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建立 UV/过氧乙酸高级氧化工艺动力学模型。

Modeling the Kinetics of UV/Peracetic Acid Advanced Oxidation Process.

机构信息

School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.

出版信息

Environ Sci Technol. 2020 Jun 16;54(12):7579-7590. doi: 10.1021/acs.est.9b06826. Epub 2020 May 31.

DOI:10.1021/acs.est.9b06826
PMID:32396722
Abstract

Peracetic acid combined with UV (i.e., UV/PAA) has emerged as a novel advanced oxidation process (AOP) for water disinfection and micropollutant degradation, but kinetic modeling for this AOP was lacking. In this study, a comprehensive model was developed to elucidate the reaction mechanisms and simulate reaction kinetics of UV/PAA process. By combining radical scavenging experiments and kinetic modeling, accurate quantum yield of PAA under UV (Φ = 0.88 ± 0.04 mol-Einstein) was determined via simultaneously quenching OH and CHC(O)O with 2,4-hexadiene. The comparison between experimental observations and model predictions over a wide range of conditions allowed estimation of the rate constants of PAA with OH ( = 1.3 ± 0.2 × 10 M s) and HO ( ≤ 5 × 10 M s) with good accuracy. With derived Φ, and , the kinetic model accurately predicts PAA decay under UV photolysis across varying PAA and HO concentrations and water pH (5.8-7.2). Meanwhile, the model reveals that UV/PAA generates a lower OH concentration than UV/HO at equivalent oxidant concentrations, with CHC(O)OO as the most abundant carbon-centered radical. This study significantly improves the knowledge of reactive species generation and reaction kinetics and mechanisms under UV/PAA, and provides a useful kinetic model for this AOP in water treatment.

摘要

过氧乙酸与紫外线(即 UV/PAA)相结合,已成为一种用于水消毒和微污染物降解的新型高级氧化工艺(AOP),但该 AOP 的动力学模型仍存在空白。在本研究中,我们开发了一个综合模型,以阐明 UV/PAA 工艺的反应机制并模拟其反应动力学。通过自由基清除实验和动力学建模相结合,我们使用 2,4-己二烯同时猝灭 OH 和 CHC(O)O,确定了 PAA 在 UV 下的准确量子产率(Φ = 0.88 ± 0.04 mol-Einstein)。在广泛的条件范围内,将实验观察结果与模型预测进行比较,能够准确估计 PAA 与 OH(= 1.3 ± 0.2 × 10 M s)和 HO(≤ 5 × 10 M s)的反应速率常数。利用推导得出的 Φ、和,可以准确预测在不同 PAA 和 HO 浓度以及水 pH(5.8-7.2)条件下 PAA 在 UV 光解下的衰减。同时,该模型表明,在相同氧化剂浓度下,UV/PAA 产生的 OH 浓度低于 UV/HO,其中 CHC(O)OO 是最丰富的碳中心自由基。本研究显著提高了对 UV/PAA 条件下活性物种生成和反应动力学及机制的认识,并为该 AOP 在水处理中的应用提供了有用的动力学模型。

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