Environmental Engineering / Çevre Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/4321
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Article Citation - WoS: 6Citation - Scopus: 9The Effect of Military Conflict Zone in the Middle East on Atmospheric Persistent Organic Pollutant Contamination in Its North(Elsevier, 2023) Ayrı, İlknur; Genişoğlu, Mesut; Sofuoğlu, Aysun; Kurt Karakuş, Perihan B.; Birgül, Askın; Sofuoğlu, Sait CemilThis study aimed to investigate long-range atmospheric transport of selected POPs released due to the effects of mili-tary conflicts in regions to the south of Turkey's borders. Ten locations were selected to deploy passive air samplers at varying distances to the border on a southeast-west transect of the country, proximity-grouped as close, middle, and far. Sampling campaign included winter and transition months when desert dust transport events occur. Hypothesis of the study was that a decreasing trend would be observed with increasing distance to the border. Group comparisons based on statistical testing showed that PBDE-183, E45PCB, and dieldrin in winter; PBDE-28, PBDE-99, PBDE-154, p,p '-DDE, E14PBDE, and E25OCP in the transition period; and PBDE-28, PBDE-85, PBDE-99, PBDE-154, PBDE-190, PCB-52, E45PCB, p,p '-DDE, and E25OCP over the whole campaign had a decreasing trend on the transect. An analysis of concen-tration ratio to the background showed that long-range atmospheric transport impacted the study sites, especially those of close group in comparison to the local sources. Back-trajectory analyses indicated that there was transport from the conflict areas to sites in the close-proximity group, while farther sampling locations mostly received air masses from Europe, Russia, and former Soviet Union countries, followed by North Africa, rather than the military con-flict areas. In consequence, decrease in concentrations with distance and its relation to molecular weight through pro-portions, diagnostic ratios, analysis of concentration ratio to the background, and back-trajectory analyses support the effect of transport from the military-conflict area to its north.Article Citation - WoS: 3Citation - Scopus: 6Halogenated By-Products in Chlorinated Indoor Swimming Pools: a Long-Term Monitoring and Empirical Modeling Study(Amer Chemical Soc, 2023) Genişoğlu, Mesut; Minaz, Mert; Tanacan, Ertaç; Sofuoğlu, Sait Cemil; Kaplan-Bekaroğlu, Şehnaz Şule; Kanan, Amer; Ateş, NurayMonitoring the disinfection process and swimming pool water quality is essential for the prevention of microbial infections and associated diseases. However, carcinogenic and chronic-toxic disinfection by-products (DBPs) are formed with reactions between disinfectants and organic/inorganic matters. DBP precursors in swimming pools originate from anthropogenic sources (body secretions, personal care products, pharmaceuticals, etc.) or chemicals used in pools. Temporal (48 weeks) water quality trends of trihalomethanes (THMs), haloacetic acids (HAAs), haloacetonitriles (HANs), and halonitromethanes (HNMs) in two swimming pools (SP-A and SP-B) and precursor-DBP relationships were investigated in this study. Weekly samples were taken from swimming pools, and several physical/chemical water quality parameters, absorbable organic halides (AOX), and DBPs were determined. THMs and HAAs were the most detected DBP groups in pool water. While chloroform was determined to be the dominant THM compound, dichloroacetic acid and trichloroacetic acid were the dominant HAA compounds. The average AOX concentrations were measured to be 304 and 746 mu g/L as Cl- in SP-A and SP-B, respectively. Although the amount of AOX from unknown chlorinated by-products in SP-A did not vary temporally, a significant increase in unknown DBP concentrations in SP-B was observed over time. AOX concentrations of chlorinated pool waters were determined to be an important parameter that can be used to estimate DBP concentrations.Article Citation - WoS: 26Citation - Scopus: 26Multi-Route - Multi-Pathway Exposure To Trihalomethanes and Associated Cumulative Health Risks With Response and Dose Addition(Academic Press Inc., 2019) Genişoğlu, Mesut; Ergi Kaytmaz, Ceyda; Sofuoğlu, Sait CemilCumulative health risk estimation for exposure to mixtures is a current issue, which would present a useful tool for environmental and public health management. Cumulative risks were estimated with response and dose addition methods for individual multi-route - multi-pathway exposure to trihalomethanes and associated carcinogenic toxic risks in Izmir, Turkey. Exposure levels were estimated for ingestion, dermal, and inhalation routes using measured tap water and bottled water THM concentrations. Drinking, showering, hand and dish washing were the considered pathways. THM concentrations in air during the showering were modeled with two-resistance theory using tap water concentration data. The estimated carcinogenic risk levels for ingestion route were in the range of safe (< 10(-6)) to low priority (< 10(-4)), for dermal route all were in the safe zone (< 10(-6)), and for inhalation route were in the range of safe to high priority (> 10(-4)) zones, indicating ingestion and inhalation routes were of similar significance ahead of dermal exposure. Cumulative carcinogenic risks of THM compounds were estimated using simple (response) addition and dose addition using cumulative relative potency factor (CRPF) methods. CRPF method estimated the risks at lower levels compared to the simple addition, which originated from the use two different risk factor values for the index chemical in the method. Cumulative chronic-toxic risks were also assessed, rendering below the threshold risk levels for all routes. This study showed that multi-route - multi-pathway exposure