Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Conference Object Citation - Scopus: 1Yapay Sindirim Sıvısında Doğal Zeolitlerde Meydana Gelen Morfolojik Değişmeler(Institute of Electrical and Electronics Engineers Inc., 2009) Demirbüker Kavak, Dilek; Özçelik, Serdar; Ülkü, SemraDoğal zeolitler biyoaktif maddelerdir. Doğal zeolitlerin hayvanlarda biyokütle arttırıcı besi katkı maddesi, insanlarda ülser tedavisinde mide asitliğini tamponlayıcı, asitliği düşürücü ilaç gibi değişik kullanım alanları mevcuttur. Değişik sağlık alanlarında kullanımlarından dolayı, zeolitlerin yapısal stabilitesinin sindirim sırasında belirlenmesi; olası olumlu veya olumsuz etkileşimleri anlamak açısından önem taşımaktadır. Gerçekleştirilen araştırmada, yapay sindirim sırasında zeolitte meydana gelebilecek olası morfolojik değişimlerin incelenmesi hedeflenmiştir. Bu amaçla zeolitin ABTS ile radikal sönümleme kapasitesi araştırılmış, yapay sindirim denemeleri gerçekleştirilerek de uygulama süreci sonrası yapıda olası değişimler ve adsorpsiyonlar taramalı elektron mikroskobu, FTIR, XRD analizleri ile incelenmiştir. 3g/100ml zeolitin ABTS radikalini %45 inhibe ettiği bulunmuştur. Taramalı elektron mikroskobu deneyleri sonucunda yapay sindirilmiş örneklerin yüzey morfolojisinde değişim gözlenmemiştir. Element analizleri yapısal kaybın olmadığını, Al ve Si elementlerinin ağırlıkça yüzdelerinin, kontrol örnekleriyle (Al:8.1; Si: 39) sindirilmiş örneklerde (Al:8.2; Si: 38.3) yaklaşık aynı olduğunu göstermiştir. Infrared spektrum (IR) ve X-ray ışını kırınımı analizleri sonuçları ise bu bulguları doğrulamıştır. Ayrıca taramalı elektron mikroskobu ve IR spektrum sonuçları yapay sindirim ortamındaki maddelerin, zeolit yüzeyinde adsorplanmadıklarıını göstermektedir. Sonuç olarak doğal zeolitler, yapay sindirim sırasında yapısal stabilitelerini kaybetmemektedirler.Conference Object Citation - WoS: 4Citation - Scopus: 4Antioxidative and Antimicrobial Screening of 19 Commercial Essential Oils in Turkey(International Society for Horticultural Science, 2009) Bulut, Çisem; Altıok, Evren; Bayraktar, Oğuz; Ülkü, SemraPlant oils have been used for wide variety purposes for many years in Turkey. These essential oils have usage in many areas such as perfumery, cosmetic, food flavoring and folkloric medicine. In the study, 19 commercial essential oils were studied by means of antibacterial and antioxidant capacity. Antibacterial test was performed against S. aureus, S. epidermidis, K. pneumoniae and E. coli using standard disc diffusion method. Penicillin, gentamicin and vancomycin discs were also included. Inhibition zones (mm) were recorded to indicate antibacterial property. Penicillin (44 mm) and vancomycin (14 mm) could inhibit only S. aureus. Except essential oils of Juniperus nana (Ardiç), Ocimum basilicum (Feslegen), Urtica dioica (Isirgan), Foeniculum vulgare (Rezene) ressential oils indicated antimicrobial activity against some of the test microorganims. The most active essential oil was found as Thymus serpyllum (Kekik). It indicated highest inhibition zones for other microorganisms among others. Antioxidant capacities were measured using photochemiluminescence (PCL) method. The highest antioxidant activity was measured for Dianthus caryophyllus (Karanfil) as 547.781 103 ug trolox/mL of oil. It was followed by Thymus serpyllum (Kekik), Lilium candidum (Zambak) and Matricaria chamomilla (Papatya). Especially, Thymus serpyllum and Dianthus caryophyllus have significant antimicrobial and antioxidant capacity therefore it could be suggested for further investigations and applications.Article Citation - WoS: 2Citation - Scopus: 10Water and Water Vapor Sorption Studies in Poly(propylene)-Zeolite Composites(John Wiley and Sons Inc., 2003) Pehlivan, Hilal; Özmıhçı, Filiz; Tıhmınlıoğlu, Funda; Balköse, Devrim; Ülkü, SemraWater and water vapor sorption to porous poly(propylene)zeolite composites prepared by hot pressing have been studied as a function of zeolite loading. This work presents the first report on the effect of the zeolite as a filler on the water sorption properties of PP composites. Water swelling experiments were conducted at 25°C using pure PP and PP-zeolite film samples having different zeolite loadings (6-40 wt%). Since PP is a hydrophobic polymer, it does not sorp any water, but the composites having 10, 20, 30, and 40% zeolite sorbed 0.63, 1.00, 1.72 and 3.74 wt% water, respectively. The zeolite itself at the same conditions sorbed 24.5 wt% water. As the filler loading in the composites increased, equilibrium uptake values increased too. On the other hand, water vapor sorption and kinetics has been studied using a Cahn 2000 gravimetric sorption system. Within in the range 0.35-0.95%, water vapor was adsorbed by the composites containing 10-40 wt% zeolite. Experimental effective water vapor diffusivities of the composite films were about one order of magnitude higher than the experimental water diffusion coefficient in composites. The transport of water in composites was slower than that in the liquid water due