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: 9Citation - Scopus: 8Measurement of Ternary Polymer/Solvent Equilibrium Data by Vapor-Phase Infrared Spectroscopy(Elsevier Ltd., 2009) Yürekli, Yılmaz; Alsoy Altınkaya, SacideVapor-liquid equilibrium (VLE) data for binary toluene/PVAC, methanol/PVAC and ternary toluene/methanol/PVAC systems have been measured at 100 °C by using vapor-phase infrared spectroscopy. Binary data have been compared with literature data measured by different experimental techniques and agreement between our measurements and others was found to be good. The ternary VLE data indicate that the solubility of methanol in PVAC is not influenced by the presence of toluene, while the solubility of toluene is lowered due to presence of methanol. To predict ternary VLE data, the Entropic free volume and Kannan free volume models and the Flory-Huggins theory were used. The predictive abilities of Flory-Huggins theory and the Kannan free volume model are similar and better than that of the Entropic free volume model.Article Citation - WoS: 12Citation - Scopus: 12The Effect of Zn Substitution of Ca in Bipbsrcacuo Superconductors Sintered at 830°c(Springer Verlag, 2009) Kocabaş, Kemal; Şakiroğlu, Serpil; Çiftçioğlu, Muhsin; Ercan, İsmail; Epik, Hakan; Bilgili, ÖzlemThe effect of partial substitution of Ca by Zn in Bi 1.7Pb 0.3Sr 2Ca 2-x Zn x Cu 3O y at x=0.00, 0.05, 0.10, 0.15 and 0.20 levels on the electrical and structural properties was investigated in this work. The characterization of the ceramics prepared by the conventional solid-state reaction method were done by resistance-temperature measurements, XRD, SEM and density analysis. Low levels of Zn substitution of Ca caused significant changes in the properties of the ceramics. The low-T c superconducting properties were enhanced and the fraction of the low-T c (2212) phase were found to increase at x=0.15 level of Zn substitution at 830°C sintering temperature. Zero resistance was observed only in sample D with x=0.15 and the T c was determined as 92 K. The SEM micrographs and the density analysis have shown that this was the densest packed ceramic.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.Article Citation - WoS: 3Citation - Scopus: 3Influence of Dispersing Agents on the Solubility of Perovskites in Water(Taylor and Francis Ltd., 2009) Şakar-Deliormanlı, Aylin; Çelik, Erdal; Polat, MehmetIn this study, solubility behavior of lead magnesium niobate (PMN) powders in water was investigated in the presence of pure polyacrylic acid and polyacrylic acid/polyethylene oxide comb polymers. Experiments were performed by measuring the solubility of PMN in terms of the concentration of Pb+2 and Mg+2 ions in supernatant as a function of pH and dispersing agent dosage. The concentrations of the metal ions in supernatant were found to be affected by the dispersant concentration, stirring time and the suspension pH. Results revealed that both dispersing agents enhance the cation dissolution from PMN surface at pH 9 due to weak (reversible) adsorption and complexation of Pb+2 and Mg+2 by carboxylate groups. On the other hand, under acidic conditions cation dissolution from PMN is inhibited and this was attributed to the strong adsorption of dispersing agents onto the powder surface and formation of a dense polymer layer.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: 68Citation - Scopus: 75Air-Water Exchange of Polychlorinated Biphenyls (pcbs) and Organochlorine Pesticides (ocps) at a Coastal Site in Izmir Bay, Turkey(Elsevier Ltd., 2008) Odabaşı, Mustafa; Çetin, Banu; Demircioğlu, Eylem; Sofuoğlu, AysunThe air-water exchange of polychlorinated biphenyl (PCB) and organochlorine pesticides (OCPs) were investigated using paired air-water samples (n = 16) collected in July and February-March, 2005 from Guzelyali Port in Izmir Bay, Turkey. Atmospheric PCBs and OCPs were mainly in gas-phase in both periods. However, their dissolved and particle-phase water concentrations were comparable. For PCBs, 3 and 4-Cl congeners were dominant while chlorpyrifos, endosulfans and HCHs were the most abundant OCPs for all samples. Especially in summer, calculated net gas-exchange PCB fluxes were mainly volatilization from the water ranging from - 0.2 (volatilization, PCB-101) to - 30.0 (volatilization, PCB-31) ng m- 2 day- 1. For OCPs, net flux ranged from - 0.03 (volatilization, cis-nonachlor) to 1568 (deposition, endosulfan I) ng m- 2 day- 1 and they have seasonal variations with generally deposition in winter and volatilization in summer. However, endosulfan I, II, endosulfan sulfate, α- and γ-HCH deposited in both periods. The calculated residence times of PCBs and OCPs in the water column indicated that the gas-exchange in the Bay is at least as or a more important mechanism than advection. Annual gaseous absorption and volatilization fluxes were calculated and were used along with the estimated dry deposition fluxes