Gaseous Polycyclic Aromatic Hydrocarbons Concentrations Research Articles

Net volatilization of PAHs from the North Pacific to the Arctic Ocean observed by passive sampling.

The North Pacific-Arctic Oceans are important compartments for semi-volatile organic compounds' (SVOCs) global marine inventory, but whether they act as a "source" or "sink" remains controversial. To study the air-sea exchange and fate of SVOCs during their poleward long-range transport, low-altitude atmosphere and surface seawater were measured for polycyclic aromatic hydrocarbons (PAHs) by passive sampling from July to September in 2014. Gaseous PAH concentrations (0.67-13ngm-3) were dominated by phenanthrene (Phe) and fluorene (Flu), which displayed an inverse correlation with latitude, as well as a significant linear relationship with partial pressure and inverse temperature. Concentrations of PAHs in seawater (1.8-16ngL-1) showed regional characteristics, with higher levels near the East Asia and lower values in the Bering Strait. The potential impact from the East Asian monsoon was suggested for gaseous PAHs, which - similar to PAHs in surface seawater - were derived from combustion sources. In addition, the data implied net volatilization of PAHs from seawater into the air along the entire cruise; fluxes displayed a similar pattern to regional and monthly distribution of PAHs in seawater. Our results further emphasized that air-sea exchange is an important process for PAHs in the open marine environments.

Polycyclic Aromatic Hydrocarbon Gaseous Emissions from Household Cooking Devices: A Kenyan Case Study.

In developing countries, household energy use is highly variable and complex, yet emissions arising from fuel combustion indoors are typically poorly quantified. Polycyclic aromatic hydrocarbons (PAHs) are emitted during the combustion of organic fuels such as charcoal and biomass. In the present study, multichannel polydimethylsiloxane rubber traps were used for gas-phase PAH sampling and extracted using a low-solvent volume plunger-assisted solvent extraction method. Sixteen US Environmental Protection Agency priority PAHs, primarily in the gas phase, were investigated in indoor air of rural and urban residential homes in coastal Kenya (Mombasa and Taita Taveta Counties) using typical combustion devices of each area. Average gaseous PAH concentrations per household were higher in rural (ranging 0.81-6.09 µg m-3 ) compared to urban (ranging 0-2.59 µg m-3 ) homes, although ambient PAH concentrations were higher in urban environments, likely attributable to traffic contributions. The impact of fuel choice and thereby combustion device on PAH emissions was very clear, with the highest concentrations of PAHs quantified from wood-burning emissions from 3-stone stoves (total PAH averages 46.23 ± 3.24 µg m-3 [n = 6]). Average benzo[a]pyrene equivalent total concentrations were evaluated for the priority PAHs and ranged from not detected to 43.31, 88.38, 309.61, and 453.88 ng m-3 for gas, kerosene, jiko, 3-stone, and improved 3-stone stoves, respectively. Environ Toxicol Chem 2020;39:538-547. © 2019 SETAC.

Spatiotemporal distribution and dynamic modeling of atmospheric gaseous polycyclic aromatic hydrocarbons in a rapidly urbanizing city: Nanjing, China.

Multiple studies have evaluated the concentration and lung cancer risk of polycyclic aromatic hydrocarbons (PAHs). However, the monitoring and dynamic modeling of PAHs with a high resolution were relatively insufficient. We investigated the spatiotemporal distribution of gaseous PAH concentrations using passive air samplers with high sampling density in an industrial city of Nanjing, China (January and October 2015) and found that the gaseous PAH concentrations in western Nanjing were higher than those in eastern Nanjing, mainly because of emission source distribution and wind action. There were notable seasonal changes in PAH concentrations: winter > autumn > spring > summer. We developed an atmospheric PAH dynamic model with a high resolution of 1km2 based on the advection-diffusion equation and coupled with an emissions inventory and atmospheric transportation processes. Acenaphthene was selected as a proxy for gaseous PAHs. The modeled acenaphthene concentrations were similar to the concentrations measured. Moreover, we used the model to identify the impact of meteorological factors on gaseous PAHs via scenario analysis and found that a narrow-range temperature change and even heavy rainfall may not significantly affect atmospheric gaseous PAH concentrations, whereas the wind played an important part in transferring PAHs and changing their geographic distribution.

