Seasonal variation, sources and gas/particle partitioning of polycyclic aromatic hydrocarbons in Guangzhou, China

Air samples were collected weekly at an urban site and a suburban site in Guangzhou City, China, from April 2005 to March 2006, to measure the concentrations of polycyclic aromatic hydrocarbons (PAHs) in the ambient air and study their seasonal variations, gas/particle partitioning, origins and sources. The concentrations of ∑ 16-PAHs (particle + gas) were 129.9 ± 73.1 ng m⁻³ at the urban site and 120.4 ± 48.5 ng m⁻³ at the suburban site, respectively. It was found that there was no significant difference in PAH concentrations between the urban and suburban sites. Seasonal variations of PAH concentrations at the two sampling sites were similar, with higher levels in the winter that gradually decreased to the lowest levels in the summer. The average concentrations of ∑ 16-PAHs in the winter samples were approximately three times higher than those of the summer samples because in the summer local emissions dominated, and in the winter the contribution from outside sources or transported PAHs is increased. The plot of logK_p versus logP_L⁰ for the data sets of summer and winter season samples had significantly different slopes at both sampling sites. The slopes for the winter samples were steeper than those for the summer samples. It was also observed that gas/particle partitioning of PAHs showed different characteristics depending on air parcel trajectories. Steeper slopes were obtained for an air parcel that traveled across the continent to the sampling site from the northern or northeastern sector, whereas shallower slopes were obtained for air masses that traveled across the sea from the southern or eastern sector. Diagnostic ratio analytical results imply that the origins of PAHs were mainly from petroleum combustion and coal/biomass burning. The anthracene/phenanthrene and benzo[a]anthracene/chrysene ratios in the winter were significantly lower than those in the summer, which indicate that there might be long-range transported PAH input to Guangzhou in the winter.     

Gas-particle partitioning of polychlorinated naphthalenes and non- and mono-ortho-substituted polychlorinated biphenyls in arctic air

Gas-particle partitioning relationships were developed for partitioning of polychlorinated naphthalenes (PCNs) and non- and mono-ortho PCBs in arctic air by regressing observed gas-particle partition coefficients, K(P), at Alert and Dunai in the high Arctic with temperature-adjusted experimental vapor pressures (p(L) degrees ) and octanol-air partition coefficients (K(OA)). Slopes were near -0.5 and 0.5 for log p(L) degrees and log K(OA), respectively, at both sites, indicating that aerosol characteristics and partitioning processes were similar at the two sites. The K(OA) absorption model provided an adequate estimate of the percentage of PCNs and non-/mono-ortho PCBs associated with particulate matter, based on fraction of organic matter (f(OM)) ranging from 0.074 to 0.12, compared to the Junge-Pankow adsorption model, which slightly over-estimated the distribution on particles. There were no indications that partitioning to soot carbon influences the observed gas-particle distribution for PCNs and non-/mono-ortho PCBs in arctic air as has been observed for PAHs in recent studies at temperate locations.     

Characterization, identification of ambient air and road dust polycyclic aromatic hydrocarbons in central Taiwan, Taichung

The concentrations of ambient air polycyclic aromatic hydrocarbons (PAHs) were measured simultaneously in an industrial area (Taichung Industrial Park, TIP) and suburban area (Tunghai University, THU) in central Taiwan, Taichung. A total of samples were collected simultaneously at the two sites between August 2002 and March 2003. Particle-bound PAHs (p-PAHs) were collected on quartz filters and gas-phase PAHs (g-PAHs) on glass cartridges using polyurethane foam sampler, respectively. Both types of samples were extracted with dichloromethane/n-hexane mixture (50/50, v/v) for 24 h, then the extracts were subjected to gas chromatography/mass spectrometric analysis. Moreover, the roadside dust particle PAHs composition were also collected and analyzed at TIP, THU and traffic road sampling sites. The five main road lines in Taichung City were selected as traffic road sampling sites. Correlation studies between PAHs concentrations and meteorological parameters were revealed that temperature has greater effects (P>0.6) than other meteorological parameters such as wind speed, relative humidity and atmospheric pressure on g-PAHs and p-PAHs. PAHs sources were resolved by using principal component analysis and diagnostic ratios. The major sources of PAHs were combustion, traffic vehicle exhaust (diesel and gasoline engine), incinerator and industrial stationary sources at both sampling sites in central Taiwan.     

