PAH levels in a furniture-manufacturing city atmosphere.

In this study, in order to determine atmospheric PAH concentrations in Inegol/Turkey, ambient air samples were collected from two different sites representing industrial and uncontrolled furniture manufacturers regions. Sampling campaign took place between December 2017 and November 2018. Air samples were collected using high volume air samplers (HVAS) and PAH concentrations were determined in both gas and particulate phases. The mean of the atmospheric PAH concentrations obtained in the gas phase in the furniture workshops (FW) and industrial district (ID) regions were 697.82 ±â€¯637 ng/m3 and 772.92 ±â€¯864.23 ng/m3, respectively. The concentrations in the particulate phase in the regions were 413.52 ±â€¯430.23 ng/m3 and 342.40 ±â€¯527.48 ng/m3, respectively. The average total (gas + particlulate phases) concentration of ∑16PAH determined in the site of FW was 1111.34 ±â€¯1045.24 ng/m3 while that was 772.92 ±â€¯864.23 ng/m3 in ID. These values are over the ambient levels reported for urban sites wherein big industries exist around the world. Additionally, the average of particle phase percentage was 30% because of nearby combustion sources. The determination of possible sources of PAHs in the regions was performed using principal component analysis (PCA). PCA results showed that the main sources of pollutants of the regions are intertwined (combustion, traffic, industries). However, the most effective source is thought to be uncontrolled combustion of furniture wastes as fuel for residential heating. Health risks for the citizens were calculated for both regions and were found not to be at high-class risk.

Levels of persistent organic pollutants in pine tree components and ambient air.

Pine needles are employed as alternative biomonitoring agents in atmospheric studies. In this study, pine (Pinus Pinea) components (needles and branches) and air samples were collected simultaneously to monitor polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) from Gemlik, Turkey between January and December 2016. The relationship between ambient air and pine needles were examined to enlighten the usability of pine components as passive samplers for persistent organic pollutants (POPs) in the Marmara region. Average ∑14PAH concentrations for the ambient air, pine needles, and pine branches were 23.1 ±â€¯18.3 ng/m3, 626 ±â€¯306 ng/g DW and 548 ±â€¯261 ng/g DW respectively. PCB concentrations were 118 ±â€¯74 pg/m3, 7.5 ±â€¯2.1 ng/g DW and 6.8 ±â€¯2.9 ng/g DW and ∑10 OCP concentrations were 122 ±â€¯89 ng/m3,1.3 ±â€¯1.5 ng/g DW and 10.0 ±â€¯3.8 ng/g DW in the same order. Levels of PAHs and PCBs were higher in needles than branches. PAH, PCB and OCP concentrations in pine components tended to decrease with increasing temperatures in spring. PAH compounds with medium and light molecular weighted ones were found to be dominant. On the other hand, the predominant PCB components were the medium-weighted congeners while γ-HCH, Heptachlor endo. Epox. Iso A, endrin aldehyde, and methoxychlor were the dominant OCP species.

Atmospheric deposition of organochlorine pesticides by precipitation in a coastal area.

Wet deposition fluxes of organochlorine pesticides (OCPs) were determined for rain samples collected in a coastal area of Turkey. Seventeen precipitation samples were collected over a 1-year period from 2008 to 2009. Rainwater was accumulated at the beginning of rain events using real time monitoring. Atmospheric concentrations were also measured in parallel with deposition samples. Both atmospheric concentrations and deposition fluxes were determined as particle and gas phases. The particle phase and dissolved phase deposition fluxes were 794.26 ± 756.70 ngm-2 day-1 and 800.77 ± 672.63 ngm-2 day-1, respectively. The washout ratios for OCP compounds were calculated separately for the particle and dissolved phases using the atmospheric concentrations and rain concentrations. The minimum washout ratio for the particle phase was 2339.47 for Endrin aldehyde, whereas the maximum washout ratio was 497593.34 for Methoxychlor. The maximum washout ratio for the dissolved phase was 247523.89 for Endosulfan beta, whereas the minimum washout ratio was 10169.69 for p,p'-DDT. The dry deposition velocities ranged from 0.01 to 1.67 cms-1. The partitioning of wet deposition between the particle and dissolved phases was 50 % in terms of total OCP deposition.

Migration of polycyclic aromatic hydrocarbons (PAHs) in urban treatment sludge to the air during PAH removal applications.

