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: 53Citation - Scopus: 60Supercritical Deposition of Pt on Sno2-Coated Al2o3 Foams: Phase Behaviour and Catalytic Performance(Elsevier Ltd., 2008) Garrido, G. Incera; Patcas, F. C.; Upper, G.; Türk, M.; Yılmaz, Selahattin; Kraushaar-Czarnetzki, B.Deposition and reduction of an organometallic platinum complex from a supercritical Pt(COD)Me2/CO2 solution was carried out to produce Pt/SnO2 catalysts supported on Al2O3 foams for CO oxidation at moderate temperatures. The phase behaviour of the complex in supercritical carbon dioxide was investigated to find the optimum pressure and temperature conditions for the deposition. For the Pt(COD)Me2/CO2 mixture, the melting point decreased with increasing pressure from 378 K at 0.1 MPa to 360 K at 25.6 MPa. Additional investigations showed that the solubility of Pt(COD)Me2 in CO2 increases from 5.9 × 10-4 mol/mol at 11.2 MPa and 313 K to 3.4 × 10-3 mol/mol at 29.6 MPa and 353 K. The supercritical deposition yielded catalysts with highly dispersed platinum nanoparticles of approx. 3 nm having a narrow size distribution and thus, a superior activity towards oxidation of carbon monoxide in comparison to a catalyst prepared by the conventional aqueous impregnation of Pt.Article Citation - WoS: 262Citation - Scopus: 286Dye Adsorption Behavior of Luffa Cylindrica Fibers(Elsevier Ltd., 2008) Demir, Hasan; Top, Ayben; Balköse, Devrim; Ülkü, SemraUsing natural Luffa cylindrica fibers as adsorbent removal of methylene blue dye from aqueous solutions at different temperatures and dye concentrations was investigated in this study. Thermodynamics and kinetics of adsorption were also investigated. The adsorption isotherms could be well defined with Langmuir model instead of Freundlich model. The thermodynamic parameters of methylene blue (MB) adsorption indicated that the adsorption is exothermic and spontaneous. The average MB adsorption capacity was found out as 49 mg/g and average BET surface area of fibers was calculated as 123 m2/g.Article Citation - WoS: 44Citation - Scopus: 54Protection of Marble Surfaces by Using Biodegradable Polymers as Coating Agent(Elsevier, 2009) Ocak, Yılmaz; Sofuoğlu, Aysun; Tıhmınlıoğlu, Funda; Böke, HasanBiodegradable polymers have been replaced over the synthetic polymers in many applications due to their good properties such as reversibility and biodegradability. Therefore they allow new treatment on the surface of the material to be protected and they fulfil the principles generally accepted by the International Conservation Community of Historic Monuments and Buildings. In this study, the efficiency of four different biodegradable polymers as protective coatings on marble-SO2 reaction was investigated. The polymers used were zein, chitosan, polyhydroxybutyrate (PHB), and poly-l-lactide (PLA). The mineralogical composition, bulk density and porosity of uncoated marble were determined. The water vapor permeability, water absorption by capillary forces, surface wettability, and color alteration of uncoated and coated marbles were measured. For sulphation reaction, marble slabs were coated with these polymers and then they were exposed at nearly 8 ppm SO2 concentration at 100% relative humidity conditions together with uncoated ones in a reaction chamber for several days for testing their protection efficiency. The extent of reaction was determined by leaching of gypsum formed on the marble surfaces in deionized water and then determining the sulphate content by ion chromatography. The protection efficiency of polymer treatments was expressed as comparing the gypsum crust thickness of the coated and uncoated marble plates. The comparison among the polymers showed that the surface hydrophobicity, water capillary absorption and structure of polymer would be important factors affecting the protection efficiency. The use of high molecular weight PLA (HMWPLA) polymer on marble surfaces provided significant protection up to 60% which was indicated that HMWPLA polymer seems to be promising polymer as protective coating agent in reducing gypsum formation on marble surfaces in the polluted environment.Article Citation - WoS: 14Citation - Scopus: 15Neutralization of an Extremely Acidic Sludge and Stabilization of Heavy Metals in Flyash Aggregates(Elsevier Ltd., 2007) Polat, Mehmet; Güler, Erkan; Lederman, Eli; Cohen, HaimAn extremely acidic, heavy metal-rich sludge (pH = -1.2) was scrubbed with a Class-F fly ash in order to simultaneously neutralize the acidity and stabilize the heavy metals contained in both wastes. This paper outlines the leaching behavior of the aggregate material generated by scrubbing. For proper fly ash/sludge ratios, the fly ash acted as an outstanding neutralizer for the acidic waste. Leaching of heavy metals from the aggregate samples was below the environmental limits within a pH range between 3 and 9. Subsequent washing of the leached aggregate with acidic CALWET solutions did not result in an additional release of heavy metals. It is proposed that coordinative bonding of the metal cations onto neutral surface sites and electrostatic adsorption led to stabilization of the heavy metals within the aggregate structure below hydrolysis pHs.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):Article Citation - WoS: 41Citation - Scopus: 43Isomerisation of ?-Pinene Over Beta Zeolites Synthesised by Different Methods(Elsevier Ltd., 2005) Gündüz, Gönül; Dimitrova, Raina D.; Yılmaz, Selahattin; Dimitrov, Ljubomir; Spassova, MayaLiquid-phase α-pinene isomerisation at l00°C in a batch reactor is studied over Beta zeolites synthesised by different methods. It is confirmed that α-pinene forms a carbenium ion in an acidic environment, which rearranges without capture by nucleophiles, to form mainly hydrocarbons as camphene, terpinenes, terpinolenes and heavy products. The microporous Beta samples show low activity despite the high acidity most probably because of the hindered intermediate formation. The nature of the enhanced activity of Beta mesopores samples is suggested to be a result from the high accessibility of the acidic sites. The isomerisation of α-pinene was studied over Beta zeolites synthesised by different methods. The main products are camphene, terpinenes, terpinolenes and heavy products. Beta zeolites with micro-/mesopores reveal excellent activity because of the appropriate balance between acidity and bimodal pore system. The microporous Beta samples show low activity despite the good total acidity most probably because of the steric effect for the formation of the intermediate cations.Article Citation - WoS: 36Citation - Scopus: 40The Kinetics of Citral Hydrogenation Over Pd Supported on Clinoptilolite Rich Natural Zeolite(Elsevier Ltd., 2005) Yılmaz, Selahattin; Uçar, Şule; Artok, Levent; Güleç, HilalThe liquid phase hydrogenation of citral has been investigated over Pd (2.42%) supported on clinoptilolite rich natural zeolite catalyst for different reaction conditions. The zeolite support did not affect the active metal properties. This was attributed to the large size of Pd particles on the support. High selectivity (90%) to citronellal was obtained at complete conversion of citral. The catalytic activity increased with reaction temperature (80, 100, 120°C) following an Arrhenius behaviour, while selectivity remained constant for a given conversion. Selectivity to citronellal increased from 78 to 90% with increase in the amount of catalyst in the reaction solution (Citral/Pd mole ratio 293, 176 and 105). The spent catalyst regained its fresh activity and selectivity upon regeneration.
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