Coupling of Lipid Peroxidation and Criegee Intermediate Mediated Autoxidation in the Heterogeneous Oxidation of Linoleic Acid Aerosols

Autoxidation is an established mechanism for the degradation of organic molecules, which is relevant in the atmosphere, combustion processes, the environment, and the rancidification of lipids (commonly known as lipid peroxidation). Autoxidation proceeds via radical chain reactions involving hydroxyl (<sup>•</sup>OH), peroxy (RO<sub>2</sub><sup>•</sup>), and alkoxy radicals, which are also prominent oxidants in the atmosphere. Recent reports have provided evidence for an alternative autoxidation mechanism driven instead by Criegee intermediates (CIs), which are produced from the reaction of β-hydroxy peroxy radicals (β-OH-RO<sub>2</sub><sup>•</sup>). This work evaluates the contributions of these two mechanisms in the <sup>•</sup>OH initiated heterogeneous oxidation of linoleic acid (LA) aerosols. Reaction kinetics and product distributions are monitored using a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer. To explain the observed kinetics, a kinetic model is developed that incorporates both the conventional peroxidation and alternative CI-mediated autoxidation mechanisms. We observe that the CI-mediated autoxidation pathways enhance the heterogeneous autoxidation rate, while the peroxidation reactions, although present, contributes less to the overall oxidation rate. α-Acyloxyalkyl hydroperoxides (AAHPs) are identified as key indicators for bimolecular reactions of CI with LA, highlighting the role of LA as a CI scavenger. Moreover, the measured functionalized LA products with hydroxyl or carbonyl group(s), serve as markers for the peroxidation reactions. In summary, this work presents a quantitative framework to understand the coupled reaction network of <sup>•</sup>OH, RO<sub>2</sub><sup>•</sup>, β-OH-RO<sub>2</sub><sup>•</sup> radicals, and CI in driving heterogeneous autoxidation, which is crucial for understanding degradation mechanisms of organic molecules in the environment and atmosphere.

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Publication Details

Journal
Environmental Science & Technology
Published
2025-05-01
DOI
https://doi.org/10.1021/acs.est.4c13472
Citations
2
Primary Topic
Water Quality Monitoring and Analysis
Type
article
Field-Weighted Citation Impact
1.99

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article

Coupling of Lipid Peroxidation and Criegee Intermediate Mediated Autoxidation in the Heterogeneous Oxidation of Linoleic Acid Aerosols

Meirong Zeng, Kevin R. Wilson
2 citations
Environmental Science & Technology
Water Quality Monitoring and Analysis
1.99
article

Coupling of Lipid Peroxidation and Criegee Intermediate Mediated Autoxidation in the Heterogeneous Oxidation of Linoleic Acid Aerosols

Meirong Zeng, Kevin R. Wilson
article en
2 citations

Abstract

Autoxidation is an established mechanism for the degradation of organic molecules, which is relevant in the atmosphere, combustion processes, the environment, and the rancidification of lipids (commonly known as lipid peroxidation). Autoxidation proceeds via radical chain reactions involving hydroxyl (<sup>•</sup>OH), peroxy (RO<sub>2</sub><sup>•</sup>), and alkoxy radicals, which are also prominent oxidants in the atmosphere. Recent reports have provided evidence for an alternative autoxidation mechanism driven instead by Criegee intermediates (CIs), which are produced from the reaction of β-hydroxy peroxy radicals (β-OH-RO<sub>2</sub><sup>•</sup>). This work evaluates the contributions of these two mechanisms in the <sup>•</sup>OH initiated heterogeneous oxidation of linoleic acid (LA) aerosols. Reaction kinetics and product distributions are monitored using a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer. To explain the observed kinetics, a kinetic model is developed that incorporates both the conventional peroxidation and alternative CI-mediated autoxidation mechanisms. We observe that the CI-mediated autoxidation pathways enhance the heterogeneous autoxidation rate, while the peroxidation reactions, although present, contributes less to the overall oxidation rate. α-Acyloxyalkyl hydroperoxides (AAHPs) are identified as key indicators for bimolecular reactions of CI with LA, highlighting the role of LA as a CI scavenger. Moreover, the measured functionalized LA products with hydroxyl or carbonyl group(s), serve as markers for the peroxidation reactions. In summary, this work presents a quantitative framework to understand the coupled reaction network of <sup>•</sup>OH, RO<sub>2</sub><sup>•</sup>, β-OH-RO<sub>2</sub><sup>•</sup> radicals, and CI in driving heterogeneous autoxidation, which is crucial for understanding degradation mechanisms of organic molecules in the environment and atmosphere.

Environmental Science & TechnologyVol. 59(18)
Lawrence Berkeley National Laboratory (US), Shanghai Jiao Tong University (CN), SMART Reading (US), NOAA Chemical Sciences Laboratory (US)
National Natural Science Foundation of China
Openalex Percentile: Top 14%
Water Quality Monitoring and Analysis
1.99
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