Primary and secondary organic aerosol in an urban/industrial site: Sources, health implications and the role of plastic enriched waste burning.

PM10 samples were collected from an urban/industrial site nearby Athens, where uncontrolled burning activities occur. PAHs, monocarboxylic, dicarboxylic, hydroxycarboxylic and aromatic acids, tracers from BVOC oxidation, biomass burning tracers and bisphenol A were determined. PAH, monocarboxylic acids, biomass burning tracers and bisphenol A were increased during autumn/winter, while BSOA tracers, dicarboxylic- and hydroxycarboxylic acids during summer. Regarding aromatic acids, different sources and formation mechanisms were indicated as benzoic, phthalic and trimellitic acids were peaked during summer whereas p-toluic, isophthalic and terephthalic were more abundant during autumn/winter. The Benzo[a]pyrene-equivalent carcinogenic power, carcinogenic and mutagenic activities were calculated showing significant (p < 0.05) increases during the colder months. Palmitic, succinic and malic acids were the most abundant monocarboxylic, dicarboxylic and hydrocarboxylic acids during the entire sampling period. Isoprene oxidation was the most significant contributor to BSOA as the isoprene-SOA compounds were two times more abundant than the pinene-SOA (13.4 ± 12.3 and 6.1 ± 2.9 ng/m3, respectively). Ozone has significant impact on the formation of many studied compounds showing significant correlations with: isoprene-SOA (r = 0.77), hydrocarboxylic acids (r = 0.69), pinene-SOA (r = 0.63),dicarboxylic acids (r = 0.58), and the sum of phthalic, benzoic and trimellitic acids (r = 0.44). PCA demonstrated five factors that could explain sources including plastic enriched waste burning (30.8%), oxidation of unsaturated fatty acids (23.0%), vehicle missions and cooking (9.2%), biomass burning (7.7%) and oxidation of VOCs (5.8%). The results highlight the significant contribution of plastic waste uncontrolled burning to the overall air quality degradation.

[Secondary Aerosol Formation in Urban Shanghai: Insights into the Roles of Photochemical Oxidation and Aqueous-Phase Reaction].

Secondary species are one of the most important components of PM1 particles. To investigate the contributions as well as the factors that affect the formation of the secondary aerosols, a high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS, AMS) was employed to characterize sub-micron particles (PM1) during spring and summer in urban Shanghai. Organics were dominant in PM1 particles and comprised around 55% of the total PM1 mass concentration, followed by sulfate (24%) and nitrate (10%). Positive matrix factorization was further applied to explore the sources of the organics. It was found that primary and secondary organic aerosols accounted for around 34% and 66% of the total organics, respectively. Three episodes were observed during the measurements, where secondary species increased substantially. Increases of secondary species were represented by increases of sulfate and LV-OOA1 in spring, especially during the noontime, thus indicating that their formation is promoted by photochemical oxidation; yet in summer, photochemical and aqueous chemistry together accelerate the formation of secondary species, as indicated by the good correlations between nitrate and aerosol liquid water as well as between SOA and Ox. Overall, we found that contributions from secondary organic and inorganic aerosols to total PM1 particles were 35.5% and 43%, respectively. This study highlights that the influence of photochemical and aqueous chemistry is significant in the promotion of secondary species formation in Shanghai.