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

Acetylperoxyl radical (CH<sub>3</sub>C(O)OO<sup>•</sup>) 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 of biacetyl, ultraviolet (UV) photolysis of biacetyl, and pulse radiolysis of acetaldehyde, each as a clean source of CH<sub>3</sub>C(O)OO<sup>•</sup>. Then, using competition kinetics and selection of suitable probe and competitor compounds, the rate constants between CH<sub>3</sub>C(O)OO<sup>•</sup> 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, the formation of CH<sub>3</sub>C(O)OO<sup>•</sup> was verified by spin-trapped electron paramagnetic resonance, and potential influence of other reactive species in the systems was assessed. Overall, CH<sub>3</sub>C(O)OO<sup>•</sup> displays distinctively high reactivity and selectivity, reacting especially favorably with naphthyl and diene compounds (<i>k</i> ∼ 10<sup>7</sup>-10<sup>8</sup> M<sup>-1</sup> s<sup>-1</sup>) 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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Publication Details

Journal
PNAS Nexus
Published
2024-08-01
DOI
https://doi.org/10.1093/pnasnexus/pgae330
Citations
14
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
2.82

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article

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

Virender K. Sharma, Hartmut Herrmann, Aliaksandra Lisouskaya, Thomas Schaefer et al.
14 citations
PNAS Nexus
Advanced oxidation water treatment
2.82
article

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

Virender K. Sharma, Hartmut Herrmann, Aliaksandra Lisouskaya, Thomas Schaefer, Xiaoyue Xin, Ching‐Hua Huang, Junyue Wang, Daniele Scheres Firak, Lingjun Meng
article en
14 citations

Abstract

Acetylperoxyl radical (CH<sub>3</sub>C(O)OO<sup>•</sup>) 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 of biacetyl, ultraviolet (UV) photolysis of biacetyl, and pulse radiolysis of acetaldehyde, each as a clean source of CH<sub>3</sub>C(O)OO<sup>•</sup>. Then, using competition kinetics and selection of suitable probe and competitor compounds, the rate constants between CH<sub>3</sub>C(O)OO<sup>•</sup> 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, the formation of CH<sub>3</sub>C(O)OO<sup>•</sup> was verified by spin-trapped electron paramagnetic resonance, and potential influence of other reactive species in the systems was assessed. Overall, CH<sub>3</sub>C(O)OO<sup>•</sup> displays distinctively high reactivity and selectivity, reacting especially favorably with naphthyl and diene compounds (<i>k</i> ∼ 10<sup>7</sup>-10<sup>8</sup> M<sup>-1</sup> s<sup>-1</sup>) 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.

PNAS NexusVol. 3(8)
University of Notre Dame (US), Georgia Institute of Technology (US), Leibniz Institute for Tropospheric Research (DE), Texas A&M University (US)
National Science Foundation, U.S. Department of Energy, Office of Science, Division of Chemistry, Basic Energy Sciences
Openalex Percentile: Top 10%
Advanced oxidation water treatment
2.82
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