To investigate the characteristics of water-soluble inorganic ions (WSIIs) in Chongqing, a well-known foggy and acid region in southwestern China, hourly real-time concentrations of five cations (Na+, K+, NH4+, Ca2+, and Mg2+) and six anions (F-, Cl-, NO2-, NO3-, PO43-, and SO42-) in PM2.5 during winter (from Dec. 18, 2015 to Mar. 20, 2016) in Chongqing were collected by applying In-situ Gas and Aerosol Compositions Monitor. The hourly total concentration of WSIIs was 38.5μg/m3 on average, accounting for 57% of PM2.5 mass concentration. Secondary inorganic aerosols (NH4+, NO3-, and SO42-) were dominant WSIIs, accounting for 91% of WSIIs mass. Compared to ten years ago, SO42- concentrations were decreased by 31% but NO3- levels were doubled, likely indicative of sharply enhanced contribution to fine particle pollution from mobile sources over stationary sources. NO3- originated from the current fluxes of NH3 and HNO3 onto sulfate particles and/or from in-cloud processes were critical pathways under humid conditions in the study area. Water content and/or RH might be important factors controlling nitrate formation. Trajectory analysis manifested that aerosol pollutions in Chongqing were mostly caused by local emissions.
Keywords: Formation mechanism; High time resolution; Particle acidity; Water-soluble ions.
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