WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7150
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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]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: 11Citation - Scopus: 15Supercritical Carbon Dioxide Drying of Methanol-Zinc Borate Mixtures(American Chemical Society, 2009) Gönen, Mehmet; Balköse, Devrim; Gupta, Ram B.; Ülkü, SemraSupercritical carbon dioxide (CO 2) drying of zinc borate species was investigated to evaluate possible chemical alterations in the product during the drying. Methanol-wetted zinc borates produced either from borax decahydrate and zinc nitrate hexahydrate (2ZnO · 3B 2O 3 ·7H 2O) or from zinc oxide and boric acid (2ZnO · 3B 2O 3 ·3H 2O) were dried by both conventional and supercritical carbon dioxide drying methods. Zinc borate samples dried by both techniques were characterized using analytical titration, X-ray powder diffraction (XRD), thermo gravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, elemental analysis, and scanning electron microscopy (SEM). It was found that while zinc borate obtained from zinc oxide and boric acid did not have any chemical interaction with CO 2, carbonates were formed on the surface of zinc borate obtained from borax decahydrate and zinc nitrate hexahydrate. The main factor for the carbonate formation during supercritical CO 2 drying is anticipated as the structural differences of zinc borate species. CO 2 is a nonpolar solvent, and it does not usually react with polar substances unless water is present in the medium. While 2ZnO · 3B 2O 3 ·3H 2O had three bound OH groups, 2ZnO · 3B 2O 3 ·7H 2O had five bound OH groups and one mole of water of crystallization. It is proposed that the water of crystallization reacts with CO 2 forming carbonic acid. Then, carbonic acid, which is stronger than boric acid, substitutes borate ions from their zinc salts.Conference Object Citation - WoS: 18Citation - Scopus: 19Development of Synergistic Heat Stabilizers for Pvc From Zinc Borate-Zinc Phosphate(Taylor and Francis Ltd., 2009) Erdoğdu, Cem Aykut; Atakul, Sevdiye; Balköse, Devrim; Ülkü, SemraThe importance of flame-retardant and smoke-suppressed poly(vinyl chloride) (PVC) compositions is increasing gradually in the polymer industry since PVC releases smoke and toxic gases (hydrogen chloride, HCl) during heating at temperatures above 140°C with the result of dehydrochlorination reaction. In this study, the synergistic effects of zinc borate (ZB)-zinc phosphate (ZP) on the thermal stability of PVC were investigated using thermal techniques. The induction and stability time values of PVC plastigels were obtained at 140°C and 160°C. The results revealed that PVC plastigels having only ZP and ZB retarded dehydrochlorination of PVC compared with the unstabilized sample. However, the plastigels with both ZB and ZP had a superior synergistic effect on char formation of PVC. Since the induction periods of the samples having both ZB and ZP were higher than those of the unstabilized samples having only ZB or only ZP, the synergistic effect was observed.Conference Object Citation - WoS: 2Citation - Scopus: 2Studies in the Utilization of Biobased Additives as Thermal Stabilizer for Plasticized Pvc(Trans Tech Publications, 2009) Okieimen, Felix Ebhodaghe; Egbuchunam, Theresa Obuajulu; Balköse, DevrimDivalent metal (barium, cadmium, calcium and zinc) soaps of rubber seed oil and their binary mixtures (BaJCd and CaJZn) and epoxidized rubber seed oil (4.5% epoxide content) and its admixtures with the single divalent metal soaps were evaluated as thermal stabilizer for dioctylphthalate plasticized PVC using changes in discolouration indices (yellowness index and UV absorption at 360nm) and initial rates of dehydrochlorination measured at 140 and 160°C. The results obtained showed that the divalent metal soaps were relatively effective in stabilizing the dioctylphthalate plasticized PVC against thermal degradation and that the binary soap mixtures enhanced the heat stabilizing effectiveness: marked reduction in the values of the discolouration indices; longer dehydrochiorination induction period and smaller values of rate constant of initial rate of dehydrochlorination. It was found that epoxidized rubber seed oil was less effective in comparison with the divalent metal soaps in stabilizing plasticized PVC against thermal degradation. These results show that the bio-based additives are compatible with dioctylphthalate plasticized PVC, stable to heat within the range of temperature used in the processing of plasticized PVC, inhibitlretard dehydrochlorination and reduce the extent of degradation.Article Citation - WoS: 51Citation - Scopus: 58Effect of Additives on Flexible Pvc Foam Formation(Elsevier Ltd., 2008) Demir, Hasan; Sipahioğlu, Muzaffer; Balköse, Devrim; Ülkü, SemraIn this study, effects of Ca/Zn stearate and organotin heat stabilizers and zeolite, CaCO3, cellulose and luffa flours fillers, and their concentrations (2.5, 5, 10 and 20% by weight) on production of flexible PVC foams by chemical blowing agent, azodicarbonamide were investigated. Foam morphology, foam density, compressive mechanical properties and water uptake capacities of samples were determined. Morphology of the sample without any filler showed that employment of Ca stearate and Zn stearate heat stabilizers instead of organotin stabilizers increases foam formation and decreases pore sizes and regularity in pore size distribution. Foams having organotin stabilizer were more resistant to heat than the ones with Ca/Zn stearate for long heating periods. Foams, including organotin-based heat stabilizers, have compact structure. It was observed that, samples containing zeolite, CaCO3, cellulose or luffa flour had lower pore volume but higher Young's modulus and stress values compared to unfilled samples.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.