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Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion
Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion
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Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion
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Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion
Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion

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Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion
Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion
Journal Article

Variation of the Distribution of Atmospheric n-Alkanes Emitted by Different Fuels’ Combustion

2020
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Overview
This study presents the emission profiles of n-alkanes for different vehicular sources in two Brazilian cities. Atmospheric particulate matter was collected in São Paulo (Southeast) and in Salvador (Northeast) to determine n-alkanes. The sites were impacted by bus emissions and heavy and light-duty vehicles. The objective of the present study is to attempt to differentiate the profile of n-alkane emissions for particulate matter (PM) collected at different sites. PM concentrations ranged between 73 and 488 µg m−3, and the highest concentration corresponded to a tunnel for light and heavy duty vehicles. At sites where diesel-fueled vehicles are dominant, the n-alkanes show a unimodal distribution, which is different from the bimodal profile observed in the literature. Carbon preference index values corresponded to anthropogenic sources for most of the sites, as expected, but Cmax varied comparing to literature and a source signature was difficult to observe. The main sources to air pollution were indicated by principal component analysis (PCA). For PCA, a receptor model often used as an exploratory tool to identify the major sources of air pollutant emissions, the principal factors were attributed to mixed sources and to bus emissions. Chromatograms of four specific samples showed distinct profiles of unresolved complex mixtures (UCM), indicating different contributions of contamination from petroleum or fossil fuel residues, which are unable to resolve by gas chromatography. The UCM area seemed higher in samples collected at sites with the abundance of heavy vehicles.