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: 15Citation - Scopus: 19Brominated Flame Retardants in a Computer Technical Service: Indoor Air Gas Phase, Submicron (pm1) and Coarse (pm10) Particles, Associated Inhalation Exposure, and Settled Dust(Elsevier Ltd., 2019) Genişoğlu, Mesut; Sofuoğlu, Aysun; Kurt Karakuş, Perihan Binnur; Birgül, Aşkın; Sofuoğlu, Sait CemilBrominated flame retardants (BFRs) are found in multi-media indoors, therefore, may pose serious risks to human health. This study investigated the occurrence of BFRs in particulate matter (PM1 and PM10) and gas phase by active and passive sampling, and settled dust to estimate potential exposure in a computer technical service. Polybrominated diphenyl ethers (PBDEs) and their alternatives (novel BFRs, NBFRs) were studied. PM and gas phase were collected on glass fiber filters and polyurethane foam plugs, respectively, and analyzed with a GC/MS after extraction, clean-up, and concentration. Inhalation exposure of the staff was estimated based on the measured concentrations using Monte Carlo simulation. BDE-209 was the dominating PBDE congener in all media while bis(2-ethylhexyl)-3,4,5,6-tetrabromophthalate and 1,2-bis(2,4,6-tribromophenoxy)ethane were those of NBFRs. Submicron particulate matter (PM1) BFR levels constituted about one half of the PM10-associated concentrations, while average PM10 mass concentration (69.9 μg m−3) was nine times that of PM1 (7.73 μg m−3). Calculated log10 dust-gas and PM-gas partitioning coefficients ranged from −5.03 to −2.10, −2.21 to −0.55, and −2.26 to −1.04 for settled dust, PM10, and PM1, respectively. The indoor/outdoor concentration ratios were >1 for all compounds indicating the strength of indoor sources in the service. The estimated potential inhalation exposures, for future chronic-toxic and carcinogenic risk assessments, indicated that the levels of gas-phase and PM1-associated exposures were similar at approximately one half of PM10-associated levels. Results of this study indicate that the occurrence of BFRs in all studied media should be taken into consideration for occupational health mitigation efforts.Article Citation - WoS: 91Citation - Scopus: 95Source 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 CemilCancer 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: 45Citation - Scopus: 45The First Countrywide Monitoring of Selected Pops: Polychlorinated Biphenyls (pcbs), Polybrominated Diphenyl Ethers (pbdes) and Selected Organochlorine Pesticides (ocps) in the Atmosphere of Turkey(Elsevier Ltd., 2018) Kurt Karakuş, Perihan Binnur; Ugranlı Çiçek, Tuğba; Sofuoğlu, Sait Cemil; Çelik, Halil; Güngörmüş, Elif; Gedik, Kadir; Sofuoğlu, Aysun; Ökten, Hatice Eser; Birgül, Aşkın; Alegria, Henry; Jones, Kevin C.Atmospheric levels of 43 PCBs, 22 OCPs, and 14 PBDEs were determined in 16 cities at urban and rural sites by passive sampling to generate the first large-scale nationwide dataset of POP residues in Turkey's atmosphere. Sampling campaign was performed from May 2014 to April 2015 with three-month sampling periods at locations on east-west and north-south transects through the country to investigate seasonal and spatial variations, including long range atmospheric transport (LRAT). Factor analysis was conducted to infer on the potential sources. Overall average Σ43PCBs concentration was 108 ± 132 pg/m3. PCB-118 (26.3 ± 44.6 pg/m3) was the top congener, and penta-CBs had the highest contribution with 54.3%. ΣDDTs had the highest annual mean concentration with 134 ± 296 pg/m3 among the OCP groups among which the highest concentration compound was p'p-DDE (97.6 ± 236 pg/m3). Overall average concentration of Σ14PBDEs was 191 ± 329 pg/m3 with the highest contribution from BDE-190 (42%). Comparison of OCPs and PCBs concentrations detected at temperatures which were above and below annual average temperature indicated higher concentrations in the warmer periods, hence significance of secondary emissions for several OCPs and Σ43PCBs, as well as inference as LRAT from secondary emissions. The first nationwide POPs database constructed in this study, point to current use, local secondary emissions, and LRAT for different individual compounds, and indicate the need for regular monitoring. The first country-wide passive sampling of selected POPs showed no unequivocal trends reflecting transitional location of Turkey.