Fujian Provincial Meteorological Bureau

Fuzhou, China

Fujian Provincial Meteorological Bureau

Fuzhou, China
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Wang H.,Nanjing University of Information Science and Technology | An J.,Nanjing University of Information Science and Technology | Zhu B.,Nanjing University of Information Science and Technology | Shen L.,Jiaxing Environmental Monitoring Station | And 2 more authors.
Atmosphere | Year: 2017

In order to investigate the size distributions and seasonal variations of carbonaceous aerosols (organic carbon (OC) and elemental carbon (EC)), the carbonaceous species were collected in Nanjing, a typical industrial city located in Yangtze River Delta, China, in the summer, autumn, and winter of 2013 and spring of 2014, and then analyzed by using a 9-stage Anderson-type aerosol sampler and DRI Model 2001A Thermal/Optical Carbon Analyzer. OC, EC, secondary organic carbon (SOC), and primary organic carbon (POC) exhibited obvious seasonal variations, with the highest levels in winter (39.1 ± 14.0, 5.7 7 ± 2.1, 23.6 ± 11.7, and 14.1 ± 5.7 μg·m-3, respectively) and the lowest levels in summer (20.6 ± 6.7, 3.3 ± 2.0, 12.2 ± 3.8 and 8.4 ± 4.1 μg·m-3, respectively), and were mainly centralized in PM1.1 in four seasons. The concentrations of OC in PM1.1 varied in the order of winter > autumn > spring > summer, while EC ranked in the order of autumn > winter > summer > spring. In the PM1.1-2.1 and PM2.1-10, the concentrations of OC and EC decreased in the sequence of winter > spring > autumn > summer. The size spectra of OC, EC, and SOC had bimodal distributions in four seasons, except for EC with four peaks in summer. The size spectra of POC varied greatly with seasons, exhibiting bimodal distribution in winter, trimodal distribution in spring and summer, and four peaks in autumn. The OC/EC ratios were 7.0, 6.3, 7.6, and 6.9 in spring, summer, autumn and winter, respectively, which demonstrated the abundance of secondary organic aerosols in Nanjing. The sources of carbonaceous aerosol varied significantly with seasons, and were dominated by vehicle exhaust, and coal and biomass burning in PM2.1, and dominated by dust, and coal and biomass burning in PM2.1-10. © 2017 by the authors. Licensee MDPI, Basel, Switzerland.

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