Sürdürülebilir Yeşil Kampüs Koleksiyonu / Sustainable Green Campus Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7755
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Article Citation - WoS: 108Citation - Scopus: 113Spatial and Seasonal Variations, Sources, Air-Soil Exchange, and Carcinogenic Risk Assessment for Pahs and Pcbs in Air and Soil of Kutahya, Turkey, the Province of Thermal Power Plants(Elsevier Ltd., 2017) Dumanoğlu, Yetkin; Gaga, Eftade O.; Güngörmüş, Elif; Sofuoğlu, Sait Cemil; Odabaşı, MustafaAtmospheric and concurrent soil samples were collected during winter and summer of 2014 at 41 sites in Kutahya, Turkey to investigate spatial and seasonal variations, sources, air-soil exchange, and associated carcinogenic risks of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). The highest atmospheric and soil concentrations were observed near power plants and residential areas, and the wintertime concentrations were generally higher than ones measured in summer. Spatial distribution of measured ambient concentrations and results of the factor analysis showed that the major contributing PAH sources in Kutahya region were the coal combustion for power generation and residential heating (48.9%), and diesel and gasoline exhaust emissions (47.3%) while the major PCB sources were the coal (thermal power plants and residential heating) and wood combustion (residential heating) (45.4%), and evaporative emissions from previously used technical PCB mixtures (34.7%). Results of fugacity fraction calculations indicated that the soil and atmosphere were not in equilibrium for most of the PAHs (88.0% in winter, 87.4% in summer) and PCBs (76.8% in winter, 83.8% in summer). For PAHs, deposition to the soil was the dominant mechanism in winter while in summer volatilization was equally important. For PCBs, volatilization dominated in summer while deposition was higher in winter. Cancer risks associated with inhalation and accidental soil ingestion of soil were also estimated. Generally, the estimated carcinogenic risks were below the acceptable risk level of 10− 6. The percentage of the population exceeding the acceptable risk level ranged from < 1% to 16%, except, 32% of the inhalation risk levels due to PAH exposure in winter at urban/industrial sites were > 10− 6.Article Citation - WoS: 20Citation - Scopus: 26Pops in a Major Conurbation in Turkey: Ambient Air Concentrations, Seasonal Variation, Inhalation and Dermal Exposure, and Associated Carcinogenic Risks(Springer Verlag, 2016) Ugranlı, Tuğba; Güngörmüş, Elif; Kavcar, Pınar; Demircioğlu, Eylem; Odabaşı, Mustafa; Sofuoğlu, Sait Cemil; Lammel, Gerhard; Sofuoglu, AysunSemi-volatile organic compounds were monitored over a whole year, by collection of gas and particle phases every sixth day at a suburban site in Izmir, Turkey. Annual mean concentrations of 32 polychlorinated biphenyls (∑32PCBs) and 14 polycyclic aromatic hydrocarbons (∑14PAHs) were 348 pg/m3 and 36 ng/m3, respectively, while it was 273 pg/m3 for endosulfan, the dominant compound among 23 organochlorine pesticides (OCPs). Monte Carlo simulation was applied to the USEPA exposure-risk models for the estimation of the population exposure and carcinogenic risk probability distributions for heating and non-heating periods. The estimated population risks associated with dermal contact and inhalation routes to ∑32PCBs, ∑14PAHs, and some of the targeted OCPs (α-hexachlorocyclohexane (α-HCH), β-hexachlorocyclohexane (β-HCH), heptachlor, heptachlor epoxide, α-chlordane (α-CHL), γ-chlordane (γ-CHL), and p,p′-dichlorodiphenyltrichloroethane (p,p′-DDT)) were in the ranges of 1.86 × 10−16–7.29 × 10−9 and 1.38 × 10−10–4.07 × 10−6, respectively. The inhalation 95th percentile risks for ∑32PCBs, ∑14PAHs, and OCPs were about 6, 3, and 4–7 orders of magnitude higher than those of dermal route, respectively. The 95th percentile inhalation risk for ∑32PCBs and OCPs in the non-heating period were 1.8- and 1.2–4.6 folds higher than in the heating period, respectively. In contrast, the 95th percentile risk levels for ∑14PAHs in the heating period were 4.3 times greater than that of non-heating period for inhalation, respectively. While risk levels associated with exposure to PCBs and OCPs did not exceed the acceptable level of 1 × 10−6, it was exceeded for 47 % of the population associated with inhalation of PAHs with a maximum value of about 4 × 10−6.Article Citation - WoS: 58Citation - Scopus: 65Particle-Phase Dry Deposition and Air–soil Gas Exchange of Polycyclic Aromatic Hydrocarbons (pahs) in Izmir, Turkey(Elsevier Ltd., 2011) Demircioğlu, Eylem; Sofuoğlu, Aysun; Odabaşı, MustafaAmbient air and dry deposition samples were collected at suburban and urban sites in Izmir, Turkey. Atmospheric total (particle + gas) 14PAHs concentrations were 36±39 