4.5 Article

The composition of PM1 and PM2.5 samples, metals and their water soluble fractions in the Bologna area (Italy)

Journal

ATMOSPHERIC POLLUTION RESEARCH
Volume 6, Issue 4, Pages 708-718

Publisher

TURKISH NATL COMMITTEE AIR POLLUTION RES & CONTROL-TUNCAP
DOI: 10.5094/APR.2015.079

Keywords

PM2.5; PM1; water soluble metals; air quality; waste incinerator

Funding

  1. Emilia-Romagna Region
  2. Regional Agency for Prevention and Environment

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In this study the metal composition of PM1 and PM2.5 samples collected in the surroundings of a municipal incinerator located in a suburban-farming area, less than 10 km away from Northeast of Bologna (Italy) was investigated. Seven out of eight monitoring stations were installed in a domain of 8x9 km(2) around the incinerator plant; the eighth station was placed inside the urban area of Bologna. The coordinates of four monitoring stations were selected on the basis of a preliminary study by using a dispersion model. Eleven metals (Al, Sb, As, Cd, Fe, Mn, Ni, Pb, Cu, V, Zn) were quantified in both the filter acid-digests and in the water extracts. The PM2.5 collected in all the sites of the domain were highly correlated with exception of the urban site. The daily average metal concentrations in summer were 1.84% and 1.14% for PM2.5 and PM1 respectively, indicating that fine particles are less enriched in metals. Fe, Al and Zn were the most abundant elements, and they represented about the 80% of the total amount of the analyzed ones. The average water soluble metal compositions were 0.71% and 0.41% for PM2.5 and PM1 respectively. In the sites of the suburban-farming studied area the Principal Component Analysis (PCA) and Cluster Analysis revealed differences between water soluble metal compositions in PM1 and PM2.5. The urban sites were characterized by lower total and soluble metals contents than the other PM2.5 stations installed around the incinerator plant. However, no noticeable difference in the concentrations of metals in the particulate matter between the sites chosen as maxima of incinerator emissions and the control sites was observed.

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