Journal
ATMOSPHERIC ENVIRONMENT
Volume 149, Issue -, Pages 70-83Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.atmosenv.2016.10.049
Keywords
Aerosols; Lead isotopes; TIMS; Urban pollution; Megacities; Brazil
Funding
- FAPESP [04/15277-9]
- Imperial College London
- Natural Environment Research Council [NE/H005390/1] Funding Source: researchfish
- NERC [NE/H005390/1] Funding Source: UKRI
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [04/15277-9] Funding Source: FAPESP
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Atmospheric lead (Pb) concentrations in Sao Paulo city, Brazil, remain significant, despite the fact that leaded gasoline was phased out. The use of its isotope signature allows tracing emissions to the increasing number of cars, urban construction, and industrial emissions in this densely populated area. High-precision and accurate stable isotope ratio determinations using isotope dilution thermal ionization mass spectrometry (ID-TIMS) combined with particle induced X-ray emission (PIXE) and multivariate analysis were used to identify the main sources of lead present in Sao Paulo atmospheric particulates. Throughout a period of sixty days, aerosol samples were collected every 12 h during the summer of 2005 at the University of Sao Paulo (USP) and simultaneously during one week in an industrial area (Cubatao) and in two more remote areas (Sao Lourenco da Serra and Juquitiba). The data suggests that aerosols from Sao Paulo are mainly derived from vehicular exhaust (mostly gasoline) and traffic dust resuspension, with the admixture of industrial emissions, including cement. Lead isotopic compositions (expressed as Pb-206/Pb-207 ratios) measured in Sao Paulo aerosols range from 1.1491 to 1.2527 and are similar to those determined from tunnel dust, fuels, and vehicular exhaust; therefore, those are likely to be the main lead sources in the atmosphere of sao Paulo. Vehicular traffic (fuel combustion, dust from vehicular components, and road dust) remains an important source of lead in the atmosphere. The maximum concentration occurring during the summer was 0.055 mu g m(-3) in fine particles, which is detrimental for human health and may lead to exceedances of the Air Quality Standard for lead of 0.15 mu g m(-3) (3-month average) during other seasons when the dispersion of pollutants is less favourable. (C) 2016 Elsevier Ltd. All rights reserved.
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