and wet deposition fluxes measured recently at a suburban site in Izmir to determine the relative contributions of different atmospheric mechanisms to the pollutant inventory of the Bay water column. Results suggested that the relative contributions of all studied mechanisms to the water column PCB and OCP inventories were significant.Article Citation - WoS: 21Citation - Scopus: 23Adsorption of Anionic Polyelectrolyte and Comb Polymers Onto Lead Magnesium Niobate(Elsevier Ltd., 2008) Şakar-Deliormanlı, Aylin; Çelik, Erdal; Polat, MehmetThis paper presents the results concerning the adsorption mechanism of polyacrylic acid (PAA) and polyacrylic acid/polyethylene oxide (PAA/PEO) comb polymer onto lead magnesium niobate (PMN) powders. In the study adsorption behavior of PAA and PAA/PEO onto PMN surface were determined in aqueous solutions and the influence of pH and ionic strength was investigated. Results showed that adsorption of PAA or PAA/PEO increased with decreasing pH of the suspensions. The increase in the ionic strength or the presence of divalent cations caused an increase in the adsorption of both polyelectrolytes. It was observed that the adsorption reaches a maximum when PAA is fully complexed in solution. On the other hand, the increase in the adsorption of PAA/PEO onto PMN in the presence of monovalent or divalent salt was attributed to the decrease in the electrostatic forces rather than complex formation with the divalent metal ions in solution. Turbidity measurements showed that there is no complex formation between the divalent metal ions and PAA/PEO comb polymers due to shielding effect of the PEO teeth.Article Citation - WoS: 53Citation - Scopus: 60Supercritical Deposition of Pt on Sno2-Coated Al2o3 Foams: Phase Behaviour and Catalytic Performance(Elsevier Ltd., 2008) Garrido, G. Incera; Patcas, F. C.; Upper, G.; Türk, M.; Yılmaz, Selahattin; Kraushaar-Czarnetzki, B.Deposition and reduction of an organometallic platinum complex from a supercritical Pt(COD)Me2/CO2 solution was carried out to produce Pt/SnO2 catalysts supported on Al2O3 foams for CO oxidation at moderate temperatures. The phase behaviour of the complex in supercritical carbon dioxide was investigated to find the optimum pressure and temperature conditions for the deposition. For the Pt(COD)Me2/CO2 mixture, the melting point decreased with increasing pressure from 378 K at 0.1 MPa to 360 K at 25.6 MPa. Additional investigations showed that the solubility of Pt(COD)Me2 in CO2 increases from 5.9 × 10-4 mol/mol at 11.2 MPa and 313 K to 3.4 × 10-3 mol/mol at 29.6 MPa and 353 K. The supercritical deposition yielded catalysts with highly dispersed platinum nanoparticles of approx. 3 nm having a narrow size distribution and thus, a superior activity towards oxidation of carbon monoxide in comparison to a catalyst prepared by the conventional aqueous impregnation of Pt.Article Citation - WoS: 15Citation - Scopus: 18Formulation and Properties' Evaluation of Pvc/(dioctyl Phthalate)/ (epoxidized Rubber Seed Oil) Plastigels(John Wiley and Sons Inc., 2008) Balköse, Devrim; Egbuchunam, Theresa Obuajulu; Okieimen, Felix EbhodagheEpoxidized rubber seed oil (4.5% oxirane content, ERSO) was prepared by treating the oil with peracetic acid generated in situ by reacting glacial acetic acid with hydrogen peroxide. The thermal behavior of the ERSO was determined by differential scanning calorimetry. The effect of the epoxidized oil on the thermal stability of poly (vinyl chloride) (PVC) plastigels, formulated to contain dioctyl phthalate (DOP) plasticizer and various amounts of the epoxidized oil, was evaluated by using discoloration indices of the polymer samples degraded at 1600C for 30 min and thermogravimetry at a constant heating rate of 10°C/min up to 600°C. The thermal behavior of the ERSO was characterized by endothermic peaks at about 150°C, which were attributed to the formation of network structures via epoxide groups, and at temperatures above 300°C, which were due to the decomposition of the material. Up to 50% of the DOP plasticizer in the PVC plastisol formulation could be substituted by ERSO without a marked deleterious effect on the consistency of the plastigel formed. In the presence of the epoxidized oil, PVC plastigel samples showed a marked reduction in discoloration and the number of conjugated double bonds, as well as high temperatures for the attainment of specific extents of degradation. These results showed that the ERSO retarded/inhibited thermal dehydrochlorination and the formation of long (n > 6) polyene sequences in PVC plastigels. The plasticizer efficiency/permanence of ERSO in PVC/DOP plastigels was evaluated from mechanical properties' measurements, leaching/migration tests, and water vapor permeability studies. The results showed that a large proportion of DOP could be substituted by ERSO in a PVC plastisol formulation without deleterious effects on the properties of the plastigels.