Gas/particle partitioning of seven volatile polycyclic aromatic hydrocarbons in a heavy traffic urban area

Air samples (vapor- and particle-phase) were taken for 19 sampling events during the period from December 1997 to July 1998 in an urban site in the center of Athens. The urban site is densely populated and characterized by heavy traffic circulation and elevated concentrations of VOCs, NO(x), CO and smoke. Seven volatile polycyclic aromatic hydrocarbons (PAHs) were determined in samples. The temperature dependence of gas-phase atmospheric concentration of PAHs, C(g), was investigated using diagrams of natural logarithm of partial pressures (lnP) vs. reciprocal mid-point temperatures. For the six of seven volatile PAHs, the temperature dependence of lnP was statistically significant (at least at the 90% confidence level) and the temperature accounted for 21-67% of the variability in gas-phase concentrations. The gas-phase concentration C(g) of the very volatile PAHs was affected more significantly by changes in temperature, but the variation of the less-volatile PAHs fluoranthene and pyrene C(g), was better explained by changes in temperature. The temperature dependence of gas/particle partitioning constant K(P) was also examined. Regressions of log(K(P))(-1) vs. T(-1) for fluorene, fluoranthene and pyrene were classified into two different temperature ranges. The gas/particle partitioning of PAHs was studied by correlating the partition constant to the sub-cooled liquid saturation vapor pressure (P(L)(o)). The Junge adsorption model underestimated the particle fraction of volatile PAHs probably due to the presence of non-exchangeable fraction. Slopes (m(r)) of the regressions logK(P) vs. logP(L)(o) were different from the value -1 as Pankow's theory predicts. The short distance between the sampling point and the emission sources is also estimated to be a factor that causes deviations from the theoretical value. Evidence that atmospheric conditions favorable for secondary aerosol formation coincide with higher value of m(r), was provided by limited sampling events. An interrelation was found to exist between the m(r) values, allowing the prediction of the gas/particle partitioning of a series of seven PAHs by the measurement of a single PAH partitioning.     

Sources of polycyclic aromatic hydrocarbons (PAHs) in street dust in a tropical Asian mega-city, Bangkok, Thailand

We collected samples of roadside air, automobile exhaust soot, tires, asphalt, and used engine oil in a tropical Asian mega-city, Bangkok, Thailand, and analyzed them for polycyclic aromatic hydrocarbons (PAHs) and hopanes. The concentrations and compositions of PAHs and hopanes were utilized to identify the sources of PAHs in street dust, in which high concentrations of PAHs were reported in our previous study. Weight-based concentrations of total PAHs had the following order: gasoline-powered vehicle soot (2600+/-2900 microg/g; n=4)>diesel-powered vehicle soot (115+/-245 microg/g; n=7) approximately roadside aerosols (101+/-35 microg/g; n=5) approximately used engine oil (97+/-65 microg/g; n=4) approximately tire wear particles (82+/-41 microg/g; n=5)>asphalt (2.3+/-1.6 microg/g; n=3)>street dust (1.1+/-0.8 microg/g; n=10). In cluster analysis, all the source materials fell into different clusters from that in which street dust fell, indicating that multiple source materials contribute to PAHs in the street dust. Multiple regression analysis of PAH profiles and diagnostics of hopane compositions identified tire debris as the major contributor of PAHs to street dust, followed by diesel vehicle exhaust.     

