Receptor modeling of PM2.5, PM10 and TSP in different seasons and long-range transport analysis at a coastal site of Tianjin, China.

Abstract Atmospheric particulate matter (PM 2.5 , PM 10 and TSP) were sampled synchronously during three monitoring campaigns from June 2007 to February 2008 at a coastal site in TEDA of Tianjin, China. Chemical compositions including 19 elements, 6 water-solubility ions, organic and elemental carbon were determined. principle components analysis (PCA) and chemical mass balance modeling (CMB) were applied to determine the PM sources and their contributions with the assistance of NSS SO 4 2 − , the mass ratios of NO 3 − to SO 4 2 − and OC to EC. Air mass backward trajectory model was compared with source apportionment results to evaluate the origin of PM. Results showed that NSS SO 4 2 − values for PM 2.5 were 2147.38, 1701.26 and 239.80 ng/m 3 in summer, autumn and winter, reflecting the influence of sources from local emissions. Most of it was below zero in summer for PM 10 indicating the influence of sea salt. The ratios of NO 3 − to SO 4 2 − was 0.19 for PM 2.5 , 0.18 for PM 10 and 0.19 for TSP in winter indicating high amounts of coal consumed for heating purpose. Higher OC/EC values (mostly larger than 2.5) demonstrated that secondary organic aerosol was abundant at this site. The major sources were construction activities, road dust, vehicle emissions, marine aerosol, metal manufacturing, secondary sulfate aerosols, soil dust, biomass burning, some pharmaceutics industries and fuel-oil combustion according to PCA. Coal combustion, marine aerosol, vehicular emission and soil dust explained 5–31%, 1–13%, 13–44% and 3–46% for PM 2.5 , PM 10 and TSP, respectively. Backward trajectory analysis showed air parcels originating from sea accounted for 39% in summer, while in autumn and winter the air parcels were mainly related to continental origin.