RESUMO
Latin American (LatAm) cities are grappling with elevated levels of gaseous and particulate pollutants, which are having detrimental effects on both the local ecosystem and human health. Of particular concern are aerosols with smaller diameters (lower or equal to 2.5 µm, PM2.5), known for their ability to penetrate deep into the respiratory system. While measurements in the region are increasing, they remain limited. This study addresses this gap by presenting the results of a comprehensive, year-long PM2.5 monitoring campaign conducted in six LatAm cities: Buenos Aires, São Paulo, Medellín, San José, Quito and Ciudad de México. Despite all six monitoring sites being urban, they exhibited significant variations in PM2.5 levels, as well as in the content and seasonal behavior of elemental carbon (EC) and organic carbon (OC). Estimations of secondary organic carbon (SOC) using the EC-tracer method revealed a notable SOC relevance across all cities: secondary organic aerosols (SOA) accounted in average for between 19 % to 48 % of the total carbonaceous matter. Source attribution, conducted through the Positive Matrix Factorization (PMF) model, highlights substantial contributions from gasoline and diesel traffic emissions (29 % to 49 % of total carbon, TC), regional biomass burning (21 % to 27 %), and SOA (20 % to 38 %) in all cities, with similar chemical signatures. Additionally, industrial emissions were significant in two cities (Medellín and San José), while two others experienced minor impacts from construction machinery at nearby sites (Buenos Aires and Quito). This comparative analysis underscores the importance of considering not only the thermal optical EC/OC fractions as tracers of sources but also the OC/EC ratio of the PMF factors. This dual approach not only adds depth to the research but also suggests varied methodologies for addressing this crucial environmental concern. This study lays the groundwork for future investigations into the factors influencing the content and seasonality of SOA in the region.
RESUMO
ABSTRACT The present work shows the results of a first study aimed at determining the elemental composition in airborne particulate matter (in fine and coarse particle size fractions). It was collected at the Atmospheric Monitoring Station in the Municipality of Centro Habana, using the Particle Induced Xray Emission (PIXE) technique. At present, there is no information available about elemental contents in airborne particulate matter from this region. For this study, we carried out a sampling campaign during five months (November 14, 2006 to April 19, 2007). The samples were collected every second day during 24 h under an air flux of 20 l/min. The air sampler used was a Gent Sampler equipped with a Stacked Filter Unit (SFU) system which allows the aerosol collection in both size fractions simultaneously. A total of 144 aerosol samples were collected (72 correspond to the fine mass particle and 72 to the coarse mass particle). For PIXE analysis, the samples were irradiated by 2.0 MeV energy protons from the 2 MV Tandetron Accelerator from the Laboratory of PIXE analysis at ININ, Mexico. A total of 14 elements (S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br and Pb) were consistently detected in both of particle size fractions with minimum detection limits in the range of 1-10 ng/
. The quantitative results obtained from PIXE elemental analysis for mass of particles in both fractions have revealed important information that has been used in a first attempt to understand and characterize the atmospheric pollution in this area. A general discussion about these results is presented in this paper.
RESUMEN El presente trabajo reporta los resultados de un primer estudio realizado para determinar la composición elemental en material particulado atmosférico (en tamaños de partícula fina y gruesa) colectado en la Estación de Monitoreo Ambiental del Instituto Nacional de Higiene y Epidemiología, del Municipio de Centro Habana, utilizando la técnica PIXE (emisión de rayos X inducida por partículas). Para este estudio se realizó una campaña de muestreo durante cinco meses, entre los meses de noviembre, 2006 y abril, 2007, con un período de colección de una toma cada segundo día y 24 horas de duración. Se utilizó un muestreador de aire del tipo Gent con posibilidades de colectar de forma simultánea el material particulado fino y grueso. Un total de 144 muestras de MPA se colectaron para este estudio (72 de fracción fina y 72 de fracción gruesa). Las muestras se irradiaron tras la incidencia de un haz de protones de 2,5 MeV. Un total de 14 elementos (S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br y Pb) fueron consistentemente detectados en la mayoría de las muestras, con límites mínimos de detección entre 1-10 ng de partículas/ de aire. Los resultados del análisis PIXE para ambos tamaños de partícula revelaron una importante información que se ha utilizado en una primera intención para entender y caracterizar la contaminación atmosférica del área muestreada. Se presenta una discusión general de estos resultados en este trabajo.
