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紫外激活过硫酸盐降解莠灭净的动力学研究
引用本文:李卫平,王超慧,于玲红,高乃云,杨文焕.紫外激活过硫酸盐降解莠灭净的动力学研究[J].中国环境科学,2016,36(11):3341-3347.
作者姓名:李卫平  王超慧  于玲红  高乃云  杨文焕
作者单位:1. 内蒙古科技大学能源与环境学院, 内蒙古 包头 014010; 2. 同济大学污染控制与资源化研究国家重点实验室, 上海 200092
基金项目:国家科技重大项目(2012ZX07403-001)
摘    要:采用紫外(UV)激活过硫酸盐(PS)氧化降解水中莠灭净(AMT).比较了单独UV和UV/PS两种工艺的降解效果和经济性,并考察了底物初始浓度、PS投加量以及反应初始pH值3个因素对UV/PS去除AMT动力学的影响.同时采用间接法对反应中生成的主要自由基进行了鉴定.结果表明:UV/PS比单独UV系统降解AMT更经济有效.AMT降解过程符合准一级动力学模型(R2≥0.95),随着底物浓度的增加,准一级反应速率常数kobs逐渐减小;kobs随PS投加量的增加逐渐增大;控制pH为5~10时,kobs逐渐减小,pH值为5时,kobs达到最大值,为0.0540min-1;pH为7时反应中主要生成的自由基为·SO4-.

关 键 词:过硫酸盐  莠灭净  影响因素  动力学  
收稿时间:2016-03-10

Kinetic study of ametryn degradation by UV activated persulfate
LI Wei-ping,WANG Chao-hui,YU Ling-hong,GAO Nai-yun,YANG Wen-huan.Kinetic study of ametryn degradation by UV activated persulfate[J].China Environmental Science,2016,36(11):3341-3347.
Authors:LI Wei-ping  WANG Chao-hui  YU Ling-hong  GAO Nai-yun  YANG Wen-huan
Institution:1. School of Energy and Environment, Inner Mongolia University of Science and Technology, Baotou 014010, China; 2. State Key Laboratory of Pollution Control & Resources Reuse, Tongji University, Shanghai 200092, China
Abstract:The degradation of the ametryn (AMT) by means of UV/Persulfate (PS) was investigated.The effect of degradation and economical efficiency were compared between UV and UV/PS, while emphasis was given on the effect of initial substrate concentration, PS dosage, and initial pH for the kinetics of AMT degradation by UV/PS. The main radical generated in the reaction were identified using the indirect method. The results showed that degradation of AMT by UV/PS was more cost-effective than UV alone . AMT degradation follows the first-order kinetic well (R2≥0.95), the persudo-first-order-constant kobs decreases with the increase of AMT concentration;the value of kobs was magnified gradually with the increasing PS dosage; controlling the pH of 5~10, kobs reaches the top of 0.0540min-1when pH=5; the main radical generated is ·SO4- when pH=7.
Keywords:persulfate  ametryn  impact factor  kinetic  
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