Characteristics of water-soluble inorganic chemical components in size-resolved airborne particulate matters--Sheffield, UK.

To characterise the water-soluble inorganic components of PM(10) in the urban area of Sheffield, size-resolved aerosol samples were collected using an electric low pressure impactor (ELPI) during a 13-day sampling campaign in October and November 2006. Cl(-), NO(3)(-), SO(4)(2-), and NH(4)(+) were determined by ion chromatography, and Na(+), K(+), Mg(2+), and Ca(2+) by inductively coupled plasma-mass spectrometry. Back trajectories analyses revealed that the air masses could be classified into two main groups. In the "maritime regime", the air masses moved mostly over the sea and just short distances (ca. 100 to 150 km) over land; in the "terrestrial regime", the air masses had moved long distances (ca. 300 to 600 km) over land before reaching the sampling site. The chemical composition of the particles was strongly influenced by the origins of the air masses. Air mass belonging to the maritime regime brought more sea-salt species such as Na(+), Cl(-), and Mg(2+). Air mass belonging to the terrestrial regime carried more K(+) and secondary components like SO(4)(2-), NO(3)(-), and NH(4)(+). Sulfate showed bimodal distribution, peaking both in the fine mode (particle size <0.96 microm) and the coarse mode (particle size >0.96 microm). Nitrate exhibited a bimodal distribution in the terrestrial regime but only a coarse mode in maritime regime. Ammonium displayed a unimodal size distribution, peaking in the fine size range, mainly bound to sulfate and nitrate. In the maritime regime, chloride showed a unimodal distribution, peaking in the coarse size range. In the terrestrial regime, chloride appeared to be bimodal with one peak in the fine mode, reflecting the presence of chloride sources from industries, and another one in the coarse mode, mainly from sea spray. Although in general the air mass trajectories can be grouped into "maritime" and "terrestrial" regimes, the results suggest that air masses reaching Sheffield have been impacted by both maritime and terrestrial sources.

Heavy coal combustion as the dominant source of particulate pollution in Taiyuan, China, corroborated by high concentrations of arsenic and selenium in PM10.

Coal burning generates toxic elements, some of which are characteristic of coal combustion such as arsenic and selenium, besides conventional coal combustion products. Airborne particulate samples with aerodynamic diameter less than 10 microm (PM(10)) were collected in Taiyuan, China, and multi-element analyses were performed by inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS). Concentrations of arsenic and selenium from ambient air in Taiyuan (average 43 and 58 ng m(-3), respectively) were relatively high compared to what is reported elsewhere. Arsenic and selenium were found to be highly correlated (r=0.997), indicating an overwhelmingly dominant source. Correlation between these two chalcophile elements and the lithophile element Al is high (r is 0.75 and 0.72 for As and Se, respectively). This prompted the hypothesis that the particles were from coal combustion. The enrichment of the trace elements could be explained by the volatilization-condensation mechanism during coal combustion process. Even higher correlations of arsenic and selenium with PM(10) (r=0.90 and 0.88) give further support that airborne particulate pollution in Taiyuan is mainly a direct result of heavy coal consumption. This conclusion agrees with the results from our previous study of individual airborne particles in Taiyuan.