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: 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: 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: 21Citation - Scopus: 26Indoor Environmental Quality in Chemistry and Chemical Engineering Laboratories at Izmir Institute of Technology(Turkish National Committee for Air Pollution Research (TUNCAP), 2015) Ugranlı, Tuğba; Toprak, Melis; Gürsoy, Gül; Çimrin, Arif H.; Sofuoğlu, Sait CemilIndoor air pollution in university research laboratories may be important to building occupants, especially for those who work in the laboratories. In this study, indoor air quality (IAQ) and indoor environmental comfort were investigated in research laboratories of two departments at a university. PM2.5, PM10, TVOC (total volatile organic compounds), and CO concentrations, and three comfort variables which are temperature, relative humidity, and CO2 were measured. PM2.5 concentration was determined gravimetrically by collecting particles on glass fiber filters, whereas the remaining pollutants and comfort variables were measured using a monitoring device. IAQ measurements showed that levels of all pollutants were under the limits in both of the departments except for TVOC in one laboratory which had a mean concentration of 182 ppb. The comfort variables were in the comfort ranges for laboratories in both of the departments except for temperature in one laboratory with a mean value of 30 °C. In conclusion, measures are needed for extensive uses of organic solvents because ventilation may not be sufficient to keep VOC concentrations within the limits, and to provide thermal comfort.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: 14Citation - Scopus: 15Chitosan-Immobilized Pumice for the Removal of As(v) From Waters(Springer Verlag, 2014) Turan, Dilek; Kocahakimoğlu, Cemre; Boyacı, Ezel; Sofuoğlu, Sait Cemil; Eroğlu, Ahmet EminA novel sorbent, chitosan-immobilized pumice, has been prepared for the sorption of As(V) from waters prior to its determination by hydride generation atomic absorption spectrometry. The success of the immobilization has been checked with such characterization techniques as scanning electron microscopy, thermal gravimetric analysis, and elemental analysis. Points of zero charge of the sorbents were determined with potentiometric mass titration. Batch-type equilibration studies have shown that the novel sorbent can be employed at a wide pH range resulting in quantitative sorption (>90 %) at pH 3.0-7.0 and greater than 70 % sorption at pH >8.0. These results demonstrate the advantage of immobilizing chitosan onto pumice, because, under the same conditions, pumice displays <20 % sorption toward As(V), whereas chitosan gives approximately 90%sorption only at pH 3.0. The validity of the method was verified through the analysis of ultrapure, bottled drinking, and tap water samples spiked with arsenate; the respective sorption percentages of 93.2 (±0.7), 89.0 (±1.0), and 80.9 (±1.3) were obtained by batch-type equilibration. Arsenic sorption was also examined in the presence of common interfering ions resulting in competing effects of PO3- 4 and NO- 3on As(V) adsorption.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: 21Citation - Scopus: 23Activated Carbon Adsorption of Fuel Oxygenates Mtbe and Etbe From Water(Springer Verlag, 2009) İnal, Fikret; Yetgin, Senem; Aksu, Gülsüm T.; Şimşek, Selvi; Sofuoğlu, Aysun; Sofuoğlu, Sait CemilThe aqueous phase adsorption of fuel oxygenates methyl tertiary butyl ether (MTBE) and ethyl tertiary butyl ether (ETBE) onto commercially available granular activated carbon (GAC; Norit GAC 1240) was investigated in a batch system at 27°C. The oxygenate concentrations were determined by headspace gas chromatography/mass spectrometry analyses. The experimental data were used with four two-parameter isotherm models (Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich) and two kinetic models (pseudo first-order and pseudo second-order) to determine equilibrium and kinetic parameters. Considering the correlation coefficient and root mean square error, Dubinin-Radushkevich isotherm showed better fit with the equilibrium data for MTBE. However, the performances of Langmuir and Dubinin-Radushkevich models were comparable for ETBE. The adsorption capacities were calculated as 5.50 and 6.92 mg/g for MTBE and ETBE, respectively, at an equilibrium solution concentration of 1 mg/L using Dubinin-Radushkevich isotherm. The differences between the model predictions and experimental data were similar for the pseudo first-order and pseudo second-order kinetic models. Gibbs free-energy changes of adsorption were found to be -22.59 and -28.55 kJ/mol for MTBE-GAC and ETBE-GAC systems, respectively, under the experimental conditions studied.