Ambient volatile organic compound (VOC) concentrations around a petrochemical complex and a petroleum refinery

Air samples were collected between September 2000 and September 2001 in Izmir, Turkey at three sampling sites located around a petrochemical complex and an oil refinery to measure ambient volatile organic compound (VOC) concentrations. VOC concentrations were 4-20-fold higher than those measured at a suburban site in Izmir, Turkey. Ethylene dichloride, a leaded gasoline additive used in petroleum refining and an intermediate product of the vinyl chloride process in the petrochemical complex, was the most abundant volatile organic compound, followed by ethyl alcohol and acetone. Evaluations based on wind direction clearly indicated that ambient VOC concentrations measured were affected by the refinery and petrochemical complex emissions. VOC concentrations showed seasonal variations at all sampling sites. Concentrations were highest in summer, followed by autumn, probably due to increased evaporation of VOCs from fugitive sources as a result of higher temperatures. VOC concentrations generally increased with temperature and wind speed. Temperature and wind speed together explained 1-60% of the variability in VOC concentrations. The variability in ambient VOC concentrations that could not be explained by temperature and wind speed can be attributed to the effect of other factors (i.e. wind direction, other VOC sources).     

A sensitivity analysis on the atmospheric transformation and deposition of mercury in north-eastern USA

This paper presents the results of a sensitivity analysis on the factors that affect dry and wet deposition of atmospheric mercury (Hg), using a regional scale air quality model. Simulations were conducted for the north-eastern USA during a summer week and a winter week in 1997. Simulation results for the summer week and the winter week in general showed similar responses to changes in emission, environmental conditions, and alternative chemical mechanisms. Reduction of the ambient concentrations of soot or ozone was shown to reduce the wet deposition of Hg. When averaged over the summer and the winter week, the total deposition to the simulation domain would be reduced by 26% by reducing Hg emission from anthropogenic sources within the domain by 50%. For individual grids, however, only locations near local sources obtained noticeable reductions in ambient concentration and wet deposition due to the influence of re-emission from the natural surfaces and regional/global scale transport. The reduction in deposition would reach 36% if all Hg(II) emitted from anthropogenic sources were attached to particles. The total deposition was predicted to decrease by 22% when the gas phase Hg(II)-Hg(p) partitioning was included in the model. Only small changes in total deposition were observed by including the gas-phase ozone-Hg(0), reaction and the aqueous phase chlorine-Hg(0), reaction, and by lowering ambient concentrations of Hg(II) and Hg(p) at the upper lateral boundaries. During the summer week, Hg(II) deposition contributed 40% or more to the total deposition. The contribution increased to 70% in the winter week.     

Inhalation exposure of traffic police officers to polycyclic aromatic hydrocarbons (PAHs) during the winter in Beijing, China

This study concerns the use of personal samplers to evaluate the exposure of traffic police to polycyclic aromatic hydrocarbons (PAHs) during the winter of 2005 in Beijing. We measured the samples collected for gas and particulate phases PAHs with the same technique used for an earlier study during the summer of 2004, and evaluated exposure risk based on the calculated benzo(a)pyrene equivalent concentrations (BaP(eq)) of both summer and winter. The mean exposure concentrations of gaseous and particulate phase PAHs in the winter are 4300+/-2900 ng/m(3) and 750+/-1000 ng/m(3), respectively, significantly higher than those measured simultaneously at control sites and also considerably higher than the values measured during the summer. The exposure PAH profiles for police and the control subjects are similar with predominant naphthalene in gaseous phase and dominant fluoranthene, pyrene, anthracene and naphthalene in particulate phase. Large daily variations occur both in summer and winter, because of the changes in the weather conditions especially wind speed and relative humidity which tend to disperse and scavenge PAHs in air. In the winter, the average BaP(eq) value for traffic police is 82.1 ng/m(3), which is significantly higher than those for the control subjects and the national standard of 10 ng/m(3) for ambient air. Particulate phase PAHs contribute more than 90% of the total exposure risk in the winter. Annually, weighted-average probabilities of exceeding the national standard (10 ng/m(3)) are 69.3% and 20.6% for the police and the controls, respectively.     

