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臭氧氧化和臭氧与过氧化氢联合氧化两种农药在天然水中的动力学研究。

Oxidation kinetics of two pesticides in natural waters by ozonation and ozone combined with hydrogen peroxide.

机构信息

Department of Civil and Environmental Engineering, Markin/CNRL Natural Resources Engineering Facility, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Water Res. 2011 Apr;45(8):2517-26. doi: 10.1016/j.watres.2011.02.007. Epub 2011 Feb 12.

Abstract

The oxidation of bromoxynil and trifluralin was investigated using ozone (O(3)) and O(3) combined with hydrogen peroxide (H(2)O(2)) in natural waters using batch reactors. The results indicated that these pesticides could not be completely degraded during ozonation, achieving degradation levels lower than 50%. An enhancement of the level of degradation was observed using O(3)/H(2)O(2) process. A biphasic behaviour of O(3) was also observed. Depending on the experimental conditions, the rate constant for O(3) decomposition was estimated to be between 7.4 × 10(-4) s(-1) to 5.8 × 10(-2) s(-1), and 3.2 × 10(-3) s(-1) to 4.2 × 10(-2) s(-1) for bromoxynil and trifluralin samples, respectively. Acute toxicity analysis performed using Microtox(®) showed a decrease in the toxic effects of the samples on the luminescent bacteria during the first few minutes of treatment, followed by an increase of the toxic effects at the end of the reaction for both pesticides. The quantification of oxidation by-products generated during treatment was also addressed. The total molar balances of the degradation by-products versus the initial pesticide concentrations ranged from 60 to 103% under different experimental conditions.

摘要

采用批式反应器,在天然水体中使用臭氧(O(3))和臭氧与过氧化氢(H(2)O(2))组合对溴苯腈和氟乐灵的氧化作用进行了研究。结果表明,这些农药在臭氧氧化过程中不能完全降解,降解水平低于 50%。使用 O(3)/H(2)O(2)工艺可提高降解水平。还观察到臭氧的两相行为。根据实验条件,O(3)分解的速率常数估计分别为 7.4×10(-4)s(-1)至 5.8×10(-2)s(-1)和 3.2×10(-3)s(-1)至 4.2×10(-2)s(-1),对于溴苯腈和氟乐灵样品。使用 Microtox(®)进行的急性毒性分析表明,在处理的最初几分钟内,样品对发光细菌的毒性作用降低,随后在反应结束时毒性作用增加。还解决了处理过程中生成的氧化副产物的定量问题。在不同实验条件下,降解副产物相对于初始农药浓度的总摩尔平衡范围为 60%至 103%。

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