Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 20Citation - Scopus: 21Long Term Stability of Biodegradable Polymers on Building Limestone(Elsevier Ltd., 2019) Kaplan, Zişan; Böke, Hasan; Sofuoğlu, Aysun; İpekoğlu, BaşakSynthetic polymers can be replaced by biodegradable ones as adhesives, water repellents and consolidants on the stone surfaces and facades of the historic buildings in their conservation to minimize future deterioration. In this study, the long-term stability of two biodegradable polymers, polyhydroxybutyrate (PHB) and poly-L-lactide (PLA), and an acrylic polymer (Paraloid B72) which is commonly used in conservation works of artefacts, were evaluated on limestone using a UV lamp-weathering chamber (up to 104 days) for future protection studies. Chemical and morphological changes induced by an accelerated weathering test were examined by Fourier Transform Infrared spectroscopy (FT-IR) and Scanning Electron Microscopy (SEM) analyses. Protection efficiency of the polymers was determined by the changes in color, capillary water absorption, static contact angle on limestone. Paraloid B72, PHB, and PLA coatings significantly increased hydrophobicity while decreasing capillarity water absorption and caused negligible change in the color of the limestone. Protection efficiencies of PLA and PHB polymers were almost the same as that of Paraloid B72, a widely used acrylic polymer. However, PLA and PHB seemed to be favorable polymers as protective agents due to their reversibility and biodegradability, low chromatic changes, good hydrophobic behavior and good stability to weathering in reducing the effects of outdoor exposure on limestone surfaces.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: 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: 8Citation - Scopus: 9Indoor Air Quality in Chemical Laboratories(Elsevier Ltd., 2016) Ugranlı, Tuğba; Güngörmüş, Elif; Sofuoğlu, Aysun; Sofuoğlu, Sait CemilChemical laboratories are special microenvironments, in which many pollutants may be found because of the large range and number of chemicals that can be used, while concentrations of some specific ones may relatively be elevated due to high source strengths depending on the type and the number of experiments conducted and the number of people working in the laboratory. Laboratories can be considered as public places for the students whereas they are occupational microenvironments for their staff (technicians, specialists and teaching/research assistants). Hence, laboratory indoor air quality (IAQ) is of importance due to chronic, toxic and carcinogenic health risks for the staff in addition to possible acute effects for both staff and students. This chapter presents background information regarding pertinent indoor air pollutants, factors that determine their concentrations, indoor environmental comfort, a review of the literature on indoor environmental quality in chemical laboratories and measures of IAQ management.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: 68Citation - Scopus: 75Air-Water Exchange of Polychlorinated Biphenyls (pcbs) and Organochlorine Pesticides (ocps) at a Coastal Site in Izmir Bay, Turkey(Elsevier Ltd., 2008) Odabaşı, Mustafa; Çetin, Banu; Demircioğlu, Eylem; Sofuoğlu, AysunThe air-water exchange of polychlorinated biphenyl (PCB) and organochlorine pesticides (OCPs) were investigated using paired air-water samples (n = 16) collected in July and February-March, 2005 from Guzelyali Port in Izmir Bay, Turkey. Atmospheric PCBs and OCPs were mainly in gas-phase in both periods. However, their dissolved and particle-phase water concentrations were comparable. For PCBs, 3 and 4-Cl congeners were dominant while chlorpyrifos, endosulfans and HCHs were the most abundant OCPs for all samples. Especially in summer, calculated net gas-exchange PCB fluxes were mainly volatilization from the water ranging from - 0.2 (volatilization, PCB-101) to - 30.0 (volatilization, PCB-31) ng m- 2 day- 1. For OCPs, net flux ranged from - 0.03 (volatilization, cis-nonachlor) to 1568 (deposition, endosulfan I) ng m- 2 day- 1 and they have seasonal variations with generally deposition in winter and volatilization in summer. However, endosulfan I, II, endosulfan sulfate, α- and γ-HCH deposited in both periods. The calculated residence times of PCBs and OCPs in the water column indicated that the gas-exchange in the Bay is at least as or a more important mechanism than advection. Annual gaseous absorption and volatilization fluxes were calculated and were used along with the estimated dry deposition fluxes and wet deposition fluxes measured recently at a suburban site in Izmir to determine the relative contributions of different atmospheric mechanisms to the pollutant inventory of the Bay water column. Results suggested that the relative contributions of all studied mechanisms to the water column PCB and OCP inventories were significant.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: 50Citation - Scopus: 55Determination 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, MustafaThe 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 Citation - WoS: 220Citation - Scopus: 234Determination of Octanol-Air Partition Coefficients and Supercooled Liquid Vapor Pressures of Pahs as a Function of Temperature: Application To Gas-Particle Partitioning in an Urban Atmosphere(Elsevier Ltd., 2006) Odabaşı, Mustafa; Çetin, Eylem; Sofuoğlu, AysunOctanol-air partition coefficients (KOA) for 14 polycyclic aromatic hydrocarbons (PAHs) were determined as a function of temperature using the gas chromatographic retention time method. log KOA values at 25° ranged over six orders of magnitude, between 6.34 (acenaphthylene) and 12.59 (dibenz[a,h]anthracene). The determined KOA values were within factor of 0.7 (dibenz[a,h]anthracene) to 15.1 (benz[a]anthracene) of values calculated as the ratio of octanol-water partition coefficient to dimensionless Henry's law constant. Supercooled liquid vapor pressures (PL) of 13 PAHs were also determined using the gas chromatographic retention time technique. Activity coefficients in octanol calculated using KOA and PL ranged between 3.2 and 6.2 indicating near-ideal solution behavior. Atmospheric concentrations measured in this study in Izmir, Turkey were used to investigate the partitioning of PAHs between particle and gas-phases. Experimental gas-particle partition coefficients (Kp) were compared to the predictions of KOA absorption and KSA (soot-air partition coefficient) models. Octanol-based absorptive partitioning model predicted lower partition coefficients especially for relatively volatile PAHs. Ratios of measured/modeled partition coefficients ranged between 1.1 and 15.5 (4.5±6.0, average±SD) for KOA model. KSA model predictions were relatively better and measured to modeled ratios ranged between 0.6 and 5.6 (2.3±2.7, average±SD).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, MustafaThe 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):