Influence of residential wood combustion on local air quality

The importance of wood combustion to local air quality was estimated by measuring different air pollutants and conducting chemical mass balance modelling. PM10, PM2.5, PAHs and VOC concentrations in ambient air were measured in a typical Finnish residential area. Measurements were conducted in January-March 2006. For some compounds, wood combustion was clearly the main local source at this site. The effect of wood combustion was more clearly seen for organic compounds than for fine particle mass. For fine particles, background concentrations dominated. However, very high, short-lived concentration peaks were detected, when the wind direction and other weather conditions were favourable. For organic compounds, the effect of wood combustion was seen in diurnal and in two-week average concentrations. PAH-concentrations were often several times higher at the residential area than in the background. Benzene concentrations showed similar diurnal pattern as the use of wood and benzene/toluene ratios indicated that wood combustion is the most important source. A chemical mass balance model was used for studying the effect of wood combustion on the measured concentrations of VOCs. Model results showed that the main local sources for VOCs at Kurkim?ki are wood combustion and traffic. Wood combustion was clearly the most important source for many compounds (e.g., benzene).     

Comparison of particle-phase polycyclic aromatic hydrocarbons and their variability causes in the ambient air in Ho Chi Minh City, Vietnam and in Osaka, Japan, during 2005-2006

A comparative study of polycyclic aromatic hydrocarbons (PAHs) associated with particulate matter (TSP) in the ambient air in an urban area in Ho Chi Minh City, Vietnam and in Osaka, Japan was carried out from 2005 to 2006. The objective of this study was to investigate the environmental levels, emission sources, seasonal variations and health risk of eleven PAHs in the two cities, especially Ho Chi Minh City where air pollution is becoming a serious concern. The results showed that the concentrations of TSP and total PAHs were significantly higher in Ho Chi Minh City than levels in Osaka. The concentrations of 5- and 6-ring PAHs (BeP, BbF, BkF, BaP, BghiP and InP) were much higher in TSP samples in Ho Chi Minh City than in Osaka, accounting for 82% and 51% of total PAHs, respectively. These PAHs are known to be highly carcinogenic and mutagenic in humans. Vehicular emission is suggested as one of the main pollution sources of PAHs in both cities. Motorcycles and gasoline automobiles are suggested as the main emission sources of PAHs in Ho Chi Minh City, whereas diesel automobiles are the primary source in Osaka. Seasonal variations of PAHs were observed in this study; higher concentrations of PAHs were found in the rainy season (May-December) and lower concentrations corresponded to the dry season (February-April) in Ho Chi Minh City, while higher concentrations of PAHs were observed in the winter (November-January) in Osaka. The number of sunshine hours was an important meteorological factor affecting seasonal variations of PAHs in Ho Chi Minh City, while the temperature was a main factor causing the variations of PAHs in Osaka. The high BaP equivalent concentration of 5- and 6-ring PAHs even in the ambient air is an alarming signal for harmfulness to human health and environmental quality in Ho Chi Minh City.     

Characteristic of polycyclic aromatic hydrocarbon concentrations and source identification for fine and coarse particulates at Taichung Harbor near Taiwan Strait during 2004-2005

Fine (PM(2.5)) and coarse (PM(2.5-10)) particulate concentrations of ambient air polycyclic aromatic hydrocarbons (PAHs) were measured simultaneously from February 2004 to January 2005 at the Taichung Harbor (TH) sampling site near Taiwan of central Taiwan. Particle-bound polycyclic aromatic hydrocarbons (PAHs) were collected on quartz filters; the collected sample was Soxhlet extracted with a dichloromethane (DCM)/n-hexane mixture (50/50, v/v) for 24 h, and then the extracts were analyzed by gas chromatography-mass spectrometry (GC-MS). The results indicated that vehicle emissions, coal combustion, incomplete combustion and pyrolysis of fuel and oil burning were the main source of PAHs near Taiwan Strait of central Taiwan. Diagnostic ratios and principal component analysis (PCA) were also used to characterize and identify PAHs emission sources in this study.     

