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

Author:

Wang Junyue1ORCID,Schaefer Thomas2,Lisouskaya Aliaksandra3ORCID,Firak Daniele S2ORCID,Xin Xiaoyue1ORCID,Meng Lingjun1,Herrmann Hartmut2ORCID,Sharma Virender K4ORCID,Huang Ching-Hua1ORCID

Affiliation:

1. School of Civil and Environmental Engineering, Georgia Institute of Technology , 200 Bobby Dodd Way NW, Atlanta, GA 30332 , USA

2. Atmospheric Chemistry Department (ACD), Leibniz Institute for Tropospheric Research (TROPOS) , Permoserstraße 15, 04318 Leipzig , Germany

3. Radiation Laboratory, University of Notre Dame , 102 Radiaiton Research Building, Notre Dame, IN 46556 , USA

4. Department of Environment and Occupational Health, School of Public Health, Texas A&M University , 212 Adriance Lab Road, College Station, TX 77843 , USA

Abstract

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 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, the formation of CH3C(O)OO• was verified by spin-trapped electron paramagnetic resonance, 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−1 s−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.

Funder

U.S. National Science Foundation

Publisher

Oxford University Press (OUP)

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