The impact of seasonal varied human activity on characteristics and sources of heavy metals in metropolitan road dusts.

. Knowledge of aerosol chemistry in densely populated regions is critical for effective reduction of air pollution, while such studies have not been conducted in Changzhou, an important manufacturing base and populated city in the Yangtze River Delta (YRD), China. This work, for the first time, performed a thorough chemical characterization on the fine particulate matter (PM2.5) samples, collected during July 2015 to April 2016 across four seasons in this city. A suite of analytical techniques was employed to measure the organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), water-soluble inorganic ions (WSIIs), trace elements, and polycyclic aromatic hydrocarbons (PAHs) in PM2.5; in particular, an Aerodyne soot particle aerosol mass spectrometer (SP-AMS) was deployed to probe the chemical properties of water-soluble organic aerosol (WSOA). The average PM2.5 concentration was found to be 108.3 µg m−3, and all identified species were able to reconstruct ∼ 80 % of the PM2.5 mass. The WSIIs occupied about half of the PM2.5 mass (∼ 52.1 %), with SO42−, NO3−, and NH4+ as the major ions. On average, nitrate concentrations dominated over sulfate (mass ratio of 1.21), indicating that traffic emissions were more important than stationary sources. OC and EC correlated well with each other and the highest OC ∕ EC ratio (5.16) occurred in winter, suggesting complex OC sources likely including both secondary and primary ones. Concentrations of eight trace elements (Mn, Zn, Al, B, Cr, Cu, Fe, Pb) can contribute up to ∼ 5.0 % of PM2.5 during winter. PAH concentrations were also high in winter (140.25 ng m−3), which were predominated by median/high molecular weight PAHs with five and six rings. The organic matter including both water-soluble and water-insoluble species occupied ∼ 21.5 % of the PM2.5 mass. SP-AMS determined that the WSOA had average atomic oxygen-to-carbon (O ∕ C), hydrogen-to-carbon (H ∕ C), nitrogen-to-carbon (N ∕ C), and organic matter-to-organic carbon (OM ∕ OC) ratios of 0.54, 1.69, 0.11, and 1.99, respectively. Source apportionment of WSOA further identified two secondary OA (SOA) factors (a less oxidized and a more oxidized oxygenated OA) and two primary OA (POA) factors (a nitrogen-enriched hydrocarbon-like traffic OA and a local primary OA likely including species from cooking, coal combustion, etc.). On average, the POA contribution outweighed SOA (55 % vs. 45 %), indicating the important role of local anthropogenic emissions in the aerosol pollution in Changzhou. Our measurement also shows the abundance of organic nitrogen species in WSOA, and the source analyses suggest these species are likely associated with traffic emissions, which warrants more investigations on PM samples from other locations.

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Chemical characterization of fine particulate matter in Changzhou, China, and source apportionment with offline aerosol mass spectrometry

Aerosol characteristics and sources in Yangzhou, China resolved by offline aerosol mass spectrometry and other techniques

Characteristics, sources and health risks of toxic species (PCDD/Fs, PAHs and heavy metals) in PM2.5 during fall and winter in an industrial area

Relationship between domestic smoking and metals and rare earth elements concentration in indoor PM2.5.

In this work, the seasonal variations and sources of trace metal elements in atmospheric fine aerosols (PM2.5) were investigated for a year-long field campaign from July 2012 to June 2013, conducted in suburban Nanjing, eastern China, at a site adjacent to an industry zone. The PM2.5 samples collected across four seasons were analyzed for 17 metal elements, namely, Sodium (Na), Magnesium (Mg), Aluminum (Al), Vanadium (V), Chromium (Cr), Manganese (Mn), Nickel (Ni), Copper (Cu), Zinc (Zn), Arsenic (As), Selenium (Se), Strontium (Sr), Cadmium (Cd), Barium (Ba), Lead (Pb), Molybdenum (Mo), and Antimony (Sb) using an inductively coupled plasma mass spectrometry (ICP-MS). We found that the total concentration of all 17 metal elements was 1.23 μg/m3, on average accounting for 1.0% of the total PM2.5 mass. For our data, mass concentrations of Al, Cd, Ba were highest in summer, Mg, Cu, Zn, Se, Pb peaked in autumn, Cr, Mn, Ni, As, Sr, Sb increased significantly in winter, while the concentrations of Na, V, Mo were at their highest levels in spring. Air mass back trajectory analysis suggested that air parcels that arrived at the site originated from four dominant regions (Japan, yellow sea and bohai; Southeast of China, the Pacific Ocean; Southwest of Jiangsu and Anhui province; Northern Asia inland and Mongolia region), in particular, the one from Northern Asia inland and Mongolia contained the highest concentrations of As, Sb, Sr, and was predominant in winter. Positive matrix factorization (PMF) analyses revealed that the industrial emission is the largest contributor (34%) of the observed metal elements, followed by traffic (25%), soil dust (19%), coal combustion (10%), incineration of electronic waste (9%), and a minor unknown source (3%). In addition, we have also investigated the morphology and composition of particles by using the scanning electron microscopy (SEM)/energy-dispersive spectrometry (EDS) techniques, and identified particles from coal burning sources, etc., similar to the PMF results.

https://www.mdpi.com/2073-4433/7/12/153/pdf

Bingfang Guo

Papers

Seasonal Variations and Sources of 17 Aerosol Metal Elements in Suburban Nanjing, China