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: 91
    Citation - Scopus: 95
    Source Apportionment and Carcinogenic Risk Assessment of Passive Air Sampler-Derived Pahs and Pcbs in a Heavily Industrialized Region
    (Elsevier Ltd., 2018) Çetin, Banu; Yurdakul, Sema; Güngörmüş, Elif; Öztürk, Fatma; Sofuoğlu, Sait Cemil
    Cancer has become the primary reason of deaths in Dilovasi probably due to its location with unique topography under the influence of heavy industrialization and traffic. In this study, possible sources and carcinogenic health risks of PAHs and PCBs were investigated in Dilovasi region by Positive Matrix Factorization (PMF) and the USEPA approach, respectively. PAHs and PCBs were measured monthly for a whole year at 23 sampling sites using PUF disk passive samplers. Average ambient air concentrations were found as 285 ± 431 ng/m 3 and 4152 ± 6072 pg/m 3 , for Σ 15 PAH and Σ 41 PCB, respectively. PAH concentrations increased with decreasing temperature especially at urban sites, indicating the impact of residential heating in addition to industrial activities and traffic. On the other hand, PCB concentrations mostly increased with temperature probably due to enhanced volatilization from their sources. Possible sources of PAHs were found as emissions of diesel and gasoline vehicles, biomass and coal combustion, iron and steel industry, and unburned petroleum/petroleum products, whereas iron-steel production, coal and biomass burning, technical PCB mixtures, and industrial emissions were identified for PCBs. The mean carcinogenic risk associated with inhalation exposure to PAHs and PCBs were estimated to be >10 −6 and >10 −5 , respectively, at all sampling points, while the 95th percentile was >10 −5 at 15 of 23 and >10 −4 at 8 of 23 sampling locations, respectively. Probabilistic assessment showed, especially for PCBs, that a majority of Dilovasi population face significant health risks. The higher risks due to PCBs further indicated that PCBs and possibly other pollutants originating from the same sources such as PBDEs and PCNs may be an important issue for the region.
  • Article
    Citation - WoS: 33
    Citation - Scopus: 35
    Henry'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, Aysun
    The 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: 50
    Citation - Scopus: 55
    Determination of Henry's Law Constants of Organochlorine Pesticides in Deionized and Saline Water as a Function of Temperature
    (Elsevier Ltd., 2006) Çetin, Banu; Özer, Serdar; Sofuoğlu, Aysun; Odabaşı, Mustafa
    The Henry's law constant (H) is an important parameter that is required to estimate the air-water exchange of semi-volatile organic compounds. Henry's law constants for 17 banned/restricted/currently used organochlorine pesticides (OCPs) were experimentally determined using a gas-stripping technique in deionized and saline water (3%) over a temperature range of 5-35 °C. H values (at 25 °C) ranged between 0.066±0.037 Pa m3 mol-1 (endosulfan II) and 62.0±24.2 Pa m3 mol-1 (heptachlor) in deionized water while the range in saline water was 0.28±0.03 Pa m3 mol-1 (γ-HCH) and 135.2±31.3 Pa m3 mol-1 (heptachlor). The increase in dimensionless Henry's law constants (H′) for OCPs over the studied temperature range was between 3 (γ-HCH)-19 times (chlorpyrifos) and 3 (endosulfan II)-80 times (trans-nonachlor) in deionized and saline water, respectively. The calculated enthalpies of phase change (ΔHH) were within the ranges previously reported for OCPs and other organic compounds (23.8-100.2 kJ mol-1). The salting-out constant, ks, ranged between 0.04 (γ-HCH) and 1.80 L mol-1 (endosulfan II) indicating the importance of assessing the H values of OCPs in saline water to accurately determine their partitioning and fate in seawater.
  • Article
    Determination of Henry's Law Constants of Organochlorine Pesticides in Deionized and Saline Water as a Function of Temperature
    (Elsevier Ltd., 2006) Çetin, Banu; Özer, Serdar; Sofuoğlu, Aysun; Odabaşı, Mustafa
    The publisher regrets that the second paragraph on p. 4545 was printed incorrectly. It now appears correctly, below. The presence of salts in aqueous solution affects the solubility of organic molecules, through the salting-out effect (Demou and Donaldson, 2002). The salting-out is defined as the decrease in aqueous solubility and increase in the activity coefficient observed for neutral non-polar compounds by dissolved inorganic salts. Ions in solution tightly bind several water molecules into hydration shells. This process (electrostriction), results in a reduction of the volume of the aqueous solution. A smaller aqueous volume results in less available water for cavity formation, and therefore less organic molecules are accommodated; their solubility decreases as a consequence (Schwarzenbach et al., 2002; Demou and Donaldson, 2002). The empirical relation for the effect of ionic strength on Henry’s law constant is described by Setschenow equation (Demou and Donaldson, 2002):