Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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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: 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: 11Comparison of Uniform and Non-Uniform Pressure Approaches Used To Analyze an Adsorption Process in a Closed Type Adsorbent Bed(Springer Verlag, 2013) Gediz İliş, Gamze; Mobedi, Moghtada; Ülkü, SemraHeat and mass transfer in an annular adsorbent bed filled with silica gel particles is numerically analyzed by uniform and non-uniform pressure approaches. The study is performed for silica gel-water pair, particle radius from 0.025 to 1 mm and two bed radii of 10 and 40 mm. For uniform pressure approach, the energy equation for the bed and the mass transfer equation for the particle are solved. For non-uniform pressure approach, the continuity and Darcy equations due to the motion of water vapor in the bed are added, and four coupled partial differential equations are solved. The changes of the adsorbate concentration, pressure, and temperature in the bed throughout the adsorption process for both approaches are obtained and compared. The obtained results showed that the particle size plays an important role on the validity of uniform pressure approach. Due to the interparticle mass transfer resistance, there is a considerable difference between the results of the uniform pressure and non-uniform pressure approaches for the beds with small size of particles such as 0.025 mm.Article Citation - WoS: 3Citation - Scopus: 3Heat and Mass Transfer in the Adsorbent Bed of an Adsorption Heat Pump(Taylor and Francis Ltd., 2011) Demir, Hasan; Mobedi, Moghtada; Ülkü, SemraThe heat and mass transfer equations governing an adsorbent bed in an adsorption heat p mp and the mass balance equation for the adsorbent particles in the adsorbent bed were solved numerically to simulate the cycle of a basic adsorption heat pump, which includes isobaric adsorption, isosteric heating, isobaric desorption, and isosteric cooling processes. The finite difference method was used to solve the set of governing equations, which are highly nonlinear and coupled. The pressures of the evaporator and condenser were 2 and 20 kPa, respectively, and the regeneration temperature of the bed was 403 K. Changes in the temperature, adsorptive pressure, and adsorbate concentration in the adsorbent bed at different steps of the cycle were determined. The basic simulated cycle is presented in a Clausius-Clapeyron diagram, which illustrates the changes in average pressure and temperature of the adsorbent bed throughout the cycle. The results of the simulation indicated that the most time-consuming processes in the adsorption heat pump cycle were isobaric adsorption and isobaric desorption. The high thermal resistance of the bed slows down heat transfer, prolonging adsorption and desorption processes.Article Citation - WoS: 12Citation - Scopus: 13Statistical Thermal Stability of Pvc(John Wiley and Sons Inc., 2010) Atakul Savrık, Sevdiye; Cansever Erdoğan, Beyhan; Balköse, Devrim; Ülkü, SemraExperimental design was used to optimize the processing parameters for the decomposition of poly (vinyl chloride). Factorial design and face centered composite design (FCC) were applied to determine the optimum conditions. A total of 10 g PVC powder was mixed with different amounts of zinc stearate (ZnSt 2) and natural zeolite and tested for thermal stability. Factorial fitted model was explained by first order pattern due to the significant main effect regression constants, and FCC model was described by second order model owing to higher order polynomial coefficients. FCC design was superior to factorial design as FCC considers not only its pure quadratic effects contribution but also its higher overall desirability for thermal stability of PVC. For factorial design the optimum conditions were determined as 163.06 mg for ZnSt2, 399.99 mg for zeolite, and 140°C for temperature with desirability of 0.933. However, 400 mg for ZnSt2, 333.24 mg for zeolite, and 140°C for temperature with desirability of 0.956 were obtained as the optimum conditions by FCC design. © 2010 Wiley Periodicals, Inc.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.Article Citation - WoS: 18Citation - Scopus: 19Effect of Zeolite Filler on the Thermal Degradation Kinetics of Polypropylene(John Wiley and Sons Inc., 2006) Pehlivan, Hilal; Balköse, Devrim; Ülkü, Semra; Tıhmınlıoğlu, FundaIn this study, the thermal degradation behavior of polypropylene (PP) and PP-zeolite composites was investigated, Clinoptilolite, a natural zeolitic tuff, was used as the filler material in composites. The effects of both pure clinoptilolite and silver-ion-exchanged clinoptilolite on the thermal degradation kinetics of the PP composites was studied with differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Polymer degradation was evaluated with DSC at heating rates of 5, 10, and 20°C/ min from room temperature to 500°C. The silver