Sampling and analysis of gas-phase methylmercury in ambient air

A procedure for sampling gaseous methylmercury (MeHg) in ambient air using a refluxing mist chamber (MC) has been developed. The MC consists of a glass bulb with an air inlet tube at the bottom. Via a capillary mounted adjacent to the inlet tube, the solution inside the MC is pulled from the bottom of the bulb to form a mist inside the chamber. Two different aqueous sampling solutions were tested and evaluated, a dilute HCl (0.003 M) solution and a solution containing the chelating agent ammonium salt of pyrrolidine-1-dithiocarboxylic acid. The airflow rate through the sampler was 10-15 l min(-1). The sampling time was 6 h when using dilute HCl as an extraction solution, and 3 h when using the solution containing the chelating solution. Determination of atmospheric MeHg collected in the aerated water sample was accomplished using GC/CVAFS after aqueous phase ethylation, and pre-collection onto carbotrap column. To test the reproducibility and accuracy of the method, parallel sampling, and standard additions tests were carried out. Other quality control tests, i.e. procedure blanks and duplicated analysis have also been performed. The detection limit, based on three times the standard deviation of total blank (including sampling, distillation, and analysis) is 2 pg, which corresponds to a procedural detection limit of approximately 1 pgm(-3) in ambient air when sampling for 3 h. Measurements performed on the roof of the IVL building yielded concentrations from 3 to 22 pgm(-3) corresponding to 0.3-1% of the total gaseous mercury in ambient air.     

Distributions of polycyclic aromatic hydrocarbons in surface waters, sediments and soils of Hangzhou City, China

Ten polycyclic aromatic hydrocarbons (PAHs) were simultaneously measured in 17 surface water samples and 11 sediments of four water bodies, and 3 soils near the water-body bank in Hangzhou, China in December 2002. It was observed that the sum of PAHs concentrations ranged from 0.989 to 9.663 microg/L in surface waters, from 132.7 to 7343 ng/g dry weight in sediments, and from 59.71 to 615.8 ng/g dry weight in soils. The composition pattern of PAHs by ring size in water, sediment and soil were surveyed. Three-ring PAHs were dominated in surface waters and soils, meanwhile sediments were mostly dominated by four-ring PAHs. Furthermore, PAHs apparent distribution coefficients (K(d)) and solid f(oc)-normalized K(d) (e.g. K(oc)= K(d) / f(oc)) were calculated. The relationship between logK(oc) and logK(ow) of PAHs for field data on sediments and predicted values were compared. The sources of PAHs in different water bodies were evaluated by comparison of K (oc) values in sediments of the river downstream with that in soils. Hangzhou section of the Great Canal was heavily polluted by PAHs released from industrial wastewater in the past and now PAHs in sediment may serve as sources of PAHs in surface water. PAHs in Qiantang River were contributed from soil runoff. Municipal road runoff was mostly contributed to West Lake PAHs.     

Dependence of urban air pollutants on meteorology

Dependence of air pollutants on meteorology is presented with the aim of understanding the governing processes pollutants phase interaction. Intensive measurements of particulate matter (PM10) and gaseous materials (e.g., CO, NO2, SO2, and O3) are carried out regularly in 2002 at 14 measurement sites distributed over the whole territory of Great Cairo by the Egyptian Environmental Affairs Agency to assess the characteristics of air pollutants. The discussions in this work are based upon measurements performed at Abbassiya site as a case study. The nature of the contributing sources has been investigated and some attempts have been made to indicate the role played by neighboring regions in determining the air quality at the site mentioned. The results hint that, wind direction was found to have an influence not only on pollutant concentrations but also on the correlation between pollutants. As expected, the pollutants associated with traffic were at highest ambient concentration levels when wind speed was low. At higher wind speeds, dust and sand from the surrounding desert was entrained by the wind, thus contributing to ambient particulate matter levels. We also found that, the highest average concentration for NO2 and O3 occurred at humidity相似文献   

