Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 1Citation - Scopus: 1Exposure To Fumes of a Vegetable Margarine for Frying: Respiratory Effects in an Experimental Model(American Chemical Society, 2023) Cimrin, Arif H.; Alpaydin, Aylin Ozgen; Ozbal, Seda; Toprak, Melis; Yılmaz, Osman; Uluorman, Funda; Ergur, Bekir Uğur; Gürel, Duygu; Sofuoğlu, Sait CemilDeep frying is one of the strongest emission sources into indoor air. A vegetable margarine has recently been used in commercial kitchens. This study investigated the respiratory effects of exposure to its fumes in an experimental model. A setup with glass chambers was constructed. A chamber housed a fryer. The fumes were transported to the other chamber where 24 Wistar albino rats were placed in four randomized groups: acute, subacute, chronic, and control for the exposure durations. PM10 concentration in the exposure chamber was monitored to ensure occupational levels were obtained. Sacrification was performed 24 h after exposure. Lung, trachea, and nasal concha specimens were evaluated by two blinded histologists under a light microscope with hematoxylin–eosin. Mild mononuclear cell infiltration, alveolar capillary membrane thickening, alveolar edema, and diffuse alveolar damage, along with diffuse hemorrhage, edema, and vascular congestion in the interstitium were observed in the acute and subacute groups, and were overexpressed in the chronic group, whereas normal lung histology was observed in the control group. The results indicate that exposure to fumes of vegetable margarine for frying in commercial kitchens may cause pulmonary inflammation that becomes severe as the duration of the exposure increases.Book Part The Role of Polyurethane Foam Indoors in the Fate of Flame Retardants and Other Semivolatile Organic Compounds(American Chemical Society, 2021) Genişoğlu, Mesut; Sofuoğlu, Sait Cemil; Sofuoğlu, AysunFlame retardant chemicals are added to polyurethane foams (PUFs) during production. These chemicals are released to the environment during the use of PUF containing furniture or building materials. In contrast, organic pollutants such as polychlorinated biphenyls, polycyclic aromatic hydrocarbons, synthetic musk compounds, and volatile organic compounds could be sorbed by PUF depending on the concentration gradient, ambient temperature, and the physicochemical properties. Most of these substances tend to accumulate by adhering to organic matter in dust, particles, and surfaces, as they do not degrade for long periods of time. Sorption-emission cycles of PUF-associated organic compounds prolong their presence in indoor environments, which could increase human exposure. Since these organic compounds might have carcinogenic or chronic-toxic health effects on living organisms, it is important to understand the role of PUF in exposure to these substances in indoor environments. This chapter reviews the literature on the relationship of organic substances with PUF in indoor environments.Article Citation - WoS: 27Citation - Scopus: 28Fast Formation of Nitro-Pahs in the Marine Atmosphere Constrained in a Regional-Scale Lagrangian Field Experiment(American Chemical Society, 2019) Mulder, Marie D.; Dumanoğlu, Yetkin; Efstathiou, Christos; Kukucka, Petr; Matejovicova, Jana; Maurer, Christian; Pribylova, Petra; Prokes, Roman; Sofuoğlu, Aysun; Sofuoğlu, Sait Cemil; Wilson, Jake; Zetzsch, Cornelius; Wotawa, Gerhard; Lammel, GerhardPolycyclic aromatic hydrocarbons (PAHs) and some of their nitrated derivatives, NPAHs, are seemingly ubiquitous in the atmospheric environment. Atmospheric lifetimes may nevertheless vary within a wide range, and be as short as a few hours. The sources and sinks of NPAH in the atmosphere are not well understood. With a Lagrangian field experiment and modeling, we studied the conversion of the semivolatile PAHs fluoranthene and pyrene into the 2-nitro derivatives 2-nitrofluoranthene and 2-nitropyrene in a cloud-free marine atmosphere on the time scale of hours to 1 day between a coastal and an island site. Chemistry and transport during several episodes was simulated by a Lagrangian box model i.e., a box model coupled to a Lagrangian particle dispersion model, FLEXPART-WRF. It is found that the chemical kinetic data do capture photochemical degradation of the 4-ring PAHs under ambient