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PM2.5 (i.e., particles with aerodynamic diameters less than 2.5 μm) and the associated water-soluble, dissolved, and labile fractions of heavy metals (Cu, Pb, Mn, Ni, Co, Zn, Cr, and Cd) were determined in indoor air of twenty workplaces in Alexandroupolis (Northeastern Greece). PM2.5 concentrations exhibited significant variance across the workplaces ranging from 11.5 μg m−3 up to 276 μg m−3. The water-soluble metal concentrations varied between 0.67 ± 2.52 ng m−3 for Co and 27.8 ± 19.1 ng m−3 for Ni exhibiting large variations among the different workplaces. The water-soluble metal fractions were further treated to obtain the labile metal fraction (by binding with Chelex 100–chelating resin) that might represent a higher potential for bioaccessibility than the total water-soluble fraction. The largest labile (chelexed) fractions (48–67% of the corresponding water-soluble concentrations) were found for Cd, Mn, Cu, and Ni, while the labile fractions of Pb, Cr, Co, and Zn were relatively lower (34–42% of the corresponding water-soluble concentrations). Water-soluble and labile concentrations of heavy metals were further used to calculate cancer and non-cancer risks via inhalation of the PM2.5-bound metals. To our knowledge, this is the first study estimating the health risks due to the inhalation of water-soluble and labile metal fractions bound to indoor PM. [ABSTRACT FROM AUTHOR]

Featured Application: The deposition rate is a relevant and novel issue in air quality evaluation. Particularly, atmospheric micropollutant deposition rate measures represent a strategic element in environmental surveillance and in population exposure evaluation for POPs and metals. In recent years, studies on climate change have focused on reducing greenhouse gas emissions emitted by various civil and industrial processes. This study highlights the importance of characterizing the total deposition rates of airborne particles (bulk atmospheric deposition) in the surroundings of an industrial area along the north cost of the Lazio Region in Italy, to deepen knowledge about the potential impact of emissions from the coal-fired thermoelectric (CTE) power plant and other possible sources existing in the surrounding area. Four sampling sites were identified, and the monitoring plan was performed a yearlong with monthly collecting observation. The deposition samples were collected monthly and processed for determining organic (polychlorinated dibenzo-para-dioxins, PCDDs; polychlorinated dibenzofurans, PCDFs; dioxin-like polychlorinated biphenyls, DL-PCBs; polycyclic aromatic hydrocarbons, PAHs) and inorganic (metals) substances. The samples were collected monthly and sent for chemical characterization. In Europe and Italy, no reference values have been given for the deposition rates of chemicals, while some European countries have determined reference/guide values to which the authors will refer in this study. Therefore, the analytical results show that the deposition rates for PCDD/Fs and DL-PCBs are lower with respects guide values defined by Germany and Belgium; PAHs values are in line with those measured in other rural-type sites, while for metals the analytical results show a situation between rural and urban area. The approach used in this study can help to identify reference values for Italy in deposition rates, with the aim both to characterize the dynamic of pollution in area with multiple risk factors and to describe and protect human health from environmental exposures caused by the contamination of the food chain. [ABSTRACT FROM AUTHOR]

Nitro-monoaromatic hydrocarbons (NMAHs), such as nitrocatechols, nitrophenols and nitrosalicylic acids, are important constituents of atmospheric particulate matter (PM) water soluble organic carbon (WSOC) and humic-like substances (HULIS). Nitrated and oxygenated derivatives of polycyclic aromatic hydrocarbons (NPAHs, OPAHs) are toxic and ubiquitous in the ambient air; due to their light absorption properties, together with NMAHs they are part of aerosol brown carbon (BrC). We investigated the winter concentrations of these substance classes in size-resolved particulate matter (PM) from two urban sites in central and southern Europe, i.e. Mainz (MZ), Germany and Thessaloniki (TK), Greece. ∑11NMAH concentrations in PM10 and total PM were 0.51-8.38 and 12.1-72.1 ng m-3 at MZ and TK site, respectively, whereas ∑8OPAHs were 47-1636 and 858-4306 pg m-3, and ∑17NPAHs were ≤ 90 and 76-578 pg m-3, respectively. NMAHs and the water-soluble OPAHs contributed 0.4 and 1.8 %, and 0.0001 and 0.0002 % to the HULIS mass, at MZ and TK, respectively. The mass size distributions of the individual substances generally peaked in the smallest or second smallest size fraction i.e., < 0.49 μm or 0.49-0.95 μm. The mass median diameter (MMD) of NMAHs was 0.10 μm and 0.27 μm at MZ and TK, respectively, while the MMDs of NPAHs and OPAHs were both 0.06 μm at MZ, and 0.12 and 0.10 μm at TK. Correlation analysis between NMAHs, NPAHs and OPAHs from one side and WSOC, HULIS, nitrate, sulphate and potassium cation (K+) from another, suggested that the fresh biomass burning emissions dominated at the TK site, while aged air masses (influenced by biomass and fossil fuel burning) were predominant at the MZ site. [ABSTRACT FROM AUTHOR]