to the longer diffusion pathway and adsorption on the surface of the composites. Although the liquid water may fill all the voids in the composite, water vapor is adsorbed on the surface of the zeolite only.Article Citation - WoS: 4Citation - Scopus: 5Dynamic Heat of Adsorption of Water Vapour on Zeolitic Tuff and Zeolite 4a by Flow Microcalorimetry(Scibulcom Ltd., 2006) Ülkü, Semra; Balköse, Devrim; Alp, BurcuIn this study a practical method for measurement of heat of adsorption of water vapour on adsorbents was developed to evaluate the feasibility of substitution of a zeolitic tuff with zeolite 4A in air drying and heat pumps. The change of heat of adsorption with inlet humidity of the air passing through the calorimeter was investigated. Samples were characterised by X-ray diffraction and thermal gravimetric analysis techniques. Specific heats of the zeolitic tuff and zeolite 4A were measured as 1.01 and 1.42 J/g K, respectively. Adsorption isotherms fitted to the Langmuir model with regression coefficient 0.93 and 0.94 with monolayer capacities, Xm 9.68% and 26.35% H 2O for the zeolitic tuff and zeolite 4A, respectively. The energy storage intensity was measured in the range 48-97 J/g and 464-201 J/g for the tuff and zeolite 4A, respectively. Heat of adsorption of zeolite decreased with surface coverage and it was in the range 1750-2835 and 1104-2640 J/g H 2O for the zeolitic tuff and zeolite 4A, respectively.Article Citation - WoS: 2Citation - Scopus: 2A Study of Chemical and Physical Changes During Biaxially Oriented Polypropylene Film Production(Walter de Gruyter GmbH, 2003) Ülkü, Semra; Balköse, Devrim; Arkış, Esen; Sipahioğlu, MuzafferPolypropylene films obtained during the biaxial orientation process were characterized by energy dispersive X-ray analysis (EDX), scanning electron microscopy. X-ray diffraction, differential scanning calorimetry, infrared spectroscopy. Inorganic particles with Al, Si, Na, Mg, Ti, K,O elements were present in biaxially oriented films. Polypropylene had molecules with both isotactic configuration and it was crystallized only in isotactic α phase. The films drawn in one and two directions had unit cells with b axis parallel to surface of the films. The antioxidants present in the films were consumed during processing, preventing polypropylene oxidation in air at high processing temperatures. One surface of the films contained less polypropylene and had functional groups rich in oxygen such as C=O and COO.Article Citation - WoS: 3Citation - Scopus: 5Adsorption Characteristics of Lead-, Barium- and Hydrogen-Rich Clinoptilolite Mineral(SAGE Publications Inc., 2003) Çakıcıoğlu Özkan, Seher Fehime; Ülkü, SemraThe carbon dioxide and water vapour adsorption properties of local clinoptilolite-rich material, both as the original and as lead-, barium- and hydrogen-rich forms, were examined. The lead- and barium-rich forms were prepared by treatment of the original clinoptilolite with Pb(NO3)2 and BaCl2 respectively, while the hydrogen-rich form was prepared by NH4Cl and heat treatment. Water and CO2 adsorption experiments were conducted in a volumetric system under static conditions, with low-pressure adsorption data being used for the characterization of the natural, Pb-rich, Ba-rich and H-rich clinoptilolite samples. Although the existence of barium-exchange was not noted, an appreciable decrease in CO2 adsorption was observed with the Pb-rich and H-rich forms due to a decrease in the electrostatic interaction between the surface and the adsorbate. Application of the Dubinin-Astakhov equation to the water adsorption data established the existence of micropores of different sizes that exhibited different adsorption mechanisms.Article Citation - WoS: 55Citation - Scopus: 60Effect of Regeneration Temperature on Adsorption Equilibria and Mass Diffusivity of Zeolite 13x-Water Pair(Elsevier Ltd., 2016) Sayılgan, Şefika Çağla; Mobedi, Moghtada; Ülkü, SemraThe adsorption equilibrium and mass diffusivity of zeolite 13X-water pair for different adsorption and regeneration temperatures were determined by a homemade volumetric system. The isotherms of the zeolite 13X-water pair were obtained by collecting pressure versus time data and applying ideal gas law. The effective diffusivity of the pair was calculated by using long term analytical solution of mass diffusivity based on Fick's law. The experimental study showed that the adsorption capacity of zeolite 13X-water pair was 23% (kg/kg), 21% (kg/kg) and 19% (kg/kg) when the adsorption temperature was 35, 45 and 60 °C respectively for the desorption temperature of 90 °C. Furthermore, the adsorption capacity increased from 22% (kg/kg) to 24% (kg/kg) when the desorption temperature was increased from 90 °C to 150 °C. It was observed that the present adsorption equilibrium results were compatible with the reported results in the literature. The mass diffusivity of the pair was found in the range of 4 × 10-9-6 × 10-8 m2/s for the long time period when the initial adsorptive pressure was 2000 Pa. The effective mass diffusivity