concentration (4.36, 27.85, and 183.8 mg of Ag/g of zeolite) was the selected parameter under consideration. From the DSC curves, we observed that the heat of degradation values of the composites containing 2-6% silver-exchanged zeolite (321-390 kj/kg) were larger than that of the pure PP (258 kj/kg). From the DSC results, we confirmed that the PPzeolite composites can be used at higher temperatures than the pure PP polymer because of its higher thermal stability, The thermal decomposition activation energies of the composites were calculated with both the Kissinger and Ozawa models. The values predicted from these two equations were in close agreement. From the TGA curves, we found that zeolite addition into the PP matrix slowed the decomposition reaction; however, silver-exchanged zeolite addition into the matrix accelerated the reaction. The higher the silver concentration was, the lower were the thermal decomposition activation energies we obtained. As a result, PP was much more susceptible to thermal decomposition in the presence of silver-exchanged zeolite.Article Citation - WoS: 8Citation - Scopus: 10Moisture Sorption and Thermal Characteristics of Polyaramide Blend Fabrics(John Wiley and Sons Inc., 2006) Genç, Gözde; Alp, Burcu; Balköse, Devrim; Ülkü, Semra; Cireli, AysunFour types of fabrics woven from various polyaramid fibers of Nomex and Kevlar blends were characterized by morphology, XRD, elemental analysis, thermal analysis, and moisture adsorption isotherms. The blends consisted of Polybenzimidazole/ Kevlar blend (40% FBI and 60% Kevlar®), Nomex Delta A (blend of 60% Kevlar and 40% Nomex®), Nomex Delta T (blend of 75% Nomex, 23% Kevlar, and 2% P140 antistatic fiber), and Nomex III (fabric with a 95/5 blend of Nomex and Kevlar) containing 1% steel fiber. TGA and DTG curves have been compared to evaluate thermal behavior of the FBI, Kevlar, and Nomex blends and the resuls were correlated with the moisture sorption data. The data were also compared with fiber morphologies provided by SEM and crystallinities derived from XRD diffrac tograms. Moisture adsorption isotherms were correlated with a number of empirical models, including Nernst, Freundlich, Handersen, Iglesias-Chirife, and with the models having a theoretical background such as Langmuir, BET, GAB, and Hüttig. The linear regression models were statistically analyzed to obtain the best fitting model that explains the sorption profiles of the samples and theoretical monolayer moisture capacities of Nomex and Kevlar blends were calculated by using Hüttig isotherms.Article Citation - WoS: 4Citation - Scopus: 4A Chromatographic Study of Carbon Monoxide Adsorption on a Clinoptilolite-Containing Natural Zeolitic Material(Taylor and Francis Ltd., 2004) Narin, Güler; Yılmaz, Selahattin; Ülkü, SemraIn this study, the equilibrium and kinetic parameters for CO adsorption on clinoptilolite-rich natural zeolitic material were determined by the concentration pulse chromatography technique. Experiments were carried out at different column temperatures (60-120°C) and interstitial carrier gas velocities (3.1-16.3 cm/s) using a clinoptilolite-rich natural zeolitic material packed column. The equilibrium and kinetic parameters were determined by matching the moments of the experimentally obtained response curves to the parameters in the mathematical model. The Henry's Law constants were found to decrease from 700 to 49 with increasing temperature. The heat of adsorption at low coverage was found to be 50.73 kJ/molK. The contributions from external film, macropore, and micropore diffusion resistances to mass transfer were determined, and the micropore diffusion resistance was found to be the major contributor. The micropore diffusivity as a function of crystal radius (Dc/rc 2) was determined and found to change between 5.72 × 10-4 and 1.34 × 10-2 s-1 in the temperature range studied.Article Citation - WoS: 30Citation - Scopus: 31Water and Water Vapor Sorption Studies in Polypropylene-Zeolite Composites(Wiley, 2003) Pehlivan, Hilal; Özmıhçı, Filiz; Tıhmınlıoğlu, Funda; Balköse, Devrim; Ülkü, SemraWater and water vapor sorption to porous polypropylene-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 films samples having different zeolite loadings (6-40 wt %). Because PP is a hydrophobic polymer, it does not sorp any water, but the composites having 10, 20, 30, and 40% zeolites have sorbed 0.63, 1.00, 1.72 and 3.74% water, respectively. The zeolite itself at the same conditions sorbed 24.5% water. As the filler loading in the composites increased, equilibrium uptake values increased also. On the other hand, water vapor sorption and kinetics has been studied using a Cahn 2000 gravimetric sorption system. Within in the range of 0.35-0.95% water vapor was adsorbed by the composites containing 10-40 wt % zeolites. Experimental effective water vapor diffusivities of the composite films was about one order of magnitude higher (10-fold) 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.