Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Conference Object Heavy Metal Removal Using Natural Zeolite Packed Ion Exchange Column(American Chemical Society, 2008) Balköse, Devrim; Ülkü, Semra[No abstract available]Book Part A Review: Preparation, Characterization and Applications of Magnesium Stearate, Cobalt Stearate and Copper Stearate(Nova Science Publishers, 2010) Egbuchunam, Theresa O.; Gönen, Mehmet; Balköse, Devrim; İnal, Fikret; Ülkü, SemraMetal soaps, such as zinc, calcium, copper, magnesium are insoluble or sparingly soluble in water. Because of this property, they are commercially important compounds and find applications in industry, such as driers in paints or inks, components of greases, stabilizers for plastics, in fungicides, catalysts, waterproofing agents, fuel additives, components of creams and additive in drug formulation and etc. Magnesium stearate is in widespread use as gelling, sanding and anti-sticking agents, stabilizer, lubricant, emulsifier and plasticizer for polymers, in the paint, food, rubber, paper and pharmaceutical industries. Copper stearate is used mainly for rot-proofing textiles, ropes, etc. It is also used in paints since they are soluble in oils, white spirits, etc. Quartz crystals coated with CuSt2 was used in the detection of volatile organic compounds. Cobalt stearate has applications in producing Co nests, mesoporous silica, as adhesion promoter. © 2014 by Nova Science Publishers, Inc. All rights reserved.Article Citation - WoS: 5Citation - Scopus: 7Effect of the Zeolite Filler on the Thermal Degradation Kinetics of Polypropylene(Scibulcom Ltd., 2006) Tıhmınlıoğlu, Funda; Pehlivan, Hilal; Balköse, Devrim; Ülkü, SemraIn this study, the thermal degradation behaviour of polypropylene (PP) and polypropylene-zeolite composites was investigated. Clinoptilolite, a natural zeolitic tuff, was used as the filling material into the composites. Effect of both pure clinoptilolite and silver ion exchanged form of clinoptilolite addition on the thermal degradation kinetics of polypropylene composites was studied by using differential scanning calorimetry (DSC) and thermal gravimetry analysis (TGA) techniques. Polymer degradation was evaluated by using DSC with heating rates of 5, 10, and 20 degrees C/ min from room temperature up to 500 degrees C. Silver concentration (4.36, 27.85 and 183.8 mg Ag/g zeolite) was the selected parameter under consideration. From the DSC curves, it was observed that the heat of degradation values of the composites containing 2-6% silver exchanged zeolites (321-390 kJ/kg) were larger compared to that of the pure PP free of silver and zeolite (258 kJ/kg). From the DSC results it was confirmed that PP-zeolite composites can be used at higher temperatures compared to the pure PP polymer because of its higher thermal stability. The thermal decomposition activation energies of the composites were calculated by using both the Kissenger and Ozawa models. The values predicted from these two equations were in close agreement. From the TGA curves, it was found that zeolite addition into the PP matrix speeds down the decomposition reaction, however, silver exchanged zeolite addition into the matrix accelerates the reaction. The higher the silver concentration, the lower the thermal decomposition activation energies were obtained. As a result, PP was found to be much more susceptible to thermal decomposition in the presence of silver exchanged zeolite.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: 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.Article Citation - WoS: 6Citation - Scopus: 8Dehydration, Water Vapor Adsorption and Desorption Behavior of Zn[b3o3(oh)5] · H2o and Zn[b3o4(oh)3](Taylor and Francis Ltd., 2012) Alp, Burcu; Gönen, Mehmet; Atakul Savrık, Sevdiye; Balköse, Devrim; Ülkü, SemraThe dehydration behaviors of two different hydrated zinc borate species, Zn[B3O3(OH)5] · H2O and Zn[B3O4(OH)3], which are industrially important flame retardants, were studied by thermal gravimetric(TG) analysis and in situ diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy. Dehydration onset temperatures of Zn[B3O3(OH)5] · H2O and Zn[B3O4(OH)3] were 129 and 320°C, respectively, at a 10°C/min ramp rate. A very small amount of boric acid was volatilized in addition to water vapor when both samples were heated at 250°C. A significant amount of water vapor was adsorbed by Zn[B3O3(OH)5] · H2O from air at 25°C. However, Zn[B3O4(OH)3] adsorbed a very small amount of water under the same conditions. Both zinc borates did not have a tendency to cake during storage.Article Citation - WoS: 13Citation - Scopus: 14Characterization and Dehydration Behavior of a Natural, Ammonium Hydroxide, and Thermally Treated Zeolitic Tuff(Taylor and Francis Ltd., 2011) Narin, Güler; Balköse, Devrim; Ülkü, SemraAqueous NH4OH-treated and subsequently calcined forms of local natural zeolitic tuff were characterized by different techniques including scanning electron microscopy (SEM), X-ray powder diffraction, inductively coupled plasma-atomic emission spectroscopy (ICP-AES), volumetric N2 adsorption at -196°C, thermogravimetry (TG), differential scanning calorimetry (DSC), and transmittance infrared spectroscopy. The dehydration behavior of the samples was investigated using an in situ temperature-programmed diffuse reflectance Fourier transform infrared spectroscopy (TP-DRIFTS) method under vacuum. The DRIFTS spectra recorded yielded information about the effect of the NH4OH treatment and subsequent calcination on the dehydration behavior of the natural zeolite.Changes in the infrared bands corresponding to vibrations of the O-H and N-H bonds upon in situ heating under vacuum were analyzed.