Humidity drives spontaneous OH oxidation of organic particles
Maria Angelaki, D. J. Donaldson, Sébastien Perrier, Matthieu Riva, C. George
Abstract
We report evidence that organic aerosols containing carboxylic acids can be spontaneously oxidized in the dark under normal atmospheric conditions due to interfacial hydroxyl radical production. Product formation is negligible under dry conditions and increases with increasing relative humidity. In a dioxygen-free environment, the oxidation efficiency is substantially decreased. Size-resolved measurements show an increase in the reactivity and product formation yields for smaller particles, correlated with their surface-to-volume ratio. Our findings suggest that spontaneous hydroxyl radical production at the air-water interface of organic nanodroplets may be an important pathway in their oxidation, especially during nighttime.