and 144±163 ngm−3 for suburban and urban sites, respectively. Phenanthrene was the most abundant compound at all sites, and all samples were dominated by low molecular weight PAHs. Average particulate 14PAH dry deposition fluxes were 8160±5024 and 4286±2782 ngm−2 day−1 and overall average particulate dry deposition velocities were 1.5±2.4 and 1.0±2.3cms−1 for suburban and urban sites, respectively. Soil samples were collected at suburban site. Average soil concentration for 14PAH was 55.9±14.4 ng g−1 dry weight. Calculated gas-phase air–soil exchange fluxes indicated that fluorene, phenanthrene, anthracene, and carbazole were deposited to soil in winter while they were volatilized in summer. Other compounds (fluoranthene-benzo[g,h,i]perylene) were deposited to soil in both periods. Annual average fluxes of PAHs representing soil to air (i.e., gas volatilization) and air to soil transfer (i.e., gas absorption, dry deposition, and wet deposition) processes were also compared. All processes were comparable for 14PAHs however their input was dominated by gas absorption. Gas absorption dominated for lower molecular weight PAHs, however dry deposition dominated for higher molecular weight PAHs. The results have suggested that for fluorene, soil and air may be approaching a steady state condition. For the remaining compounds, there was a net accumulation into the soil.Article Citation - WoS: 33Citation - Scopus: 35Henry's Law Constant, Octanol-Air Partition Coefficient and Supercooled Liquid Vapor Pressure of Carbazole as a Function of Temperature: Application To Gas/Particle Partitioning in the Atmosphere(Elsevier Ltd., 2006) Odabaşı, Mustafa; Çetin, Banu; Sofuoğlu, AysunThe Henry's law constant for carbazole was experimentally determined between 5 and 35°C using a gas-stripping technique. The following equation was obtained for dimensionless Henry's law constant (H′) versus temperature (T, K):lnH′=-3982(T,K)-1+1.01 Temperature-dependent octanol-air partition coefficients (KOA) and supercooled liquid vapor pressures (PL, Pa) of carbazole were also determined using the GC retention time method. The temperature dependence of KOA and PL were explained by the following:logKOA=4076/(T,K)-5. 65logPL(Pa)=-3948(T,K)-1+11.84 The gas and particle-phase carbazole concentrations measured previously in Chicago, IL in 1995 was used for gas/particle partitioning modeling. Octanol based absorptive partitioning model consistently underpredicted the gas/particle partition coefficients (K p) for all sampling periods. However, overall there was a good agreement between the measured Kp and soot-based model predictions.Article Citation - WoS: 42Citation - Scopus: 50Occurrence, Oral Exposure and Risk Assessment of Volatile Organic Compounds in Drinking Water for Izmir(Elsevier Ltd., 2006) Kavcar, Pınar; Odabaşı, Mustafa; Kitiş, Mehmet; İnal, Fikret; Sofuoğlu, Sait CemilConcentrations of volatile organic compounds (VOCs) were measured in the drinking water in Province of İzmir, Turkey, and associated health risks due to ingestion of these compounds were investigated using population weighted random samples. A total of 100 houses were visited in different districts of İzmir and drinking water samples were collected from consumers' drinking water source. Questionnaires were administered to one participant in each house to determine demographics and drinking water consumption rates. Oral exposure and risks were estimated for each participant and İzmir population by deterministic and probabilistic approaches, respectively. The four trihalomethane (THM) species (i.e., chloroform, bromodichloromethane, dibromochloromethane, and bromoform), benzene, toluene, p-xylene, and naphthalene were the most frequently detected VOCs with concentrations ranging from below detection limit to 35 μg/l. The risk estimates were found to be less than the values reported in the literature with few exceptions. Noncarcinogenic risks attributable to ingestion of VOCs for İzmir population were negligible, whereas the mean carcinogenic risk estimates for bromodichloromethane and dibromochloromethane were above the de minimis level of one in a million (10-6). For all VOCs, the concentrations measured in metropolitan area were greater than those in other districts. All THM species were detected in higher concentrations in tap water, whereas nontap water contained more benzene, toluene, p-xylene, and naphthalene. Therefore, the concentrations of the latter four compounds and associated risks increased with increasing income and education level since bottled water was used in larger proportions within these subgroups. The results of this study showed that oral exposure to drinking water contaminants and associated risks may be higher than the acceptable levels even if the concentrations fall below the standards.