Atmospheric concentrations and air-soil gas exchange of polycyclic aromatic hydrocarbons (PAHs) in remote, rural village and urban areas of Beijing-Tianjin region, North China

Forty passive air samplers were deployed to study the occurrence of gas and particulate phase PAHs in remote, rural village and urban areas of Beijing-Tianjin region, North China for four seasons (spring, summer, fall and winter) from 2007 to 2008. The influence of emissions on the spatial distribution pattern of air PAH concentrations was addressed. In addition, the air-soil gas exchange of PAHs was studied using fugacity calculations. The median gaseous and particulate phase PAH concentrations were 222 ng/m³ and 114 ng/m³, respectively, with a median total PAH concentration of 349 ng/m³. Higher PAH concentrations were measured in winter than in other seasons. Air PAH concentrations measured at the rural villages and urban sites in the northern mountain region were significantly lower than those measured at sites in the southern plain during all seasons. However, there was no significant difference in PAH concentrations between the rural villages and urban sites in the northern and southern areas. This urban-rural PAH distribution pattern was related to the location of PAH emission sources and the population distribution. The location of PAH emission sources explained 56%-77% of the spatial variation in ambient air PAH concentrations. The annual median air-soil gas exchange flux of PAHs was 42.2 ng/m²/day from soil to air. Among the 15 PAHs measured, acenaphthylene (ACY) and acenaphthene (ACE) contributed to more than half of the total exchange flux. Furthermore, the air-soil gas exchange fluxes of PAHs at the urban sites were higher than those at the remote and rural sites. In summer, more gaseous PAHs volatilized from soil to air because of higher temperatures and increased rainfall. However, in winter, more gaseous PAHs deposited from air to soil due to higher PAH emissions and lower temperatures. The soil TOC concentration had no significant influence on the air-soil gas exchange of PAHs.     

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 (BaP_eq) of the benzo[a]pyrene values for PAHs were 0.14, 0.32, 1.38 and 3.59 ng m^− 3 in spring, summer, autumn and winter, respectively. Furthermore, the results of average BaP_eq in all four seasons indicated that the health risks of particulate PAHs were higher than those of the gaseous PAHs at different sampling sites.     

Results of a residential indoor PM2.5 sampling program before and after a woodstove changeout

During 2005-2007, a woodstove changeout program was conducted in a Rocky Mountain valley community in an effort to reduce ambient levels of PM(2.5). In addition to changes in ambient PM(2.5), an opportunity was provided to evaluate the changes in indoor air quality when old stoves were replaced with US Environmental Protection Agency (EPA)-certified woodstoves. PM(2.5) samples were measured in 16 homes prior to and following the changeout. For each sampling event, PM(2.5) mass was continuously measured throughout the 24-h sampling periods, and organic/elemental carbon (OC/EC) and associated chemical markers of woodsmoke were measured from quartz filters. Results showed that average PM(2.5) concentrations and maximum PM(2.5) concentrations were reduced by 71% and 76%, respectively (as measured by TSI DustTraks). Levoglucosan was reduced by 45% following the introduction of the new woodstove. However, the concentrations of resin acids, natural chemicals found in the bark of wood, were increased following the introduction of the new woodstove. There were no discernible trends in methoxphenol levels, likely due to the semi-volatile nature of the species that were measured. Although there is some uncertainty in this study regarding the amount of ambient PM infiltration to the indoor environment, these findings demonstrated a large impact on indoor air quality following this intervention. PRACTICAL IMPLICATIONS: Emissions from residential woodstoves are an important air quality issue (both indoors and ambient) in many regions throughout the US and the world. More specifically, woodstoves have been identified as a major source of PM(2.5) in valley locations throughout the Northern Rocky Mountains, where biomass combustion is the predominant source of home heating. In this study, we present results that demonstrate the dramatic reduction in PM(2.5) concentrations (as measured by TSI, Inc. DustTrak PM(2.5) air samplers) inside homes following the replacement of old, polluting woodstove with new EPA-certified woodstoves.     