Assessment of airborne polycyclic aromatic hydrocarbons in a megacity of South China: Spatiotemporal variability, indoor-outdoor interplay and potential human health risk

Although a number of studies have assessed the occurrence of atmospheric polycyclic aromatic hydrocarbons (PAHs) in indoor environment, few studies have systemically examined the indoor-outdoor interplay of size-dependent particulate PAHs and potential health risk based on daily lifestyles. In the present study, size-dependent particle and gaseous samples were collected both indoors and outdoors within selected schools, offices and residences located in three districts of Guangzhou, China with different urbanization levels during the dry and wet weather seasons. Results from measurements of PAHs showed that higher total PAH concentrations occurred in residential areas than in other settings and in indoor than in outdoor environments. Compositional profiles and size distribution patterns of particle-bound PAHs were similar indoors and outdoors, predominated by 4-and 5-ring PAHs and the 0.56–1.0 μm particle fraction. Statistical analyses indicated that outdoor sources may have contributed to 38–99% and 62–100% of the variations for indoor particle-bound and gaseous PAH concentrations, respectively. Incremental life cancer risk (ILCR) from human exposure to indoor and outdoor PAHs based on different lifestyles followed the order of adults > children > adolescents > seniors. All average ILCR values for four age groups were below the lower limit of the Safe Acceptable Range (10−6). In addition, the ILCR value for adults (average: 7.2 × 10−7; 95% CI: 5.4 × 10−8‒2.5 × 10−6), estimated from outdoor air PAH levels with 24-h exposure time, was significantly higher than our assessment results (average: 5.9 × 10−7; 95% CI: 6.3 × 10−8‒1.9 × 10−6), suggesting the significance of assessing human inhalation exposure risks of indoor and outdoor PAHs in urban air based on daily lifestyles.

Use of a numerical simulation approach to improve the estimation of air-water exchange fluxes of polycyclic aromatic hydrocarbons in a coastal zone

The air-water exchange is important for determining the transport, fate, and chemical loading of polycyclic aromatic hydrocarbons (PAHs) in the atmosphere and in aquatic systems. Investigations of PAH air-water exchange are mostly based on observational data obtained using complicated field sampling processes. This study proposes a new approach to improve the estimation of long-term PAH air-water exchange fluxes by using a multivariate regression model to simulate hourly gaseous PAH concentrations. Model performance analysis and the benefits from this approach indicate its effectiveness at improving the flux estimations and at decreasing the field sampling difficulty.The proposed GIS mapping approach is useful for box model establishment and is tested for visualization of the spatiotemporal variations of air-water exchange fluxes in a coastal zone. The air-water exchange fluxes illustrated by contour maps suggest that the atmospheric PAHs might have greater impacts on offshore sites than on the coastal area in this study.

Gaseous polycyclic aromatic hydrocarbon concentrations are higher in urban forests than adjacent open areas during summer but not in winter – Exploratory study

While the potential of plants to uptake polycyclic aromatic hydrocarbons (PAHs) is widely acknowledged, empirical evidence of the effects of this process on local atmospheric PAH concentrations and human health is tenuous. We measured gaseous PAH concentrations using passive samplers in urban tree-covered areas and adjacent open, treeless areas in a near-road environment in Finland to gain information on the ability of urban vegetation to improve air quality. The ability of urban, mostly deciduous, vegetation to affect PAHs was season dependent: during summer, concentrations were significantly higher in tree-covered areas, while in the fall, concentrations in open areas exceeded those in tree-covered areas. During winter, concentrations in tree-covered areas were either lower or did not differ from those in open areas. Results of this study imply that the commonly believed notion that trees unequivocally improve air quality does not apply to PAHs studied here.

Emission of polycyclic aromatic hydrocarbons from different types of motor vehicles’ exhaust

In this study, most toxic polycyclic aromatic hydrocarbons (PAHs) in the vehicle exhaust were characterized and quantified carried on a chassis dynamometer test. The vehicle exhaust samples were collected under different driving cycles of vehicles such as acceleration, deceleration, uniform speed and idle conditions. The results show that the concentration of lower molecular weight PAHs (2–3 rings) in gaseous phase was higher than that in solid phase, while the concentration of high molecular weight PAHs (5–6 rings) was abundant in solid phase. The sum of two-ring, three-ring and four-ring PAHs accounted for ~87 % of the total gaseous PAH concentrations, while about 10 and 4 % of gaseous-phase PAHs were five rings and six rings, respectively. By comparison, the percentage of two-ring and three-ring PAHs were decreased in the solid-phase PAHs. Three-, four-, and five-ring PAHs had an absolute advantage in solid phase, which accounted for 89 and 81 % of the total PAHs in diesel and gasoline vehicle exhaust, respectively. The Benzo(a)pyrene-equivalent carcinogenic power (BaPE) value of PAHs ranged from 0.558 to 5.684 μg m−3 in vehicle exhaust, and the ratio of BaPE·BaP−1 was between 2.029 and 8.413. In other words, the PAHs contributed 102.9–741.3 % of the BaP equivalent carcinogenic toxicity except for sole BaP.