In the present study, the amounts of polycylic aromatic hydrocarbons (PAHs) penetrating into air during PAH removal applications from the urban treatment sludge were investigated. The effects of the temperature, photocatalyst type, and dose on the PAH removal efficiencies and PAH evaporation were explained. The sludge samples were taken from an urban wastewater treatment plant located in the city of Bursa, with 585,000 equivalent population. The ultraviolet C (UV-C) light of 254 nm wavelength was used within the UV applications performed on a specially designed setup. Internal air of the setup was vacuumed through polyurethane foam (PUF) columns in order to collect the evaporated PAHs from the sludge during the PAH removal applications. All experiments were performed with three repetitions. The PAH concentrations were measured by gas chromatography-mass spectrometry (GC-MS). It was observed that the amounts of PAHs penetrating into the air were increased with increase of temperature, and more than 80% of PAHs migrated to the air consisted of 3-ring compounds during the UV and UV-diethylamine (DEA) experiments at 38 and 53 degrees C. It was determined that 40% decrease was ensured in sigma12 (total of 12) PAH amounts with UV application and 13% of PAHs in sludge penetrated into the air. In the UV-TiO2 applications, a maximum 80% of sigma12 PAH removal was obtained by adding 0.5% TiO2 of dry weight of sludge. The quantity of PAH penetrating into air did not exceed 15%. UV-TiO2 applications ensured high levels of PAH removal in the sludge and also reduced the quantity of PAH penetrating into the air. Within the scope of the samples added with DEA, there was no increase in PAH removal efficiencies and the penetration of PAHs into air was not decreased. In light of these data, it was concluded that UV-TiO2 application is the most suitable PAH removal alternative that restricts the convection of PAH pollution.

Atmospheric organochlorine pesticide (OCP) levels in a metropolitan city in Turkey.

Air concentrations of organochlorine pesticides (OCPs) were measured at four different sites in Bursa, Turkey to determine current levels. For this purpose, about 35 samples were collected from June 2008 to June 2009 using a high volume air sampler (HVAS) equipped with particle and gas-phase units. Ten OCP compounds (alpha-, beta-, gamma-, delta-hexachlorocyclohexane, Heptachlor epoxide, Endrin, Endosulfan beta, Endrin aldehyde, p,p'-DDT and Methoxychlor) were reported within the scope of this study. The average concentrations of total (particle+gas) ∑OCPs were 550.9 ± 277.6 pg m⁻³ (coastal), 1030.7 ± 453.5 pg m⁻³ (urban/traffic), 519.7 ± 277.5 pg m⁻³ (semi-rural) and 722.8 ± 351.8 pg m⁻³ (urban/residential). The individual OCP concentrations were in line with reported concentrations. The maximum particle and gas-phase concentrations were determined for Endosulfan beta and beta-HCH for all sites, respectively. Available gas/particle partitioning models were applied in order to investigate the compatibility of the experimental data and the significant relationships were observed.

Ambient air levels and trends of polychlorinated biphenyls at four different sites.

In this study, samples were collected in order to determine atmospheric levels of polychlorinated biphenyls (PCBs) in four different sites by using a high-volume air sampler (HVAS). Eighty-three congeners of gas and particle- phase PCBs were investigated in air samples. The total (gas + particle) concentrations for Mudanya (coastal), Butal (traffic/urban), the Uludag University Campus (semirural), and Yavuz Selim (residential) were determined as 570, 394, 412, and 316 pg/m(3), respectively. These levels coincide with the values reported for the sites having similar characteristics. In terms of homolog groups, 3-chlorinated biphenyls (3-CBs) and 4-CBs constituted at least 47% of the total PCB concentration. PCBs in all sites were determined mostly in the gas phase, with a percentage from 85 to 95%. Obtained atmospheric PCB data were correlated with meteorological parameters and a significant relationship was obtained between coastal and semirural sites (p < 0.05). With the movements of air transportation and wind rose possible data sources of PCBs were enlightened. Partitioning of gas/particle was examined with available models; significant relationships were determined for coastal and semirural sites especially.

Comparison of polycyclic aromatic hydrocarbons levels in sludges from municipal and industrial wastewater treatment plants.

This study was carried out to investigate the concentrations and potential sources of the polycyclic aromatic hydrocarbons (PAHs) in sludge of 14 wastewater treatment plants (WWTPs). Sludge samples were collected from 2 municipal WWTPs, 11 industrial WWTPs, and 1 sanitary landfill leachate treatment plant within the city of Bursa, Turkey during the summer of 2008. Ultrasonication was applied for extraction and gas chromatography-mass spectrometry was used to analyze the PAH contents of the samples. Twelve of the 16 EPA-listed PAH compounds were determined. Total PAH concentrations (Sigma(12) PAHs) determined in all of the sludge samples ranged from 1,781 to 19,866 microg/kg dry matter (dm). The sum of 8 of the 11 EU PAHs varied between 1,481 and 17,314 microg/kg dm, and 3 of the samples exceeded the proposed EU limit for land application. One of the automotive industry sludges contained the highest level of PAHs, followed by one of the municipal sludges. The average sum of 5- and 6-ring PAH compounds in all of the sludge samples amounted to almost 65% of the total PAHs. The diagnostic ratios of specific PAHs were calculated to determine the dominant sources for the PAHs in the sludge samples.

