the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Aerosol acidity in a megacity with high ambient temperature and relative humidity of Central China: temporal variation, determining factors and pollution transition effect
Abstract. Aerosol acidity affects the chemical transformation of aerosols and subsequent haze formation. High resolution (1-h) observation of water-soluble inorganic ions in fine particles, gaseous pollutants, and meteorological parameters was conducted from September 2015 to August 2016 at Wuhan, a megacity of Central China with high relative humidity and ambient temperature, compared with north Chinese cities. By adopting thermodynamic model ISOROPPIA-II, the aerosol acidity for different time scales, pollution episodes, and air mass directions was calculated. Aerosols in Wuhan were moderate acidic, with pH averaged as 3.30 ± 0.49. The aerosol acidity was higher in July (pH as 2.64 ± 0.31), September (pH as 2.75 ± 0.30) and August (pH as 2.79 ± 0.29), and lower in January (pH as 3.77 ± 0.28) and March (pH as 3.70 ± 0.16). It decreased with the air pollution increasing, with the pH values of 3.07 ± 0.45, 3.63 ± 0.27 and 3.84 ± 0.22 for clean, transition and polluted episodes, respectively. The air masses in Wuhan transported from North China exhibited higher aerosol acidity, with pH averaged as 3.17–3.22. The unique environmental and meteorological conditions (high humidity, annual averaged RH as 0.74 ± 0.13) lead to excess ammonium (on average of 6.06 ± 4.51 μg m−3) and abundant aerosol water content (AWC, on average of 71.0 ± 82.8 μg m−3) in Wuhan, which can explain the lower PM2.5 acidity in Wuhan than other megacities of China. At lower AWC level (less than ~ 15 μg m−3), the particle pH showed a decreasing trend with AWC increased. When the AWC continuous increased from ~ 15 to ~ 380 μg m−3, there was an obvious increase of particle pH. Then no significant growth of pH was found when AWC was higher than ~ 380 μg m−3. With atmospheric RH increasing, the aerosol pH exhibited decreasing trend firstly and then increased, with the turning point RH as about 0.48. There was a logarithmic growth of aerosol pH with total NHx (NH3 + NH4+) increasing. From the fitted logarithmic curve, the aerosol pH of Wuhan was at the range of pH rapid growth stage with NHx increasing, indicating that the control of ammonia emission in Wuhan could be an effective way to reduce the aerosol pH and further mitigate air pollution. This paper firstly obtained the aerosol acidity properties at a megacity under abundant ammonium and high humidity with high time-resolution, which is an important supplementary for the current aerosol acidity research around the world.
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Interactive discussion
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RC1: 'Review for the acp-2018-367', Anonymous Referee #1, 16 Jun 2018
- AC1: 'Response to Referee #1', Mingming Zheng, 31 Aug 2018
- AC2: 'Response to Referee', Mingming Zheng, 31 Aug 2018
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RC2: 'atmospheric chemistry', Anonymous Referee #2, 18 Jun 2018
- AC1: 'Response to Referee #1', Mingming Zheng, 31 Aug 2018
- AC2: 'Response to Referee', Mingming Zheng, 31 Aug 2018
Interactive discussion
-
RC1: 'Review for the acp-2018-367', Anonymous Referee #1, 16 Jun 2018
- AC1: 'Response to Referee #1', Mingming Zheng, 31 Aug 2018
- AC2: 'Response to Referee', Mingming Zheng, 31 Aug 2018
-
RC2: 'atmospheric chemistry', Anonymous Referee #2, 18 Jun 2018
- AC1: 'Response to Referee #1', Mingming Zheng, 31 Aug 2018
- AC2: 'Response to Referee', Mingming Zheng, 31 Aug 2018
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Cited
7 citations as recorded by crossref.
- Role of Ammonia on the Feedback Between AWC and Inorganic Aerosol Formation During Heavy Pollution in the North China Plain B. Ge et al. 10.1029/2019EA000799
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- Atmospheric emission inventory of SO3 from coal-fired power plants in China in the period 2009–2014 J. Shen et al. 10.1016/j.atmosenv.2018.10.008
- Parameterization of heterogeneous reaction of SO2 to sulfate on dust with coexistence of NH3 and NO2 under different humidity conditions S. Zhang et al. 10.1016/j.atmosenv.2019.04.004
- Estimating radiative impacts of black carbon associated with mixing state in the lower atmosphere over the northern North China Plain K. Hu et al. 10.1016/j.chemosphere.2020.126455
- Effect of aerosol radiative forcing uncertainty on projected exceedance year of a 1.5 °C global temperature rise A. Peace et al. 10.1088/1748-9326/aba20c
- Retrieval of surface PM2.5 mass concentrations over North China using visibility measurements and GEOS-Chem simulations S. Li et al. 10.1016/j.atmosenv.2019.117121