depends on concentration and it was decreased with increasing adsorbate concentration.Article Citation - WoS: 3Citation - Scopus: 2Adsorption of No in Clinoptilolite-Rich Zeolitic Mineral by Concentration Pulse Chromatography Method(Elsevier Ltd., 2016) Narin, Güler; Ülkü, SemraThe equilibrium and kinetic parameters for NO adsorption in a clinoptilolite-rich natural zeolitic material from Turkey were determined using the concentration pulse chromatography method. Under the experimental conditions (carrier gas velocities and adsorption temperatures) the micropore diffusion resistance was found to be the mass transfer controlling step. Matching the first moment of the response peaks to the mathematical model the Henry's Law constants and heat of adsorption at zero loading were determined. The axial dispersion, external film, macropore and micropore diffusion coefficients, and activation energy for diffusion of NO in the micropores were calculated from the analysis of the second moments of the response peaks. For successive NO pulses without regeneration between the pulses, the retention times of the response peaks decreased and peak areas increased with the injection number indicating irreversible adsorption. The reversibly adsorbed NO could be desorbed by purging with an inert gas at the adsorption pressure and temperature. Temperature programmed desorption profile obtained by heating the NO saturated adsorbent to 400 °C under inert flow revealed presence of multiple irreversibly adsorbed species in NZ with different thermal stabilities. Desorption of these species was not achieved during the heating up to 400 °C which makes the natural zeolitic materıal suitable for NO storage rather than for cyclic adsorptive separation processes.Article Citation - WoS: 60Citation - Scopus: 66Preparation and Characterization of Calcium Stearate Powders and Films Prepared by Precipitation and Langmuir-Blodgett Techniques(American Chemical Society, 2010) Gönen, Mehmet; Öztürk, Serdar; Balköse, Devrim; Okur, Salih; Ülkü, SemraThe preparation of calcium stearate (CaSt2) using precipitation and Langmuir-Blodgett techniques was investigated in this study. While sodium stearate and calcium chloride were used in the precipitation process, calcium stearate nanofilms were produced from stearic acid and calcium chloride in sodium borate buffer with the Langmuir-Blodgett technique. Fourier transform infrared (FTIR) spectroscopy indicated carboxylate bands at 1577 and 1543 cm-1 in equal intensity in the powder form, but the films had a higher intensity 1577 cm-1 band than the 1543 cm-1 band. This showed the calcium ions associated with the COO- ions in the monodendate and bidendate structures in powders, and it was mainly in the bidendate structure in films. While characteristic peaks of CaSt2 at 2θ values of 6.40° and 19.58° were obtained in the X-ray diffraction (XRD) pattern of the dried powdered product, no sharp peaks were present in the 13 layer CaSt2 film. From scanning electron microscopy (SEM) micrographs, it was seen that calcium stearate powder had lamellar structure and the average particle size was 600 nm. The AFM picture of the CaSt2 film indicated the surface was not smooth with a peak to valley distance of 6 nm. © 2010 American Chemical Society.Article Citation - WoS: 15Citation - Scopus: 18Preparation and Characterization of Magnesium Stearate, Cobalt Stearate, and Copper Stearate and Their Effects on Poly(vinyl Chloride) Dehydrochlorination(John Wiley and Sons Inc., 2015) Gönen, Mehmet; Egbuchunam, Theresa Obuajulu; Balköse, Devrim; İnal, Fikret; Ülkü, SemraPreparation and characterization of pure metal soaps and investigation of their effects on poly(vinyl chloride) (PVC) dehydrochlorination were the objectives of the present study. Magnesium stearate (MgSt2), cobalt stearate (CoSt2), and copper stearate (CuSt2) were prepared by a precipitation method. An aqueous sodium stearate (NaSt) solution was mixed at 500 rpm with respective metal salt solutions at 75oC. The precipitates that formed were collected by filtration, washed with water, and ultimately dried at 105oC under reduced pressure. Lamellar crystals that melted on heating were obtained. Solid-liquid phase transitions were observed by optical microscopy at 160oC, 159oC, and 117oC for MgSt2, CoSt2, and CuSt2, respectively. However, the melting points of MgSt2, CoSt2, and CuSt2 were determined as 115oC, 159oC, and 111oC, respectively, by analysis by differential scanning calorimetry. The onset temperature of the mass loss was the lowest at 255oC for CuSt2 and the lowest activation energy for thermal decomposition was 18 kJ/mol for CuSt2. CoSt2 was effective in extending the induction time of PVC dehydrochlorination at both 140oC and 160oC. The activation energy calculated from stability time decreased from 175 kJ/mol for a blank PVC sample to 114, 105, and 107 kJ/mol for MgSt2, CoSt2, and CuSt2-containing PVC samples, respectively. All three metal soaps accelerated the dehydrochlorination of PVC. J. VINYL ADDIT. TECHNOL., 21:235-244, 2015.