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: 89Citation - Scopus: 105Spatial and Temporal Variations in Atmospheric Vocs, No2, So2, and O3 Concentrations at a Heavily Industrialized Region in Western Turkey, and Assessment of the Carcinogenic Risk Levels of Benzene(Elsevier Ltd., 2015) Yılmaz Civan, Mihriban; Elbir, Tolga; Seyfioğlu, Remzi; Kuntasal, Öznur Oğuz; Bayram, Abdurrahman; Doğan, Güray; Yurdakul, Sema; Andiç, Özgün; Müezzinoğlu, Aysen; Sofuoğlu, Sait Cemil; Pekey, Hakan; Pekey, Beyhan; Bozlaker, Ayşe; Odabaşı, Mustafa; Tuncel, GürdalAmbient concentrations of volatile organic compounds (VOCs), nitrogen dioxide (NO2), sulphur dioxide (SO2) and ground-level ozone (O3) were measured at 55 locations around a densely populated industrial zone, hosting a petrochemical complex (Petkim), a petroleum refinery (Tupras), ship-dismantling facilities, several iron and steel plants, and a gas-fired power plant. Five passive sampling campaigns were performed covering summer and winter seasons of 2005 and 2007. Elevated concentrations of VOCs, NO2 and SO2 around the refinery, petrochemical complex and roads indicated that industrial activities and vehicular emissions are the main sources of these pollutants in the region. Ozone concentrations were low at the industrial zone and settlement areas, but high in rural stations downwind from these sources due to NO distillation. The United States Environmental Protection Agency's positive matrix factorization receptor model (EPA PMF) was employed to apportion ambient concentrations of VOCs into six factors, which were associated with emissions sources. Traffic was found to be highest contributor to measured ∑VOCs concentrations, followed by the Petkim and Tupras.Median cancer risk due to benzene inhalation calculated using a Monte Carlo simulation was approximately 4 per-one-million population, which exceeded the U.S. EPA benchmark of 1 per one million. Petkim, Tupras and traffic emissions were the major sources of cancer risk due to benzene inhalation in the Aliaga airshed. Relative contributions of these two source groups changes significantly from one location to another, demonstrating the limitation of determining source contributions and calculating health risk using data from one or two permanent stations in an industrial area.Article Citation - WoS: 37Citation - Scopus: 39Inhalation and Dermal Exposure To Atmospheric Polycyclic Aromatic Hydrocarbons and Associated Carcinogenic Risks in a Relatively Small City(Elsevier Ltd., 2014) Güngörmüş, Elif; Tuncel, Semra; Tecer, Lokman Hakan; Sofuoğlu, Sait CemilThe aim of this study was to conduct a carcinogenic risk assessment for exposure to polycyclic aromatic hydrocarbons (PAHs) via routes of inhalation and dermal contact. Concentrations of 19 PAH species were determined during a heating period at a site in the city of Balikesir, Turkey. Two questionnaires were administered to a sample of inhabitants to determine time-activity budgets and demographic information. The assessment was conducted for each participant and Balikesir population by deterministic and probabilistic approaches, respectively. Monte Carlo simulation was implemented to determine the population exposure-risk probability distributions. The estimates were based on benzo[a]pyrene equivalent (BaPeq) total PAH concentrations calculated using toxic equivalency factors. The mean and median BaPeq concentrations of gaseous and particulate phases were 3.25 and 1.34, and 38.5 and 34.0ng/m3, respectively. Carcinogenic risk for inhalation exposure route was estimated by using two different slope factor values (3.9 and 304.5(mg/kg-day)-1), recommended by two different organizations, resulting in two (order(s) of magnitude apart) population risk ranges: 1.32×10-7-2.23×10-4, and 1.61×10-5-7.95×10-3, respectively. The population risks associated with dermal exposure were lower compared to those of inhalation, ranging from 6.58×10-9 to 2.57×10-6. The proportion of the population with risks higher than the general acceptable level (1.0×10-6) was estimated as >99 percent, for inhalation, and as 28 percent for dermal exposure route.Article Citation - WoS: 45Citation - Scopus: 48Halogenated Volatile Organic Compounds in Chlorine-Bleach Household Products and Implications for Their Use(Elsevier Ltd., 2014) Odabaşı, Mustafa; Elbir, Tolga; Dumanoğlu, Yetkin; Sofuoğlu, Sait CemilIt was recently shown that substantial amounts of halogenated volatile organic compounds (VOCs) are formed in chlorine-bleach-containing household products as a result of reactions of sodium hypochlorite with organic product components. Use of these household products results in elevated indoor air halogenated VOC concentrations. Halogenated VOCs in several chlorine-bleach-containing household products (plain, n=9; fragranced, n=4; and surfactant-added, n=29) from Europe and North America were measured in the present study. Chloroform and carbon tetrachloride were the dominating compounds having average concentrations of 9.5±29.0 (average±SD) and 23.2±44.3 (average±SD) mgL-1, respectively. Halogenated VOC concentrations were the lowest in plain bleach, slightly higher in fragranced products and the highest in the surfactant-added products. Investigation of the relationship between the halogenated VOCs and several product ingredients indicated that chlorinated VOC formation is closely related to product composition. Indoor air concentrations from the household use of bleach products (i.e., bathroom, kitchen, and hallway cleaning) were estimated for the two dominating VOCs (chloroform and carbon tetrachloride). Estimated indoor concentrations ranged between 0.5 and 1030 (34±123, average±SD) μgm-3 and 0.3-1124 (82±194, average±SD) μgm-3 for chloroform and carbon tetrachloride, respectively, indicating