Gas-particle partitioning and seasonal variation of polycyclic aromatic hydrocarbons in the atmosphere of Zonguldak, Turkey

Atmospheric concentrations and gas-particle partition coefficients were determined for polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of Zonguldak, Turkey between May 2007 and April 2008. Total concentrations of PAHs ranged from 0.52 ng m^− 3 to 636 ng m^− 3 in the particle phase and from 5.60 ng m^− 3 to 725 ng m^− 3 in the gas phase. The annual mean concentrations of PAHs in the particle and gas phase were found to be 114 ng m^− 3 and 184 ng m^− 3, respectively. Significant seasonal variations of particle and gas phase PAH concentrations were observed with higher levels during cold period. The distribution of PAHs between the particle and gas phase was investigated and it was found that three ring PAHs were associated primarily with the gas phase, four ring PAHs were distributed almost equally between the two phases and five and six ring PAHs were mainly associated with the particle phase. Gas-particle partition coefficients (K_p) of PAHs have been calculated and correlated with their subcooled liquid vapor pressures (P_Lº). The slopes (m_r) varied from − 0.63 to − 0.23 were far from the theoretical value (−1) due to the short distance between the sampling point and the emission sources. The relationships between temperature and gas phase partial pressures of PAHs were examined using the Clausius-Clapeyron equation and the obtained positive slopes indicated that PAH concentrations increased with decreasing air temperature as a result of high dominance of local emissions.     

Investigation of Lake Sapanca water pollution,Adapazari, Turkey

Lake Sapanca has been the only source of drinking and recreational water for the city of Adapazari, Turkey. This paper reports a study of the variation of nutrient loading and trophic state of the lake, and also water quality parameters of Lake Sapanca compared to those of the neighbouring Lake Iznik. Through one year, samples were taken every three months from 15 different points on the streams feeding and draining off the lake. Nitrate, NO₂‐N, NH₃‐N, TKN, PO₄‐P concentrations on the 12 streams fe and three draining off points were determined. Then, loading, discharge, and accumulation amounts of nitrogen and phosphorus causing eutrophication were calculated and the trophic state of the lake was determined. A simple model was used to analyse the response of Lake Sapanca when the phosphorus loading rate was changed. Through this model, the variation of different parameters (t, M, K, Q, V and A) with respect to phosphorus concentration (C) was studied to identify effects and results. The consequences of an eutrophic state and measures to protect the lake are also discussed.     

Mass balance for polycyclic aromatic hydrocarbons in the urban watershed of Le Havre (France): transport and fate of PAHs from the atmosphere to the outlet

Polycyclic aromatic hydrocarbon (PAH) concentrations have been monitored simultaneously in ambient air, bulk atmospheric deposition and runoff waters during one year in a small urban watershed of the Seine river basin (France). PAH fluxes from the atmosphere to the outlet of the urban watershed have been calculated to establish a mass balance for PAHs. PAH flux in runoff waters was 5.2 kg km(-2) yr(-1) while PAH atmospheric deposition was 0.21 kg km(-2) yr(-1). The comparison between atmospheric input and output by runoff has shown the importance of street deposits that appeared to be the most important source of PAHs for surface waters in urban areas. PAH profiles in the various compartments showed the fate of PAHs in the air-water system: proportion of carcinogenic PAHs was more important in runoff waters (35%) than in bulk atmospheric deposition (22%) and air (6%).