WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7150
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Article Kinetics of Proton Transfer in the Zeolitic Tuff(Central European Science Journals, 2009) Çakıcıoğlu Özkan, Seher Fehime; Özkan, Seher Fehime; Polatoğlu, İlkerThe kinetics of a proton transfer into dilute acid solutions containing natural zeolitic tuff was studied by following the pH evolution of the liquid phase. Four different solutions with tuff contents of 9, 3, 1 and 0.5 (% wt) and three different particle size fractions (≤ 2000 μm) were studied. The proton concentration of the solution was decreased by increasing the zeolite amount and decreasing the particle size fraction. The proton transfer reaction was analyzed with chemical reactions and diffusion model equations. Analysis shows that the adsorption and/or ion exchange are possible mechanisms and are expressed by a second order reaction model.Article Citation - WoS: 10Citation - Scopus: 10Clinoptilolite-Rich Mineral as a Novel Carrier for the Active Constituents Present in Ginkgo Biloba Leaf Extract(Elsevier Ltd., 2008) Göktaş, Selda; Ülkü, Semra; Bayraktar, OğuzThe possible use of clinoptilolite-rich mineral as a novel carrier for the active constituents present in Ginkgo biloba leaf extract solutions was investigated. The flavonoid aglycone constituents were found to be selectively adsorbed on the clinoptilolite surface. The antioxidant activity determinations of the extract solutions were performed by the Trolox Equivalent Antioxidant Capacity (TEAC) assay. The antioxidant activity measurements performed for the Ginkgo leaf extract solutions showed decreasing antioxidant activities due to adsorption. The decrease in antioxidant activity was attributed to the adsorption of phenolic constituents on the clinoptilolite surface.Article Citation - WoS: 29Citation - Scopus: 31Cure Kinetics of Epoxy Resin-Natural Zeolite Composites(Springer Verlag, 2008) Cansever Erdoğan, Beyhan; Seyhan, Abdullah Tuğrul; Ocak, Yılmaz; Tanoğlu, Metin; Balköse, Devrim; Ülkü, SemraThe cure kinetics of epoxy resin and epoxy resin containing 10 mass% of natural zeolite were investigated using differential scanning calorimetry (DSC). The conformity of the cure kinetic data of epoxy and epoxy-zeolite system was checked with the auto-catalytic cure rate model. The results indicated that the hydroxyl group on the zeolite surface played a significant role in the autocatalytic reaction mechanism. This group was able to form a new transition state between anhydride hardener and epoxide group. The natural zeolite particles acted as catalyst for the epoxy system by promoting its curing rate.Article Citation - WoS: 12Citation - Scopus: 17Diffusion Mechanism of Water Vapour in a Zeolitic Tuff Rich in Clinoptilolite(Springer Verlag, 2008) Çakıcıoğlu Özkan, Seher Fehime; Ülkü, SemraThe adsorption kinetics of H2O in a clinoptilolite rich zeolitic tuff was experimentally investigated at 18°C. In the identification of the diffusion mechanism the isothermal adsorption model equation was used. It was found out that the intraparticle mass transfer becomes more dominant over the heat transfer with increase in particle size and the adsorptive dose pressure. Although initially intraparticle mass transfer was the controlling resistance later external heat transfer also contributes to the transfer mechanism.Article Citation - WoS: 19Citation - Scopus: 21Microwave Effect on Ion-Exchange and Structure of Clinoptilolite(Springer Verlag, 2007) Akdeniz, Yelda; Ülkü, SemraThe effect of microwave irradiation on the ion exchange degree and structure of clinoptilolite mineral has been examined in comparison with the conventional heat treatment in waterbath. Clinoptilolite-rich mineral from the Western Anatolia, Bigadiç region was used for the experimental study. The mineral was mainly clinoptilolite (80-85%) and additionally, quartz (5-10%), and analcime+mordenite (<5%) were found as co-existing minerals. The mineral was stable towards dehydration and maintains its original structure up to 800°C. The BET and Langmuir surface areas of the sample were found to be 22 and 17m2/g for N2 adsorption and 28 and 22m2/g for Ar adsorption, respectively. For the exchange experiments, clinoptilolite rich mineral was treated with 1N NaCl salt solution both in a microwave unit and waterbath for 10min, 1h and 2h at 80°C. The waterbath treatment with the same conditions was continued for two additional weeks. The chemical composition of the parent and Na-exchanged forms of the clinoptilolite rich minerals were analyzed by using Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES). Microwave treatment was found to be more rapid and effective for ion exchange compared to conventional waterbath