Back to Search Start Over

Contributions of local and regional anthropogenic sources of metals in PM2.5 at an urban site in northern France.

Authors :
Ledoux, Frédéric
Kfoury, Adib
Delmaire, Gilles
Roussel, Gilles
El Zein, Atallah
Courcot, Dominique
Source :
Chemosphere. Aug2017, Vol. 181, p713-724. 12p.
Publication Year :
2017

Abstract

PM 2.5 have been related to various adverse health effects, mainly due to their ability to penetrate deeply and to convey harmful chemical components, such as metals inside the body. In this work, PM 2.5 were sampled at Saint-Omer, a medium-sized city located in northern France, in March–April 2011 and analyzed for their total carbon, water-soluble ions, major and trace elements. More specifically, the origin of 15 selected elements was examined using different tools including enrichment factors, conditional bivariate probability function (CBPF) representations, diagnostic ratios and receptor modelling. The results indicated that PM 2.5 metal composition is affected by both emissions of a local glassmaking factory and an integrated steelworks located at a distance of 35 km from the sampling site. For the first time, diagnostic ratios were proposed for the glassmaking activity. Therefore, metals in PM 2.5 could be attributed to the following anthropogenic sources: (i) local glassmaking industry for Sn, As, Cu and Cr, (ii) distant integrated steelworks for Ag, Fe, Cd, Mn, Rb and Pb, (iii) heavy fuel oil combustion for Ni, V and Co and (iv) non-exhaust traffic for Zn, Pb, Mn, Sb, and Cu. The impact of such sources on metal concentrations in PM 2.5 was assessed using a constrained receptor model. Despite their low participation to PM 2.5 concentration (2.7%), the latter sources were found as the main contributors (80%) to the overall concentration levels of the 15 selected elements in PM 2.5 . [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
181
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
123042850
Full Text :
https://doi.org/10.1016/j.chemosphere.2017.04.128