Physical and chemical properties of urban aerosols in São Paulo, Brazil: links between composition and size distribution of submicron particles

• Published in: Atmospheric chemistry and physics 2021-06, Vol.21 (11), p.8761-8773
• Main Authors: Monteiro dos Santos, Djacinto, Rizzo, Luciana Varanda, Carbone, Samara, Schlag, Patrick, Artaxo, Paulo
• Format: Article
• Language: English
• Subjects: Accumulation; Aerosols; Air pollution; Air quality; Algorithms; Anthropogenic factors; Atmospheric aerosols; Atmospheric sciences; Biodiesel fuels; Biofuels; Biomass burning; Black carbon; Burning; Chemical composition; Chemical properties; Chemical speciation; Chemicophysical properties; Condensates; Efficiency; Emissions; Gases; Geophysics; Hydrocarbons; Mass; Megacities; Metropolitan areas; Modes; Nucleation; Optical properties; Particle size distribution; Particulate emissions; Pollutants; Radiation; Regression analysis; Secondary aerosols; Size distribution; Speciation; Time series; Urban areas; Urban environments; Variables; Vehicle emissions
• ISSN: 1680-7324; 1680-7316; 1680-7324
• DOI: 10.5194/acp-21-8761-2021

In this work, the relationships between size and composition of submicron particles (PM1) were analyzed at an urban site in the Metropolitan Area of São Paulo (MASP), a megacity with about 21 million inhabitants. The measurements were carried out from 20 December 2016 to 15 March 2017. The chemical composition was measured with an Aerodyne Aerosol Chemical Speciation Monitor and size distribution with a TSI Scanning Mobility Particle Sizer 3082. PM1 mass concentrations in the MASP had an average mass concentration of 11.4 µg m−3. Organic aerosol (OA) dominated the PM1 composition (56 %), followed by sulfate (15 %) and equivalent black carbon (eBC, 13 %). Four OA classes were identified using positive matrix factorization: oxygenated organic aerosol (OOA, 40 % of OA), biomass burning organic aerosol (BBOA, 13 %), and two hydrocarbon-like OA components (a typical HOA related to vehicular emissions (16 %) and a second HOA (21 %) representing a mix of anthropogenic sources). Particle number concentrations averaged 12 100±6900 cm−3, dominated by the Aitken mode. The accumulation mode increased under relatively high-PM1 conditions, suggesting an enhancement of secondary organic aerosol (SOA) production. Conversely, the contribution of nucleation-mode particles was less dependent on PM1 levels, consistent with vehicular emissions. The relationship between aerosol size modes and PM1 composition was assessed by multilinear regression (MLR) models. Secondary inorganic aerosols were partitioned between Aitken and accumulation modes, related to condensation particle growth processes. Submicron mass loading in the accumulation mode was mostly associated with highly oxidized OOA and also traffic-related emissions. To the authors' knowledge, this is the first work that uses the MLR methodology to estimate the chemical composition of the different aerosol size modes. The chemical composition with size-dependent PM provides innovative information on the properties of both primary and secondary organic aerosols, as well as inorganic aerosols in a complex urban environment. The results emphasize the relevance of vehicular emissions to the air quality at MASP and highlight the key role of secondary processes on the PM1 ambient concentrations in the region since 56 % of PM1 mass loading was attributed to SOA and secondary inorganic aerosol.