assessment and cumulative risk assessment should together be considered for better environmental and public health management.Article Citation - WoS: 20Citation - Scopus: 25Indoor Air Partitioning of Synthetic Musk Compounds: Gas, Particulate Matter, House Dust, and Window Film(Elsevier, 2020) Balcı, Esin; Genişoğlu, Mesut; Sofuoğlu, Sait Cemil; Sofuoğlu, AysunDue to diversity of contaminants indoors and complexity in the physical structure of particulate matter, partition process of chemicals affects indoor concentration distribution. Synthetic Musk Compounds (SMCs) are ubiquitously found in household and personal care products, thus, in the environment. Exposure to SMCs is important for human health, therefore, their partitioning in indoor environmental media is a key issue. In this study, gas particle, house dust, andwindowfilm partitioning of SMCs were investigated in an indoor micro-environment. In a sealed and unoccupied room, a polycyclic and nitro musk mixture was left for volatilization for an hour. Then, samples were collected using XAD-2 sandwiched between two PUF plugs, glass-fiber filter, and wipes for gas, PM10, window-film, house dust phases, respectively, for 145 h. Collected samples were analyzed using a GC-MS. Results demonstrated that MC concentrations decreased over time, non-linearly. Six of the SMCs partitioned to PM10 with at least 10% at beginning of the experiment, whereas the number of compounds dropped to two at the end, showing that SMCs may partition well between the two phases but they tend to be in the gas phase. They were also detected in the film and dust phases but a decrease pattern similar to gas-particle was not observed. Spearman correlations indicate that the dust and film-associated concentrations were governed by similar processes but PM-associated concentrations were not. SMCs may be found in all phases, mainly in house dust in terms of mass among the studied media and unaccounted surface reservoirs. Therefore, their partitioning between indoor media has key implications for human exposure. (C)20 Elsevier B.V. All rights reserved.Article Citation - WoS: 5Citation - Scopus: 7Bleach-Containing Automatic Toilet-Bowl Cleaners as Sources of Vocs, Associated Indoor Air Concentrations and Carcinogenic Risk(Turkish National Committee for Air Pollution Research (TUNCAP), 2020) Ayrı, İlknur; Genişoğlu, Mesut; Gaygısız, Handan; Sofuoğlu, Aysun; Sofuoğlu, Sait CemilHousehold cleaning products are sources of volatile organic compounds (VOCs). Bleach containing products are a special case because reactions occur between chloride and their organic content such as surfactants, perfumes, etc., generating VOCs. This study aimed to determine concentration of 13 VOCs in bleach-containing automatic toilet cleaners, to estimate their indoor air concentrations and associated exposure and health risk levels. Experiments with products purchased from supermarkets were conducted in 20-mL headspace vials by placing 1 g of sample with and without water. Solid-phase micro extraction with a DVB/CAR/PDMS fiber assembly was used for adsorption of VOCs from the headspace, and analyzed using a GC-MS. The median carbon tetrachloride and chloroform concentrations of the studied products ranged from 5.03 × 10?3 to 2.37 × 10?2 ?g/g and 2.53 × 10?2 to 2.37 ?g/g, respectively. The modeled 95th percentile indoor air concentrations in a 1.6 m3 bathroom with no ventilation were estimated to be 1 and 20 ?g/m3 for carbon tetrachloride and chloroform, respectively. The 95th percentile carcinogenic risk associated even with the use of the highest content product, 3.72 × 10?7 and 8.62 × 10?7 for carbon tetrachloride and chloroform respectively, were below the acceptable risk. In conclusion, automatic toilet-bowl cleaners were found to be sources of VOCs, but their emission potentials are not high to cause considerable indoor air concentrations over their suggested product lifetime. In turn, carcinogenic risks associated with inhalation exposure are below the de Minimis risk level of 10?6. © 2020Article 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: 3Citation - Scopus: 4Use of Nano Zero-Valent Iron Coated Coffee Grounds for Removal of Zn(ii) and Ni(ii) From Aqueous Solutions(Desalination Publications, 2019) Gören, Ayşegül Yağmur; Genişoğlu, Mesut; Ökten, Hatice EserThis research investigates the adsorption capacity of a novel composite material, namely nano zero-valent iron coated coffee grounds (nZVI-CG), for removal of zinc (Zn) and nickel (Ni). nZVI particles were synthesized and immobilized to the surface of waste coffee grounds (CG) using the ultrasonic-assisted liquid phase method. Characterization of synthesized nZVI-CG composite and bare CG showed that nZVI coating has increased the surface area significantly. Batch tests were conducted to examine the effects of pH, reaction time and initial metal concentrations on Zn2+ and Ni2+ removal. At an initial metal concentration of 10 mg-Ni/L and 10 mg-Zn/L, nZVI-CG removal rates for Zn2+ and Ni2+ were observed as 98.89% and 97.29%, respectively; while removal rates of bare CG have remained at 51% (Zn2+) and 48.1% (Ni2+). Moreover, acidic conditions were observed to deteriorate Ni2+ and Zn2+ adsorption since most functional groups of the metals were protonated. Increasing initial nickel and zinc concentrations decreased removal rates. While the model fittings improved with increasing pH, in the case of nZVI-CG, Langmuir isotherm gave the best fits for Ni2+ and Zn2+ at pH 5 and 7. Also, our experimental results followed the pseudo-second-order kinetic model, regardless of the used adsorbent. Consequently, our results showed that nZVI-CG composite material is a promising alternative adsorbent for pilot scale metal removal/recovery applications.