Significance of population centers as sources of gaseous and dissolved PAHs in the lower Great Lakes.

Polyethylene passive samplers (PEs) were used to measure concentrations of gaseous and dissolved polycyclic aromatic hydrocarbons (PAHs) in the air and water throughout the lower Great Lakes during summer and fall of 2011. Atmospheric Σ15PAH concentrations ranged from 2.1 ng/m3 in Cape Vincent (NY) to 76.4 ng/m3 in downtown Cleveland (OH). Aqueous Σ18PAH concentrations ranged from 2.4 ng/L at an offshore Lake Erie site to 30.4 ng/L in Sheffield Lake (OH). Gaseous PAH concentrations correlated strongly with population within 3-40 km of the sampling site depending on the compound considered, suggesting that urban centers are a primary source of gaseous PAHs (except retene) in the lower Great Lakes region. The significance of distant population (within 20 km) versus local population (within 3 km) increased with subcooled liquid vapor pressure. Most dissolved aqueous PAHs did not correlate significantly with population, nor were they consistently related to river discharge, wastewater effluents, or precipitation. Air-water exchange calculations implied that diffusive exchange was a source of phenanthrene to surface waters, while acenaphthylene volatilized out of the lakes. Comparison of air-water fluxes with temperature suggested that the significance of urban centers as sources of dissolved PAHs via diffusive exchange may decrease in warmer months.

Spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of Xiamen, China

An intensive sampling program was conducted from October 2008 to September 2009 at the five different environmental sites in Xiamen, Fujian Province, to study the spatial and temporal characteristics of Polycyclic Aromatic Hydrocarbons (PAHs) in the gaseous and particulate phase, respectively. The PAHs concentrations at different sites were quite distinct during four seasons. The average concentrations of PAHs in winter were about 8.4 times higher than those in spring, and the concentrations of background were 0.56 times lower than those of industrial area. In addition, the higher temperature in summer affected the particle/gas partitioning of PAHs and led to the higher concentrations of gaseous PAHs. Diagnostic ratios of PAHs, which were employed to indicate the primary sources of PAHs in Xiamen, showed that the traffic vehicle exhaust was the largest contributor and the primary source for PAHs in Xiamen, especially in urban area; while the stationary combustion processes, such as petrochemical factories and power plants, were mainly responsible for PAHs sources in the industrial areas. The health risk of PAHs in the particulate phase was higher than those of the gaseous phase at the five sampling sites. The average toxic equivalent (BaPeq) of the benzo[a]pyrene values for PAHs were 0.14, 0.32, 1.38 and 3.59ngm−3 in spring, summer, autumn and winter, respectively. Furthermore, the results of average BaPeq in all four seasons indicated that the health risks of particulate PAHs were higher than those of the gaseous PAHs at different sampling sites.

Gas–particle concentrations of atmospheric polycyclic aromatic hydrocarbons at an urban and a residential site in Osaka, Japan: Effect of the formation of atmospherically stable layer on their temporal change

A comparative study on atmospheric polycyclic aromatic hydrocarbons (PAHs) in particulate matter and the gaseous phase was performed at an urban and a residential site in Osaka, Japan, during 2005–2006. PAH concentrations at the urban site were found to be approximately twice higher than those at the residential site. At both sites, particulate PAH concentrations increased mainly in winter while the trends of temporal change in gaseous PAH concentrations were not clearly observed. The main sources of PAHs were estimated to be local traffic, e.g., diesel engines with catalytic converter. PAH concentrations did not significantly negatively correlate with ozone concentrations and meteorological parameters. Gas–particle partitioning coefficients of representative PAHs with low molecular weight (LMW) significantly negatively correlated with ambient temperature, showing that temporal change in the LMW PAH concentrations in PM could be attributable to the shift of their gas–particle distribution caused by the change in ambient temperature. For the first time, we studied the effect of the formation of atmospherically stable layer following an increase in PAH concentrations in Japan. At the urban site, PAHs showed a significant positive correlation with potential temperature gradients, indicating that temporal variability in PAH concentrations would be dominantly controlled by the formation of atmospherically stable layer in Osaka area.

