4.7 Article

Inorganic aerosols responses to emission changes in Yangtze River Delta, China

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 481, Issue -, Pages 522-532

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.scitotenv.2014.02.076

Keywords

FM2.5; YRD; Inorganic aerosols sensitivity

Funding

  1. Energy Foundation [G-1208-16611]
  2. National Key Project of Basic Research of China [2006CB403704]
  3. National Natural Science Foundation of China [20877020, 40575062, 40599420]
  4. Office of Science of the U.S. Department of Energy, Regional and Global Climate Modeling Program
  5. Battelle Memorial Institute [DE-AC05-76RL01830]

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The new Chinese National Ambient Air Quality standards (CH-NAAQS) published on Feb. 29th, 2012 listed PM2.5 as criteria pollutant for the very first time. In order to probe into PM2.5 pollution over Yangtze River Delta, the integrated MM5/CMAQmodeling system is applied for a full year simulation to examine the PM2.5 concentration and seasonality, and also the inorganic aerosols responses to precursor emission changes. Total PM2.5 concentration over YRD was found to have strong seasonal variation with higher values in winter months (up to 89.9 mu g/m(3) in January) and lower values in summer months (down to 28.8 mu g/m(3) in July). Inorganic aerosols were found to have substantial contribution to PM2.5 over YRD, ranging from 37.1% in November to 52.8% in May. Nocturnal production of nitrate (NO3-) through heterogeneous hydrolysis of N2O5 was found significantly contribute to high NW concentration throughout the year. In winter, NO3- was found to increase under nitrogen oxides (NOx) emission reduction due to higher production of N2O5 from the excessive ozone (O-3) introduced by attenuated titration, which further lead to increase of ammonium (NH4+) and sulfate (SO42-), while other seasons showed decrease response of NO3- Sensitivity responses of NO3- under anthropogenic VOC emission reduction was examined and demonstrated that in urban areas over YRD, NO3- formation was actually more sensitive to VOC than NOx due to the O-3-involved nighttime chemistry of N2O5, while a reduction of NOx emission may have counter-intuitive effect by increasing concentrations of inorganic aerosols. (C) 2014 Elsevier B.V. All rights reserved.

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