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      Seasonal characteristics, formation mechanisms and source origins of PM<sub>2.5</sub> in two megacities in Sichuan Basin, China

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          Abstract

          To investigate the characteristics of PM<sub>2.5</sub> and its major chemical components, formation mechanisms, and geographical origins in the two megacities, Chengdu (CD) and Chongqing (CQ), in Sichuan Basin of southwest China, daily PM<sub>2.5</sub> samples were collected simultaneously at one urban site in each city for four consecutive seasons from autumn 2014 to summer 2015. Annual mean concentrations of PM<sub>2.5</sub> were 67.0 ± 43.4 and 70.9 ± 41.4 µg m<sup>−3</sup> at CD and CQ, respectively. Secondary inorganic aerosol (SNA) and organic matter (OM) accounted for 41.1 and 26.1 % of PM<sub>2.5</sub> mass at CD, and 37.4 and 29.6 % at CQ, respectively. Seasonal variations of PM<sub>2.5</sub> and major chemical components were significant, usually with the highest mass concentration in winter and the lowest in summer. Daily PM<sub>2.5</sub> concentration exceeded the national air quality standard on 30 % of the sampling days at both sites, and most of the pollution events were at the regional scale within the basin formed under stagnant meteorological conditions. The concentrations of carbonaceous components were higher at CQ than CD, likely partially caused by emissions from the large number of motorcycles and the spraying processes used during automobile production in CQ. Heterogeneous reactions probably played an important role in the formation of SO<sub>4</sub><sup>2−</sup>, while both homogeneous and heterogeneous reactions contributed to the formation of NO<sub>3</sub><sup>−</sup>. Geographical origins of emissions sources contributing to high PM<sub>2.5</sub> masses at both sites were identified to be mainly distributed within the basin based on potential source contribution function (PSCF) analysis.

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          Secondary organic aerosol formation in cloud droplets and aqueous particles (aqSOA): a review of laboratory, field and model studies

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            Chemical characterization and source apportionment of PM2.5 in Beijing: seasonal perspective

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              Exploring the severe winter haze in Beijing: the impact of synoptic weather, regional transport and heterogeneous reactions

              Extreme haze episodes repeatedly shrouded Beijing during the winter of 2012–2013, causing major environmental and health problems. To better understand these extreme events, we performed a model-assisted analysis of the hourly observation data of PM 2.5 and its major chemical compositions. The synthetic analysis shows that (1) the severe winter haze was driven by stable synoptic meteorological conditions over northeastern China, and not by an abrupt increase in anthropogenic emissions. (2) Secondary species, including organics, sulfate, nitrate, and ammonium, were the major constituents of PM 2.5 during this period. (3) Due to the dimming effect of high loading of aerosol particles, gaseous oxidant concentrations decreased significantly, suggesting a reduced production of secondary aerosols through gas-phase reactions. Surprisingly, the observational data reveals an enhanced production rate of secondary aerosols, suggesting an important contribution from other formation pathways, most likely heterogeneous reactions. These reactions appeared to be more efficient in producing secondary inorganics aerosols than organic aerosols resulting in a strongly elevated fraction of inorganics during heavily polluted periods. (4) Moreover, we found that high aerosol concentration was a regional phenomenon. The accumulation process of aerosol particles occurred successively from cities southeast of Beijing. The apparent sharp increase in PM 2.5 concentration of up to several hundred μg m −3 per hour recorded in Beijing represented rapid recovery from an interruption to the continuous pollution accumulation over the region, rather than purely local chemical production. This suggests that regional transport of pollutants played an important role during these severe pollution events.
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                Author and article information

                Journal
                Atmospheric Chemistry and Physics
                Atmos. Chem. Phys.
                Copernicus GmbH
                1680-7324
                2018
                January 24 2018
                : 18
                : 2
                : 865-881
                Article
                10.5194/acp-18-865-2018
                35a639ab-3ca9-4f8a-8efe-1ff260b0ab70
                © 2018

                https://creativecommons.org/licenses/by/3.0/

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