摘要
在磷酸盐缓冲液(PhosphateBuffer,PB)中考察了不同反应条件下臭氧(O3)降解阿特拉津(Atrazine,ATZ)的效果并对其氧化降解机理及氧化动力学进行探讨。结果表明,在pH7的PB中,恒温水浴20℃,ATZ、O3初始浓度分别为2.5、20μmol/L,反应时长20min时,O3对ATZ的降解率可达93%。机理分析表明,在O3降解ATZ过程中磷酸盐具有很好的缓冲效果且对O3分解无不良影响。反应体系pH值对O3降解ATZ有显著影响,在弱酸性条件下以直接氧化降解为主,氧化效果较弱;在弱碱性条件下以HO·氧化降解为主,氧化效果较强。动力学分析表明,O3降解ATZ动力学更为符合拟二级反应动力学。
The degradation of Atrazine (ATZ) by ozone (O 3) under different reaction conditions was investigated in Phosphate Buffer (PB). The oxidative degradation mechanism and oxidation kinetics were discussed. The results showed that in the PB of pH 7, the initial concentration of ATZ and O 3 was 2.5 and 20 μmol/L in the constant temperature water bath at 20°C, and the degradation rate of ATZ by O 3 was 93% in the reaction time of 20 min. The mechanism analysis showed that phosphate had a good buffering effect and no adverse effect on O 3 decomposition during O 3 degrading ATZ. The pH value of the reaction system has a significant effect on the degradation of ATZ by O 3. Under weakly acidic conditions, the direct oxidation degradation is dominant, and the oxidation effect is weak. Under weak alkaline conditions, HO·oxidative degradation is dominant, and the oxidation effect is stronger. Kinetic analysis showed that O 3 degrading ATZ kinetics was more consistent with pseudo-secondary reaction kinetics.
作者
丁张凯
陆一新
张建强
李红生
Ding Zhangkai;Lu Yixin;Zhang Jianqiang;Li Hongsheng(Hydrochina Mid-South Engineering & Consulting Co.,Ltd.,Changsha 410014;Faculty of Geosciences and Environmental Engineering, Southwest Jiaotong University, Chengdu 610031)
出处
《环保科技》
2019年第4期1-5,11,共6页
Environmental Protection and Technology
基金
四川省科技计划项目(2017GZ0375)
成都市科技惠民技术研发项目(2015-HM01-00333-SF)