treatment. Additionally, the XRD results reveal that microwave irradiation has zero effect on the structure of the clinoptilolite rich mineral.Article Citation - WoS: 19Citation - Scopus: 21Kinetic and Thermodynamic Investigations of Strontium Ions Retention by Natural Kaolinite and Clinoptilolite Minerals(Walter De Gruyter Gmbh, 2005) Akar, Dilek; Shahwan, Talal; Eroğlu, Ahmet EminThe current study was devoted to the determination of various thermodynamic and kinetic parameters resulting from the fixation of Sr2+ by natural samples of kaolinite and clinoptilolite minerals. The sorption process followed pseudo second order kinetics, with faster sorption on kaolinite compared to clinoptilolite, where the uptake is affected by intraparticle diffusion. Freundlich and Dubinin-Radushkevich isotherm models described the data more adequately than Langmuir model, and clinoptilolite showed a higher strontium sorption capacity than kaolinite. Thermodynamically, the activation energy of Sr2+ sorption by kaolinite and clinoptilolite were respectively, -8.5 and -18.4 kJ/mol. The sorption process on both minerals was spontaneous and endothermic at all the studied concentrations, with ΔH° being 11.3 and 9.8 kJ/mol, for sorption on kaolinite and clinoptilolite, respectively. The findings of this study were compared with those of an earlier study on the uptake of Cs+ by the same minerals.Article Citation - WoS: 112Citation - Scopus: 130The Effect of Hcl Treatment on Water Vapor Adsorption Characteristics of Clinoptilolite Rich Natural Zeolite(Elsevier Ltd., 2005) Çakıcıoğlu Özkan, Fehime; Ülkü, SemraIn this study, water vapor adsorption properties of the clinoptilolite rich zeolite tuff, from Bigadic (Turkey), and its modified forms were examined. The modified forms were obtained by treating the tuff with HCl solutions (0.032, 0.16, 0.32, 1.6 or 5 M) at 25,40,75 and 100°C for 3 h. Infrared spectroscppy and water vapor adsorption were used for the characterization of the zeolites. Langmuir, BET and Dubinin-Raduschevich methods were applied in the analysis of water vapor adsorption data. Applications of Dubinin Raduschevich equation to the water adsorption data displayed that the super-micropore volume was not very sensitive to acid treatment. It was found out that the Langmuir surface area and ultra-micropore volume depend on the degree of the removal of aluminum from the structure.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.Article Citation - WoS: 50Citation - Scopus: 54Isomerization of ?-Pinene Over Calcined Natural Zeolites(Elsevier Ltd., 2004) Akpolat, Oğuz; Gündüz, Gönül; Özkan, Fehime; Beşün, NurgünIn this work, isomerization reaction of α-pinene was studied over several heat-treated natural zeolite catalysts, rich in clinoptilolite, from Balýkesir-Bigadic region in Turkey in a batch slurry reactor under nitrogen atmosphere. Zeolite samples were calcined at different temperatures such as 300, 450 and 600°C. All catalysts were tested in the isomerization reaction of α-pinene and were characterised by nitrogen adsorption experiments, IR, and XRD measurements. Acidity strength and the distribution of Lewis and Bronsted acid sites of the samples were determined. Selectivities to main reaction products, camphene and limonene, and reaction kinetics were investigated. Catalytic activity, that is total conversion of α-pinene, of heat-treated samples decreased with increasing calcination temperatures. Selectivity to limonene is dependent on α-pinene conversion at high conversion levels while the selectivity to camphene is not. The formation of heavy products increased with treatment temperature. It was seen that α-pinene consumption could be described by a first-order kinetics.Article Citation - WoS: 249Citation - Scopus: 268Silver, Zinc, and Copper Exchange in a Na-Clinoptilolite and Resulting Effect on Antibacterial Activity(Elsevier Ltd., 2004) Top, Ayben; Ülkü, SemraAg+-Na+, Zn2+-Na+, and Cu2+-Na+ equilibria for clinoptilolite-rich mineral from Gördes (Western Anatolia) were investigated at 25 °C and 0.1 N total solution normality. While silver exchange was favorable over the whole concentration range, zinc and copper were partially exchanged and preferred only at low concentrations. The standard free energies of exchanges for Ag+-Na+, Zn2+-Na+, and Cu2+-Na+ pairs were found as -6.0, 2.03, and 3.09 kJ/equiv., respectively. From these values, selectivity sequence was determined as Ag+>Na+ >Zn2+>Cu2+. Antibacterial activities of the exchanged samples were measured as a function of exchange level against Pseudomonas aeruginosa and Escherichia coli. Considering the selectivity sequence of the clinoptilolite and antibacterial activity results, Ag-clinoptilolite seemed to be promising antibacterial material.