Abstract. To understand the impact of firework-burning (FW) particles on air quality and human health during the winter haze period, 39 elements, 10 water-soluble ions and 8 fractions of carbonaceous species in atmospheric PM2.5 in Nanjing were investigated during the 2014 Chinese Spring Festival (SF). Serious regional haze pollution persisted throughout the entire sampling period, with PM2.5 averaging at 113 ± 69 μg m−3 and visibility at 4.8 ± 3.2 km. The holiday effect led to almost all the chemical species decreasing during the SF, except for Al, K, Ba and Sr which were related to FW. The source contributions of coal combustion, vehicle emission and road dust decreased dramatically, whereas FW contributed to about half of the PM2.5 during the SF period. The intensive emission of FW particles on New Year's Eve accounted for 60.1% of the PM2.5. Fireworks also obviously modified the chemical compositions of PM2.5, with 39.3% contributed by increased organic matter, followed by steadily increased loadings of secondary inorganic ions. The aging processes of the FW particles lasted for about 4 days reflected by the variations of Ba, Sr, NH4+, NO3−, SO42− and K+, characterized by heterogeneous reactions of SO2 and NOx on crustal materials directly from FW, the replacement of Cl− by NO3− and SO42−, coating of NO3− and SO42− on soot, formation of secondary organic aerosols and metal-catalyzed formation of NO3− and SO42− at higher relative humidity. During aging, the main contributors to the extinction coefficient shifted from elemental carbon and organic matter to ammonium sulfate. The particles raised higher cancer risk of 1.62 × 10−6 by heavy metals (especially for Cd and As). This study provided detailed composition data and first comprehensive analysis of the aging processes of FW particles during the serious haze pollution period and their potential impact on human health.

Abstract. To understand the impact of fireworks burning (FW) particles on air quality and human health during winter haze period, thirty-nine elements, ten water-soluble ions and eight fractions of carbonaceous species in atmospheric PM2.5 at Nanjing were investigated during 2014 Chinese Spring Festival (SF). Serious regional haze pollution persisted throughout the entire sampling period, PM2.5 averaging at 113 ± 69 μg m−3 and visibility at 4.8 ± 3.2 km. The holiday effect led to almost all the chemical species decreasing during the SF, except for Al, K, Ba and Sr which were related to FW. The source contributions of coal combustion, vehicle emission and road dust descreased dramatically, whereas FW contributed to about half of the PM2.5 during SF period. The intensive emission of FW particles at New Year's Eve accounted for 60.1% of the PM2.5. They also significnatly modified the chemical compositions of PM2.5, with 39.3% contributed by increased organic matter, followed by steadly increased loadings of secondary inorganic ions. The aging processes of the FW particles lasted for at least six days reflected by the variation of SO42−, characterized by heterogeneous reactions of SO2 and NOx on crustal materials directly from FW, the replacement of Cl− by NO3− and SO42− coating of NO3− and SO42− on soot, formation of secondary organic aerosols and metal-catalyzed formation of NO3− and SO42− at higher relative humidity. During aging, the main contributors to the extinction coefficient shifted from elemental carbon and organic matter to sulfate ammonium. The particles raised higher cancer risks by heavy metals (especially for Cd and As) as 1.62 ×10−6. This study provided detailed composition data and first comprehensive analysis of the aging processes of FW particles at serious haze pollution period and their potential impact on human health.

To evaluate sampling artifacts of PM 2.5 with conventional filtration system (FS), a contrastive study between the FS and a honeycomb denuder system (HDS) in measuring atmospheric concentrations of PM 2.5 and its main water-soluble ions (Cl -, NO 3 -, SO 4 2-and NH 4 + ) was conducted at a urban site in Tianjin, China in both summer and winter. In this study, we confirmed the optimum concentration of absorbents of Na 2 CO 3 and citric acid for HDS were 3% and 6% in summer experiments and 4% and 5% in winter experiments. Daily mean concentrations of Cl -obtained by HDS were higher than those by FS both in summer and winter. In contrast, the HDS gave lower daily mean SO 4 2-concentrations than FS in both summer and winter. For NO 3 -and NH 4 + , concentrations obtained by HDS were lower than those obtained by FS in winter. However, the HDS gave larger values of NO 3 -and NH 4 + than FS in summer. The different results of different ions were in response to the concentrations of interfering gases in ambient air and chemical characteristics of ionic species. In addition, the concentrations of PM 2.5 obtained by HDS were higher than those obtained by FS in summer, while virtually no significant difference between HDS and FS in winter. Our study points out that investigating optimum concentrations of coating solutions before denuder system sampling is necessary. Moreover, it is essential to make careful evaluation and modification when applying FS in highly polluted Environment, especially for PM 2.5 ions determining.