Dynamics of atmospheric polychlorinated biphenyls (PCBs): concentrations, patterns, partitioning, and dry deposition level estimations in a residential site of Turkey.

Air samples were collected at a residential site (Gulbahce, Bursa, Turkey) between August 2004 and April 2005 using a modified high volume air sampler. The mean of gas and particle phase concentrations of polychlorinated biphenyls (PCBs) were 468 +/- 297 and 43 +/- 37 pg m(-3) (average +/- standard deviation, SD), respectively. The dominated PCB homologs were 3-CBs, 4-CBs, and 5-CBs. The measured PCB concentrations were higher than the values of pristine sites. In order to assess the gas/particle partitioning fate, log K(P)-log P(o)(L), log K(P)-log K (OA) and the Junge-Pankow model were applied to the data. Experimental K(P) was well correlated with log P(o)(L) and log K(OA) at p < 0.05. Then, dry deposition fluxes were estimated using atmospheric concentrations and dry deposition velocities obtained from literature. A correlation matrix was formed for PCB homologs including 27 congeners with concurrently measured 16 polycyclic aromatic hydrocarbons (PAHs) and meteorological parameters. Most of PAH compounds were significantly correlated with 5-CBs and 6-CBs.

Bulk deposition of polycyclic aromatic hydrocarbons (PAHs) in an industrial site of Turkey.

Ambient air and deposition samples were collected in the period of July 2004-May 2005 in an industrial district of Bursa, Turkey and analyzed for polycyclic aromatic hydrocarbon (PAH) compounds. The overall average of fourteen bulk deposition fluxes for PAHs was 3300+/-5100 ng m(-2) d(-1). PAH depositions showed a seasonal variation and they were higher in winter months. This was probably due to increases in residential heating activities and decreases in atmospheric mixing layer levels. Ambient air samples, measured with a high volume air sampler, were collected from the same site. The average total concentration including gas and particulate phase was about 300+/-420 ng m(-3) and it was in the range of previously reported values. Some of the ambient air and bulk deposition samples were collected simultaneously in dry periods. Both concurrently measured values were used to calculate the dry deposition velocities whose overall average value was 0.45+/-0.35 cm s(-1).

The determination of gas phase dry deposition fluxes and mass transfer coefficients (MTCs) of polychlorinated biphenyls (PCBs) using a modified water surface sampler (WSS).

Gas phase PCB dry deposition and concentration samples were collected simultaneously between July 2004 and May 2005 at a suburban site in Bursa, Turkey. A modified water surface sampler (WSS) was employed to collect gas phase fluxes while a high-volume air sampler (HVAS) was used for concentration samples. The WSS was able to collect both particle and gas phase PCB deposition samples. The collected PCBs on water surface were captured by a filter and an XAD-2 resin column during water cycle. The average of gas phase PCB deposition flux, determined by analyzing the XAD-2 resin column, was 79.3+/-40.5 ng m(-2) d(-1) and its percentage in total (gas+particle) PCB flux was about 60. The average of gas phase PCB concentration measured concurrently with flux samples was 224.4+/-160.2 pg m(-3) and its ratio to the total (gas+particle) PCB concentration was 85%. This difference was likely due to the different deposition characteristics of gases and particulates. Dominant PCB homolog groups were 3-4 chlorobiphenyls (CBs) for both ambient air and gas phase deposition samples. Mass transfer coefficients (MTC, K(g)) for air-side were determined using gas phase flux and ambient air concentration values. The average overall K(g) ranged between 0.21 and 0.96 cm s(-1) with an average of 0.60+/-0.19 cm s(-1).

Monitoring of criteria air pollutants in Bursa, Turkey.

The concentrations of criteria air pollutants such as CO, NOx (NO + NO2), SO2 and PM were measured in the period of May 2001 and April 2003 in the city of Bursa, Turkey. The average concentrations for this period were 1115 +/- 1600 microg/m3, 29 +/- 50 microg/m3, 51 +/- 24 microg/m3, 79 +/- 65 microg/m3, 40 +/- 35 microg/m3, 98 +/- 220 microg/m3, for CO, NO, NO2, NOx, SO2 and PM, respectively. Temporal changes in concentrations were analyzed using meteorological factors. Correlations among pollutant concentrations and meteorological parameters showed weak relations nearly in all data. Lower concentrations were observed in the summer months while higher concentrations were measured in the winter months. The increase in winter concentrations was probably due to residential heating. Pollutants were associated with each other in order to have information about their origin. NOx/SO2 ratio was also examined to bring out the source origin contributing on air pollution (i.e., traffic or stationary).