Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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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: 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: 14Citation - Scopus: 25Kinetic and Equilibrium Studies of Adsorption of Ss-Glucuronidase by Clinoptilolite-Rich Minerals(Elsevier Ltd., 2015) Demirbüker Kavak, Dilek; Ülkü, SemraThe adsorption of the bacterial β-glucuronidase (GUS) enzyme, which is thought to be responsible for the production of reactive metabolites related to some diseases and cancer development, by clinoptilolite-rich mineral was investigated. Batch experiments were performed to analyze of the effects of the clinoptilolite amount and particle size, initial GUS concentration, shaking rate, pH and temperature on the adsorption equilibrium and kinetics. Adsorption equilibrium data were interpreted in terms of Langmuir and Freundlich isotherms; and they were well represented by the Langmuir isotherm model. The percentage of GUS removal by the clinoptilolite-rich mineral was changed in the range of 9.4-54.4% depending on its initial concentration. The kinetic data were analyzed using external film diffusion, intraparticle diffusion, pseudo-first-order and pseudo-second-order models and both external film and intraparticle diffusion appeared to be effective in GUS adsorption. Thermodynamic studies indicated that GUS adsorption is exothermic, physical and spontaneous at the temperatures investigated (288-310 K)Article Citation - WoS: 5Citation - Scopus: 8Investigation of Structural Properties of Clinoptilolite Rich Zeolites in Simulated Digestion Conditions and Their Cytotoxicity Against Caco-2 Cells in Vitro(Springer Verlag, 2013) Kavak, Dilek Demirbüker; Ülkü, SemraThe use of the clinoptilolite rich natural zeolites in biomedical applications such as in anticancer therapy, drug or drug support systems and as nutritive supplement is highly dependent on their behavior in digestive conditions. Aim of this study is to investigate structural stability of clinoptilolite rich natural zeolites in simulated digestion conditions and their interactions with digestive media and with Caco-2 (human colon adenocarcinoma) cells. X-ray Diffraction (XRD), Fourier Transform InfraRed (FTIR), Scanning Electron Microscopy (SEM) and Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) analyses of the clinoptilolite rich zeolite samples showed that zeolites preserved their structural stabilities during in vitro digestion. Slight interactions were detected in UV measurements of the digestive liquid media and FTIR spectra of the intestinal digested media powders. SEM results implied that zeolites might have a role in the aggregation of the digestive enzymes. Cytotoxicity test using colon cancer cells showed that clinoptilolite rich natural zeolites have cytotoxic effect against Caco-2 cells and cytotoxicity did not significantly change with respect to simulated digestion process.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: 10Citation - Scopus: 11Removal of Bacteria by Clinoptilolite Rich Mineral and Its Surfactant Modified Forms(Springer Verlag, 2013) Cansever Erdoğan, Beyhan; Ülkü, SemraBatch experiments were carried out to understand the potential values of clinoptilolite rich mineral and its surfactant modified forms in the removal of Gram-positive and Gram-negative bacteria. Zeta potential and Fourier Transform IR analysis were performed to explain the possible interactions between the bacteria and the zeolite samples. The results revealed that hydrogen bonding was significant mechanism in the removal of bacteria with clinoptilolite rich mineral and anionic surfactant modified clinoptilolite rich mineral whereas both attractive electrostatic forces and hydrogen bonding were dominant mechanism in the removal of bacteria with cationic surfactant modified clinoptilolite rich mineral. Cationic and anionic surfactant modified clinoptilolite rich mineral are promising materials in removal of bacteria studies.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.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.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.
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