4.7 Article

Mixing state of ambient aerosols during different fog-haze pollution episodes in the Yangtze River Delta, China

Journal

ATMOSPHERIC ENVIRONMENT
Volume 178, Issue -, Pages 1-10

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.atmosenv.2018.01.032

Keywords

Mixing state; Fog-haze; Single particle aerosol mass spectrometer; The Yangtze River Delta

Funding

  1. National Natural Science Foundation of China [91644224, 41575132]
  2. National Key Research and Development Program of China [2016YFA0602003]
  3. Startup Foundation for Introducing Talent of NUIST [2016r040]
  4. open fund by the Key Laboratory for Aerosol-Cloud-Precipitation of CMA-NUIST [KDW1705]

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The mixing state of aerosol particles were investigated using a single particle aerosol mass spectrometer (SPAMS) during a regional fog-haze episode in the Yangtze River Delta (YRD) on 16-28 Dec., 2015. The aerosols were analyzed and clustered into 12 classes: aged elemental carbon (Aged-EC), internally mixed organics and elemental carbon (ECOC), organic carbon (OC), Biomass, Amine, Ammonium, Na-K, V-rich, Pb-rich, Cu-rich, Fe rich and Dust. Results showed that particles in short-term rainfalls mixed with more nitrate and oxidized organics, while they mixed with more ammonium and sulfate in long-term rainfall. Due to anthropogenic activities, stronger winds and solar radiation, the particle counts increased and the size ranges of particles broadened in haze. Carbonaceous particles and Na-K mixed with enhanced secondary species during haze, and obviously were more acidic, especially for the ones with a size range of 0.6-1.2 mu m. For local and long-range transported pollution, OC had distinct size distributions while the changes of ECOC were uniform. The secondary formation of ECOC contributed significantly in local pollution and affected much smaller particles (as small as 0.5 mu m) in long-range transported pollution. And long-range transported pollution was more helpful for the growth of OC. Particles mixed with more chloride and nitrate/sulfate in local/long-range transported pollution.

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