The Western Macedonian Lignite Center (WMLC) in northwestern Greece is the major lignite center in the Balkans feeding four major power plants of total power exceeding 4 GW. Concentrations of PM10 (i.e., particulate matters with diameters ≤10 μm) are the main concern in the region, and the high levels observed are often attributed to the activities related to power generation. In this study, the contribution of fugitive dust emissions from the opencast lignite mines to the ambient levels of PM10 in the surroundings was estimated by performing chemical mass balance (CMB) receptor modeling. For this purpose, PM10 samples were concurrently collected at four receptor sites located in the periphery of the mine area during the cold and the warm periods of the year (November-December 2011 and August-September 2012), and analyzed for a total of 26 macro- and trace elements and ionic species (sulfate, nitrate, chloride). The robotic chemical mass balance (RCMB) model was employed for source identification/apportionment of PM10 at each receptor site using as inputs the ambient concentrations and the chemical profiles of various sources including the major mine operations, the fly ash escaping the electrostatic filters of the power plants, and other primary and secondary sources. Mean measured PM10 concentrations at the different sites ranged from 38 to 72 μg m−3. The estimated total contribution of mines ranged between 9 and 22% in the cold period increasing to 36-42% in the dry warm period. Other significant sources were vehicular traffic, biomass burning, and secondary sulfate and nitrate aerosol. These results imply that more efficient measures to prevent and suppress fugitive dust emissions from the mines are needed. [ABSTRACT FROM AUTHOR]

The occurrence and atmospheric behavior of tri- to deca-polybrominated diphenyl ethers (PBDEs) were investigated during a 2-week campaign concurrently conducted in July 2012 at four background sites around the Aegean Sea. The study focused on the gas/particle (G/P) partitioning at three sites (Ag. Paraskevi/central Greece/suburban, Finokalia/southern Greece/remote coastal, and Urla/Turkey/rural coastal) and on the size distribution at two sites (Neochorouda/northern Greece/rural inland and Finokalia/southern Greece/remote coastal). The lowest mean total (G + P) concentrations of ∑PBDE (BDE-28, BDE-47, BDE-66, BDE-99, BDE-100, BDE-153, BDE-154) and BDE-209 (0.81 and 0.95 pg m, respectively) were found at the remote site Finokalia. Partitioning coefficients, K , were calculated, and their linear relationships with ambient temperature and the physicochemical properties of the analyzed PBDE congeners, i.e., the subcooled liquid pressure ( P °) and the octanol-air partition coefficient ( K ), were investigated. The equilibrium adsorption ( P °-based) and absorption ( K -based) models, as well as a steady-state absorption model including an equilibrium and a non-equilibrium term, both being functions of log K , were used to predict the fraction Φ of PBDEs associated with the particle phase. The steady-state model proved to be superior to predict G/P partitioning of BDE-209. The distribution of particle-bound PBDEs across size fractions < 0.95, 0.95-1.5, 1.5-3.0, 3.0-7.2, and > 7.2 μm indicated a positive correlation between the mass median aerodynamic diameter and log P ° for the less brominated congeners, whereas a negative correlation was observed for the high brominated congeners. The potential source regions of PBDEs were acknowledged as a combination of long-range transport with short-distance sources. [ABSTRACT FROM AUTHOR]

In this study, we report for the first time particle number doses in different parts of the human respiratory tract and real-time deposition rates for particles in the 10 nm to 10 μm size range emitted by digital printing operations. Particle number concentrations (PNCs) and size distribution were measured in a typical small-sized printing house using a NanoScan scanning mobility particle sizer and an optical particle sizer. Particle doses in human lung were estimated applying a multiple-path particle dosimetry model under two different breathing scenarios. PNC was dominated by the ultrafine particle fractions (UFPs, i.e., particles smaller than 100 nm) exhibiting almost nine times higher levels in comparison to the background values. The average deposition rate fοr each scenario in the whole lung was estimated at 2.0 and 2.9 × 10 particles min, while the respective highest particle dose in the tracheobronchial tree (2.0 and 2.9 × 10 particles) was found for diameter of 50 nm. The majority of particles appeared to deposit in the acinar region and most of them were in the UFP size range. For both scenarios, the maximum deposition density (9.5 × 10 and 1.5 × 10 particles cm) was observed at the lobar bronchi. Overall, the differences in the estimated particle doses between the two scenarios were 30-40% for both size ranges. [ABSTRACT FROM AUTHOR]

Thirteen particle-phase PAHs, including nine >4-ring congeners [Benz[a]anthracene (BaAn), Chrysene (Chry), Benzo[b]fluoranthene (BbF), Benzo[k]fluoranthene (BkF), Benzo[e]pyrene (BeP), Benzo[a]pyrene (BaP), Dibenzo[a,h]anthracene (dBaAn), Benzo[g,h,i]perylene (BghiPe), Indeno(1,2,3-c,d)pyrene (IP)], listed by IARC (International Agency for Research on Cancer) as class 1, class 2A, and 2B carcinogens, plus four ≤4-ring congeners [Phenanthrene (Ph), Anthracene (An), Fluoranthene (Fl), Pyrene (Py)], were concurrently measured in inhalable and respirable particle fractions (PM and PM) at a heavy-traffic and an urban background site in Thessaloniki, northern Greece, during the warm and the cold period of the year. Carcinogenic and mutagenic potencies of the PAH-bearing particles were calculated, and the inhalation cancer risk (ICR) for local population was estimated. Finally, Chemical Mass Balance (CMB) modeling was employed for the source apportionment of ambient PAH levels and the estimated lung cancer risk. Resulted inhalation cancer risk during winter was found to be equivalent in the city center and the urban background area suggesting that residential wood burning may offset the benefits from minor traffic emissions. [ABSTRACT FROM AUTHOR]