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: 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: 10Citation - Scopus: 10Morphology, Order, Light Transmittance, and Water Vapor Permeability of Aluminum-Coated Polypropylene Zeolite Composite Films(John Wiley and Sons Inc., 2011) Balköse, Devrim; Oğuz, Kaan; Özyüzer, Lütfi; Tarı, Süleyman; Arkış, Esen; Özmıhçı Ömürlü, FilizIn this study, the polypropylene-zeolite composite films having 2-6 wt % natural zeolite were coated with a thin film of aluminum (Al) by magnetron sputtering, and the contribution of the Al coating on film properties was investigated. The samples were characterized by EDX, X-ray diffraction, SEM, AFM, UV-visible spectroscopy, and water vapor permeation analyses. The surface of the films coated with a smooth Al film having 98-131 nm thickness. EDX revealed that Al percentage on the surface appeared to be as 8-10 wt % indicating contribution of polymer surface under Al film to analysis. XRD analysis showed that the grain size of Al at the surface was 22-29 nm. The surface roughness increased after Al-coating process. The transmission of coated films was very low for both UV and visible regions of the light spectrum. Permeation analysis indicated that water vapor permeation was lower for Al-coated material.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.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: 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: 44Citation - Scopus: 50Thermal Behaviour of a Zeolitic Tuff(Elsevier Ltd., 2007) Çağlar Duvarcı, Özlem; Akdeniz, Yelda; Özmıhçı Ömürlü, Filiz; Ülkü, Semra; Balköse, Devrim; Çiftçioğlu, MuhsinNatural zeolites undergo structural changes after heating which open their possible use in different fields, related to their chemical and physical properties, such as building stone, lightweight aggregate, ceramic foam, concrete bricks, tiles, porcelain stoneware and additive in puzzolonic cements. In this study, thermal behavior of zeolitic tuff quarried from Gördes-Manisa, region of Turkey was investigated. Zeolitic rocks were first reduced to 2 μm and pellets were prepared by dry-pressing. The pellets were heated for 30 min in the temperature range of 200-1200 °C. Heating the tuff up to 600 °C did not cause any structural change detectable by X-Ray powder diffraction (X-Ray), Fourier Transform Infrared Spectroscopy (FTIR) and thermal characterization methods with regard to the original sample, while further increase in the temperature caused structural breakdown of zeolitic tuff. The appearance of the broad low intensity peaks in X-Ray diffraction diagrams indicated most probably a partial transformation of crystal structure into an amorphous structure. The Scanning Electron Microscopy (SEM) micrographs showed that the crystals seen in the original rock sample were broken during grinding and pressing processes. The crystal structure disappeared above 1000 °C and the spherical pores was observed at 1200 °C. Chemical composition of the zeolitic tuff did not change significantly with respect to temperature. The highest density (2.28 g/cm3) and hardness (387 Hv) were obtained by sintering the pellets at 1000 °C for 30 min.Article Citation - WoS: 76Citation - Scopus: 84Characterization of Pure and Silver Exchanged Natural Zeolite Filled Polypropylene Composite Films(Elsevier Ltd., 2005) Pehlivan, Hilal; Balköse, Devrim; Ülkü, Semra; Tıhmınlıoğlu, FundaIn the present study, untreated and silver exchanged natural zeolite-polypropylene (PP) composites were prepared and characterized by means of different techniques (TGA, DSC, mechanical tests, density measurements, optical microscopy and colorometer). The effects of zeolite loading and silver concentration on the composite properties were investigated. The thermal characterization studies showed that the addition of the zeolite increased the crystallinity of the composites acting as a nucleating agent in PP crystallization and retarded the degradation of PP. At low silver concentrations, the zeolite behaved as a decelerating agent in PP degradation, however at higher silver concentrations, the composites degraded at a faster rate than pure PP. The experimental densities of the composites were found to be lower than the theoretical densities. When the tensile tested samples are considered, the densities were even lower indicating porous structure of the films. From the optical micrographs of the tensile tested films, it was clearly seen that the stretching along the machine direction caused hole formation around the particles. The optimum conditions obtained in this study for the PP-silver zeolite composite film production are in the range of 2-4 wt% zeolite treated with 4.36 mg Ag+/g zeolite. At higher zeolite loadings, the film becomes brittle and at higher Ag+ concentrations, the film produced was discolored.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.