Unveiling the environmental significance of acetylperoxyl radical: reactivity quantification and kinetic modeling

Junyue Wang, Thomas Schaefer, Aliaksandra Lisouskaya, Daniele S Firak, Xiaoyue Xin, Lingjun Meng, Hartmut Herrmann, Virender K Sharma, Ching-Hua Huang
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Abstract

Acetylperoxyl radical (CH3C(O)OO●) is among highly reactive organic radicals which are known to play crucial roles in atmospheric chemistry, aqueous chemistry and, most recently, peracetic acid (PAA)-based advanced oxidation processes. However, fundamental knowledge for its reactivity is scarce and severely hampers the understanding of relevant environmental processes. Herein, three independent experimental approaches were exploited for revelation and quantification of the reaction rates of acetylperoxyl radical. First, we developed and verified laser flash photolysis (LFP) of biacetyl, ultraviolet (UV) photolysis of biacetyl, and pulse radiolysis of acetaldehyde, each as a clean source of CH3C(O)OO●. Then, using competition kinetics and selection of suitable probe and competitor compounds, the rate constants between CH3C(O)OO● and compounds of diverse structures were determined. The three experimental approaches complemented in reaction time scale and ease of operation, and provided cross-validation of the rate constants. Moreover, formation of CH3C(O)OO● was verified by spin-trapped electron paramagnetic resonance (EPR), and potential influence of other reactive species in the systems was assessed. Overall, CH3C(O)OO● displays distinctively high reactivity and selectivity, reacting especially favorably with naphthyl and diene compounds (k ∼ 107-108 M-1s-1) but sluggishly with N- and S-containing groups. Significantly, we demonstrated that incorporating acetylperoxyl radical-oxidation reactions significantly improved the accuracy in modeling the degradation of environmental micropollutants by UV/PAA treatment. This study is among the most comprehensive investigation for peroxyl radical reactivity to date, and establishes a robust methodology for investigating organic radical chemistry. The determined rate constants strengthen kinetic databases and improve modeling accuracy for natural and engineered systems.
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揭示乙酰过氧自由基对环境的意义:反应性量化和动力学建模
乙酰过氧自由基(CH3C(O)OO●)是一种高活性有机自由基,在大气化学、水化学以及最近基于过乙酸(PAA)的高级氧化过程中发挥着至关重要的作用。然而,有关其反应性的基础知识非常匮乏,严重阻碍了对相关环境过程的了解。在此,我们采用了三种独立的实验方法来揭示和量化乙酰过氧自由基的反应速率。首先,我们开发并验证了生物乙酰的激光闪烁光解(LFP)、生物乙酰的紫外线(UV)光解和乙醛的脉冲辐射分解,每种方法都是 CH3C(O)OO● 的清洁来源。然后,利用竞争动力学并选择合适的探针和竞争化合物,测定了 CH3C(O)OO● 与不同结构的化合物之间的速率常数。这三种实验方法在反应时间范围和操作简便性方面互为补充,并对速率常数进行了交叉验证。此外,还通过自旋俘获电子顺磁共振(EPR)验证了 CH3C(O)OO● 的形成,并评估了体系中其他反应物的潜在影响。总之,CH3C(O)OO● 显示出明显的高反应性和选择性,与萘基和二烯化合物的反应尤其有利(k ∼ 107-108 M-1s-1),但与含 N 和 S 的基团的反应则较为迟缓。重要的是,我们证明了加入乙酰过氧自由基氧化反应可显著提高紫外线/PAA 处理环境微污染物降解模型的准确性。这项研究是迄今为止对过氧自由基反应性进行的最全面的研究之一,为研究有机自由基化学建立了一种可靠的方法。确定的速率常数加强了动力学数据库,提高了自然和工程系统建模的准确性。
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