Oxidation of Phenolic Aldehydes by Ozone and Hydroxyl Radicals at the Air–Solid Interface

[Image: see text] Biomass burning emissions contain abundant phenolic aldehydes (e.g., syringaldehyde, vanillin, and 4-hydroxybenaldehyde) that are oxidized during atmospheric transport, altering the physicochemical properties of particulates. Herein, the oxidative processing of thin films made of syringaldehyde, vanillin, and 4-hydroxybenaldehyde is studied at the air–solid interface under a variable O(3)(g) molar ratio (410 ppbv–800 ppmv) and relative humidity (0–90%). Experiments monitored the absorption changes of C=C, C=O, and —COOH vibration changes during the oxidation of thin films by transmission Fourier transform infrared spectroscopy (FTIR). Selected spectroscopic features of aromatic ring cleavage by O(3)(g) revealed the production of carboxylic acids. Instead, monitoring O—H stretching provided a comparison of a hydroxylation channel from in situ produced hydroxyl radical. The overall oxidation reactivity trend syringaldehyde > vanillin > 4-hydroxybenzladehyde can be explained based on the additional electron density from methoxide substituents to the ring. The reactive uptake coefficient of O(3)(g) increases for higher relative humidity, e.g., for syringaldehyde by 18 and 215 times at 74% and 90% relative humidity (RH), respectively, as compared to dry conditions. A Langmuir–Hinshelwood mechanism fits well the kinetics of oxidation under a variable O(3)(g) molar ratio at 74% RH, providing useful information that should be included in atmospheric chemistry models.