Molecular characterization and volatility of organonitrates: Latest observations from field and laboratory

Here we show recent results from different field and laboratory campaigns focusing on organonitrate (ON) formation, mass concentration, and physicochemical properties such as volatility. ONs are formed via volatile organic compounds (VOC) and NO_x. They are therefore key species for our understanding of the interaction between the biosphere and anthropogenic activities, and the effects of altering both VOC and NO_x emissions due to climate change and/or air quality mitigation measures. Recently, we were able to show that ONs from different precursor VOC can also contribute significantly to the growth of newly formed particles in the atmosphere to sizes where they can become active and cloud condensation nuclei (Huang et al., 2019).

We present direct, real-time observations of ONs in the gas and particle phase at the highest atmospheric research station in the world, Chacaltaya (5240 m a. s. l) in Bolivia. This southern hemisphere station is often located in the free troposphere during night time, and influenced by the emissions from the nearby El Alto-La Paz metropolitan area, and biogenic emissions from surrounding forests as well as from the Amazon through long-range transport. ONs were measured using a Chemical Ionization Mass Spectrometer with a Filter Inlet for Gases and Aerosols. We observed hundreds of highly functionalized ONs with different molecular composition during day- and nighttime, indicating different sources and formation processes. A large contribution of the highly functionalized ONs was found especially during new particle formation events regularly observed at this location (Rose et al., 2015). Observations from the field will be compared to results from the Nitrate Aerosol and Volatility Experiment (NArVE) at the EUROCHAMP 2020 PACS-C3 smog chamber (PSI, Switzerland), where we investigated the ON fraction, chemical composition, and volatility of secondary organic aerosol (SOA) formed via nitrate radical initiated oxidation reactions of biogenic and anthropogenic VOC.