substantial increases compared to background. Results indicated that indoor air concentrations from surfactant-added products were significantly higher (p<0.01) than other categories. The highest concentrations were from the use of surfactant-added bleach products for bathroom cleaning (92±228 and 224±334μgm-3, average±SD for chloroform and carbon tetrachloride, respectively). Associated carcinogenic risks from the use of these products were also estimated. The risk levels may reach to considerably high levels for a significant portion of the population especially for those steadily using the surfactant-added bleach products. Based on the results of the present study, it could be recommended that if possible the use of chlorine bleach containing household products should be avoided. If they are to be used, plain products should be preferred since the chlorinated VOC content increase with the number and amount of additives.Article Citation - WoS: 15Citation - Scopus: 15Atmospheric Concentrations and Potential Sources of Pcbs, Pbdes, and Pesticides To Acadia National Park(Elsevier Ltd., 2013) Sofuoğlu, Sait Cemil; Sofuoğlu, Aysun; Holsen, Thomas M.; Alexander, Colleen M.; Pagano, James J.This study assessed concentrations and investigated potential source regions for PCBs, PBDEs, and organochlorine pesticides in Acadia National Park, Maine, USA. Back-trajectories and potential source contribution function (PSCF) values were used to map potential source areas for total-PCBs, BDE-47, and 10 organochlorine pesticides. The constructed PSCF maps showed that ANP receives high pollutant concentrations in air masses that travel along four main pathways: (1) from the SW along the eastern Atlantic seaboard, (2) from the WSW over St. Louis, and Columbus regions, (3) from the west over Chicago, and Toronto regions, and (4) from WNW to NNW over the Great Lakes, and Quebec regions. Transport of all studied pollutants were equally distributed between the first three pathways, with only minor contributions from the last pathway. This study concludes that the high-pollutant concentrations arriving at ANP do not exclusively originate from the major urban centers along the eastern Atlantic seaboard.Article Citation - WoS: 23Citation - Scopus: 22Exposure To Particulate Matter in a Mosque(Elsevier Ltd., 2012) Ocak, Yılmaz; Kılıçvuran, Akın; Eren, Aykut Balkan; Sofuoğlu, Aysun; Sofuoğlu, Sait CemilIndoor air quality in mosques during prayers may be of concern for sensitive/susceptible sub-groups of the population. However, no indoor air pollutant levels of potentially toxic agents in mosques have been reported in the literature. This study measured PM concentrations in a mosque on Friday when the mid-day prayer always receives high attendance. Particle number and CO 2 concentrations were measured on nine sampling days in three different campaigns before, during, and after prayer under three different cleaning schedules: vacuuming a week before, a day before, and on the morning of the prayer. In addition, daily PM 2.5 concentrations were measured. Number concentrations in 0.5-1.0, 1.0-5.0, and>5.0μm diameter size ranges were monitored. In all campaigns the maximum number concentrations were observed on the most crowded days. The lowest number concentrations occurred when vacuuming was performed a day before the prayer day in two of the three size ranges considered. PM 2.5 concentrations (four-hour samples that integrated before, during, and after the prayer) were comparable to the other indoor environments reported in the literature. CO 2 concentrations suggested that ventilation was not sufficient in the mosque during the prayers. The results showed that better ventilation, a preventive cleaning strategy, and a more detailed study are needed.Article Citation - WoS: 303Citation - Scopus: 336A Health Risk Assessment for Exposure To Trace Metals Via Drinking Water Ingestion Pathway(Elsevier Ltd., 2009) Kavcar, Pınar; Sofuoğlu, Aysun; Sofuoğlu, Sait CemilA health risk assessment was conducted for exposure to trace metals via drinking water ingestion pathway for Province of İzmir, Turkey. Concentrations of 11 trace metals were measured in drinking waters collected from 100 population weighted random sampling units (houses). The samples were analyzed in atomic absorption spectrometry for arsenic, and inductively coupled plasma-optical emission spectrometry for Be, Cd, Co, Cr, Cu, Mn, Ni, Pb, V, and Zn. Questionnaires were administered to a participant from each sampling unit to determine drinking water consumption related information and demographics. Exposure and risks were estimated for each individual by direct calculation, and for İzmir population by Monte Carlo simulation. Six trace metals (As, Cr, Cu, Mn, Ni, and Zn) were detected in >50% of the samples. Concentrations of As and Ni exceeded the corresponding standards in 20% and 58% of the samples, respectively. As a result, arsenic noncarcinogenic risks were higher than the level of concern for 19% of the population, whereas carcinogenic risks were >10-4 for 46%, and >10-6 for 90% of the population.