Customers' exposure to PM2.5 and polycyclic aromatic hydrocarbons in smoking/nonsmoking sections of 24-h coffee shops in Taiwan

In Taiwan 24-h coffee shops have become popular gathering areas for young people. This study assesses customers' exposures to PM(2.5) and gaseous/particulate polycyclic aromatic hydrocarbons (PAHs) in such an environment. Potential influential factors were also evaluated. Two coffee shops with different types of smoking/nonsmoking divisions were selected. Sampling was conducted from 1300 to 2100 hours on Saturdays and Sundays during December 2000 and January 2001. Personal environmental monitors mounted with Teflon filters and polyurethane foams were used for particulate and gaseous sampling. PAHs were analyzed with GC-FID. Principal component analysis was used to explore the differences in the patterns of gaseous and particulate PAHs. Stepwise regression analysis was used to evaluate the contribution of various factors. The geometric mean (GM) of PM(2.5), particulate and gaseous PAH exposures were 83.7, 0.46 and 1.01 microg/m(3), respectively. Their exposure concentrations were about two to five times those of residential indoor environments in Taiwan. Smoking and vehicle exhaust were two major exposure sources. The gaseous PAH concentrations in the two sections of both shops were significantly correlated. The divisions between smoking and nonsmoking sections in neither of the coffee shops were effective to prevent dispersion of gaseous pollutants. In both shops, the concentrations of PM(2.5) and associated PAHs, respectively, were about 22-28 microg/m(3) and 0.07 microg/m(3) higher in smoking areas compared to nonsmoking areas. It was also found that each additional cigarette resulted in a 0.22-0.42 microg/m(3) PM(2.5) incremental increase in nonsmoking customers' exposure in the smoking section.

Simultaneous Liquid Chromatographic Determination of 39 Polycyclic Aromatic Hydrocarbons in Indoor and Outdoor Air and Application to a Survey on Indoor Air Pollution in Fuji, Japan

An analytical method was established for the simultaneous determination of 39 polycyclic aromatic hydrocarbons (PAHs) in air. The method was applied to a survey of gaseous and particulate PAHs in household indoor air. The survey was performed in 21 houses in the summer of 1999 and in 20 houses in the winter of 1999-2000 in Fuji, Japan. Thirty-eight PAHs were determined in indoor and outdoor air in the summer, and 39 PAHs were determined in indoor and outdoor air in the winter. The concentrations of gaseous PAHs in indoor air tended to be higher than those in outdoor air in the summer and winter. The concentrations of particulate PAHs in indoor air were the same as or lower than those in outdoor air in the summer and winter. PAH profiles, correlations between PAH concentrations, and multiple regression analysis were used to determine the factors affecting the indoor PAH concentrations. These results showed that gaseous PAHs in indoor air were primarily from indoor emission sources, especially during the summer, and that indoor particulate PAH concentrations were significantly influenced by outdoor air pollution.

Diffusive Exchange of Polycyclic Aromatic Hydrocarbons across the Air−Water Interface of the Patapsco River, an Urbanized Subestuary of the Chesapeake Bay

Air−water exchange fluxes of 13 polycyclic aromatic hydrocarbons (PAHs) were determined along a transect in the Patapsco River from the Inner Harbor of Baltimore, MD, to the mainstem of the northern Chesapeake Bay. Sampling took place at six sites during three sampling intensives (June 1996, February 1997, and July 1997) and at one site every ninth day between March 1997 and March 1998 to measure spatial, daily, and annual variability in the fluxes. The direction and magnitude of the daily fluxes of individual PAHs were strongly influenced by the wind speed and direction, by the air temperature, and by the highly variable PAH concentrations in the gas and dissolved phases. Individual fluxes ranged from 14 200 ng m-2 day-1 net volatilization of fluorene during high winds to 11 400 ng m-2 day-1 net absorption of phenanthrene when prevailing winds blowing from the northwest across the city of Baltimore elevated gaseous PAH concentrations over the water. The largest PAH volatilization fluxes occurred adjacent...