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Chemical composition of ambient particulate matter and redox activity.

Authors :
Hueiwang Anna Jeng
Source :
Environmental Monitoring & Assessment; Oct2010, Vol. 169 Issue 1-4, p597-606, 10p
Publication Year :
2010

Abstract

Exposure to ambient particulate matter (PM) has been associated with a number of adverse health effects. Increasing studies have suggested that such adverse health effects may derive from oxidative stress, initiated by the formation of reactive oxygen species (ROS) within affected cells. The study aimed to assess physical characteristics and chemical compositions of PM and to correlate the results to their redox activity. PM (mass aerodynamic diameter ≤2.5 μm) and ultrafine particles (UFPs, mass media aerodynamic diameter <0.1 μm) were collected in an urban area, which had heavy traffic and represented ambient air pollution associated with vehicle exhaust. Background samples were collected in a rural area, with low traffic flow. Organic carbon (OC), elemental carbon (EC), polycyclic aromatic hydrocarbons (PAHs), and metals were analyzed. The dithiothreitol activity assay was used to measure the redox activity of PM. Results showed that UFPs have higher concentrations of OC, EC, and PAHs than those of PM. Several metals, including Fe, Cu, Zn, Ti, Pb, and Mn, were detected. Among them, Cu had the highest concentrations, followed by Fe and Zn. Organic carbon constituted 22.8% to 59.7% of the content on the surface of PM and UFPs. Our results showed higher redox activity on a per PM mass basis for UFPs as compared to PM. Linear multivariable regression analyses showed that redox activity highly correlated with PAH concentrations and organic compounds, and insignificantly correlated with EC and metals, except soluble Fe, which increased redox activity in particle suspension due to the presence of ROS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01676369
Volume :
169
Issue :
1-4
Database :
Complementary Index
Journal :
Environmental Monitoring & Assessment
Publication Type :
Academic Journal
Accession number :
53443406
Full Text :
https://doi.org/10.1007/s10661-009-1199-8