Abstract
Lipid peroxidation (autoxidation) is an established mechanism for the degradation of organic molecules in the atmosphere and the environment. Autoxidation proceeds via radical chain reactions involving hydroxyl (•OH), peroxy (RO2•), and alkoxy radicals, which are also prominent oxidants in the atmosphere. Recent reports have provided evidence for an alternative autoxidation mechanism driven instead by -hydroxy peroxy radicals (-OH-RO2•) and Criegee intermediates (CI). This work evaluates the contributions of these two mechanisms in the •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. Alpha-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 •OH, RO2•, -OH-RO2• radicals, and CI in driving heterogeneous autoxidation, which is crucial for understanding degradation mechanisms of organic molecules in the environment and atmosphere.
Supplementary materials
Title
Supporting Information
Description
Additional details regarding the experimental results and coupled autoxidation mechanisms are provided. Table S1 lists the reactions and their rate constants used in the present model. Figures S1-S5 showcase additional experimental and simulated profiles under various [•OH]. Meanwhile, Figures S6-S13 present further analyses into species identification and reaction pathways.
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