conditions on the time scale of hours to 1 day, while the production of the corresponding NPAH, which sustained 2-nitrofluoranthene/fluoranthene and 2-nitropyrene/pyrene yields of (3.7 ± 0.2) and (1.5 ± 0.1)%, respectively, is by far underestimated. Predicted levels of NPAH come close to observed ones, when kinetic data describing the reactivity of the OH-adduct were explored by means of theoretically based estimates. Predictions are also underestimated by 1-2 orders of magnitude, when NPAH/PAH yields reported from laboratory experiments conducted under high NOx conditions are adopted for the simulations. It is concluded that NPAH sources effective under low NOx conditions, are largely underestimated.Article Citation - WoS: 49Citation - Scopus: 52Evaluation of a Conceptual Model for Gas-Particle Partitioning of Polycyclic Aromatic Hydrocarbons Using Polyparameter Linear Free Energy Relationships(American Chemical Society, 2016) Shahpoury, Pourya; Lammel, Gerhard; Albinet, Alexandre; Sofuoglu, Aysun; Dumanoğlu, Yetkin; Sofuoğlu, Sait Cemil; Wagner, Zdenek; Zdimal, VladimírA model for gas-particle partitioning of polycyclic aromatic hydrocarbons (PAHs) was evaluated using polyparameter linear free energy relationships (ppLFERs) following a multiphase aerosol scenario. The model differentiates between various organic (i.e., liquid water-soluble (WS)/organic soluble (OS) organic matter (OM), and solid/semisolid organic polymers) and inorganic phases of the particulate matter (PM). Dimethyl sulfoxide and polyurethane were assigned as surrogates to simulate absorption into the above-mentioned organic phases, respectively, whereas soot, ammonium sulfate, and ammonium chloride simulated adsorption processes onto PM. The model was tested for gas and PM samples collected from urban and nonurban sites in Europe and the Mediterranean, and the output was compared with those calculated using single-parameter linear free energy relationship (spLFER) models, namely Junge-Pankow, Finizio, and Dachs-Eisenreich. The ppLFER model on average predicted 96 ± 3% of the observed partitioning constants for semivolatile PAHs, fluoranthene, and pyrene, within 1 order of magnitude accuracy with root-mean-square errors (RMSE) of 0.35-0.59 across the sites. This was a substantial improvement compared to Finizio and Dachs-Eisenreich models (37 ± 17 and 46 ± 18% and RMSE of 1.03-1.40 and 0.94-1.36, respectively). The Junge-Pankow model performed better among spLFERs but at the same time showed an overall tendency for overestimating the partitioning constants. The ppLFER model demonstrated the best overall performance without indicating a substantial intersite variability. The ppLFER analysis with the parametrization applied in this study suggests that the absorption into WSOSOM could dominate the overall partitioning process, while adsorption onto salts could be neglected. (Figure Presented).Article Citation - WoS: 68Dry Deposition Fluxes and Mass Size Distributions of Pb, Cu, and Zn Measured in Southern Lake Michigan During Aeolos(American Chemical Society, 1998) Paode, Rajendra D.; Sofuoğlu, Sait Cemil; Sivadechathep, Jakkris; Noll, Kenneth E.; Holsen, Thomas M.; Keeler, Gerald J.As part of the Atmospheric Exchange Over Lakes and Oceans Study (AEOLOS) the dry deposition fluxes and atmospheric size distributions (ASDs) of anthropogenic metals were measured over the southern basin of Lake Michigan. The measurements were made during winter, summer, and fall, concurrently, in Chicago, IL; over Lake Michigan onboard the U.S. EPA RV Lake Guardian; and in South Haven, MI. The flux of Pb, Cu, and Zn was substantially higher in Chicago than in either South Haven or over Lake Michigan. The average measured Pb, Cu, and Zn fluxes were 0.07, 0.06, and 0.20 mg m-2 day-1 in Chicago; 0.003, 0.01, and 0.01 mg m-2 day-1 over Lake Michigan; and 0.004, 0.007, and 0.004 mg m-2 day-1 in South Haven. When the wind was from Chicago over the lake, the fluxes and concentrations measured over the lake were higher than when the wind was from other directions. In general, these anthropogenic metals had higher concentrations in the fine particle mode than in the coarse particle mode. Modeled and measured fluxes were in reasonable agreement. Coarse particles were found to be responsible for the majority of the flux at all locations.