,2,4-D的降解效率逐渐降低;水中不同阴离子(Cl-、NO3-、HCO3-)和腐殖酸(HA)对2,4-D的降解有轻微的抑制作用.通过自由基淬灭实验、EPR测试以及XPS分析了反应的主要活性物种和反应机理,发现材料制备过程中形成的Fe-Nx是主要的反应活性位,能够有效的活化PMS降解水中2,4-D,1O2在2,4-D的降解过程中起到主要作用.

关 键 词:氮掺杂碳负载微量铁催化剂  过一硫酸盐  2  4-二氯苯氧乙酸  单线态氧  
收稿时间:2020-12-03

NC-PC anchors trace Fe to activate PMS to degrade 2,4-dichlorophenoxyacetic acid in water
GUO Xiao-Jie,FANG Zhi-Yong,ZHOU Xin,LUO Hao-Peng,ZHOU Juan.NC-PC anchors trace Fe to activate PMS to degrade 2,4-dichlorophenoxyacetic acid in water[J].China Environmental Science,2021,41(7):3238-3246.
Authors:GUO Xiao-Jie  FANG Zhi-Yong  ZHOU Xin  LUO Hao-Peng  ZHOU Juan
Institution:College of Environmental Science and Engineering, Donghua University, Shanghai 201620, China
Abstract:A small amount of Fe-based catalyst anchored by NC-PC (three-dimensional porous carbon material) was prepared by a step-by-step thermal decomposition method, which was used to activate permonosulfate (PMS) to oxidize and degrade 2,4-dichlorophenoxyacetic acid (2,4-D) in water. The catalysts were characterized by transmission electron microscopy (TEM), fully automatic rapid surface measurement (BET), X-ray photoelectron spectroscopy (XPS) and inductively coupled plasma emission spectroscopy (ICP). The effects of different metals, preparation methods, catalyst dosage, PMS dosage, initial pH, and different anions (Cl-, NO3-, HCO3-) on the degradation of 2,4-D were investigated. Fe-NC-PC synthesized by thermal decomposition method has a better degradation effect on 2,4-D, when the initial concentration of 2,4-D was 0.1mmol/L, the initial pH=3.4, the catalyst was added When the amount was 0.15g/L and the PMS concentration was 0.7mmol/L, the 2,4-D removal rate can reach 91% within 20 minutes of reaction.With the increase of the dosage of catalyst and PMS, the degradation effect of 2,4-D increased; with the increase of initial pH, the degradation efficiency of 2,4-D gradually decreased; different anions in water (Cl-, NO3-, HCO3-) and humic acid (HA) has a slight inhibitory effect on the degradation of 2,4-D.Through radical quenching experiment, EPR test and XPS analysis of the main active species and reaction mechanism of the reaction, it was found that Fe-Nx formed during the material preparation process was the main reactive site, which can effectively activate PMS to degrade 2,4-D in water, 1O2 plays an important role in the degradation of 2,4-D.
Keywords:Fe-NC-PC  peroxymonosulfate  2  4-dichlorophenoxyacetic acid  1O2  
本文献已被 CNKI 等数据库收录!
点击此处可从《中国环境科学》浏览原始摘要信息
点击此处可从《中国环境科学》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号