Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

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  • Article
    Citation - WoS: 8
    Citation - Scopus: 9
    Polymeric Thermal Analysis of C+h and C+h+ar Ion Implanted Uhmwpe Samples
    (Elsevier Ltd., 2007) Kaya, N.; Öztarhan, Ahmet M.; Urkaç, Emel Sokullu; Ila, D.; Budak, S.; Oks, E.; Tıhmınlıoğlu, Funda; Muntele, C.
    Chemical surface characterization of C + H hybrid ion implanted UHMWPE samples were carried out using DSC (differential scanning calorimeter) and TGA (thermal gravimetric analysis) techniques. Samples were implanted with a fluence of 10(17) ion/cm(2) and an extraction voltage of 30 kV. The study of TGA and DSC curves showed that: (1) Polymeric decomposition temperature increased, (2) T-m, Delta C-p and Delta H-m values changed while Delta C-p and Delta H-m increased. T-g value could not be measured, because of some experimental limitations. However, the increase in Delta H-m values showed that T-g values increased, (3) the branch density which indicated the increase in number of cross-link (M-c) decreased in ion implanted samples and (4) increase in Delta H-m values indicated increase in crystallinity of implanted surface of UHMWPE samples.
  • Article
    Citation - WoS: 2
    Catalytic Activity of Heteropolytungstic Acid Encapsulated Into Mesoporous Material Structure
    (Walter de Gruyter GmbH, 2007) Gündüz, Gönül; Dimitrova, Rayna P.; Yılmaz, Selahattin
    The paper presents a spectroscopic and catalytic study of encapsulated Keggin type heteropoly acid (12-tungstophosphoric acid, HPW) in the mesopores of MCM-41 molecular sieves. Nitrogen physisorption, FTIR, SEM, XRD and catalytic methods have been used to characterize and compare the properties of the samples. Methanol conversion, alpha-pinene isomerization and ethyl acetate oxidation have been applied as model reactions for the evaluation of acid site activity. The combined physicochemical and catalytic investigations clearly show that the introduction of 12-tungstophosphoric acid into MCM-41 causes significant changes in the properties of the sample.
  • Article
    Citation - WoS: 2
    Citation - Scopus: 10
    Water 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, Semra
    Water 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: 2
    Citation - Scopus: 2
    A Study of Chemical and Physical Changes During Biaxially Oriented Polypropylene Film Production
    (Walter de Gruyter GmbH, 2003) Ülkü, Semra; Balköse, Devrim; Arkış, Esen; Sipahioğlu, Muzaffer
    Polypropylene 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: 12
    Citation - Scopus: 12
    The 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, Özlem
    The 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.
  • Conference Object
    Citation - WoS: 18
    Citation - Scopus: 19
    Development of Synergistic Heat Stabilizers for Pvc From Zinc Borate-Zinc Phosphate
    (Taylor and Francis Ltd., 2009) Erdoğdu, Cem Aykut; Atakul, Sevdiye; Balköse, Devrim; Ülkü, Semra
    The 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: 9
    Citation - Scopus: 10
    Hydrogenation of Citral Over Ni and Ni-Sn Catalysts
    (TUBITAK, 2008) Aykaç, Hilal; Yılmaz, Selahattin
    Liquid phase citral hydrogenation over zeolite-supported monometallic Ni and bimetallic Ni-Sn catalysts was studied. The zeolite support materials were Na-Y, Na-mordenite, and clinoptilolite. Ni and Sn contents of the monometallic and bimetallic catalysts were 8.1-9.2 wt% and 0.46 wt%, respectively. The type of the zeolite support affected the activity and selectivity of the catalysts differently. The main product of the citral hydrogenation reaction was citronellal, for both monometallic (84.5% yield) and bimetallic (44.5% yield) catalysts. The addition of promoter increased the selectivity to unsaturated alcohols (geraniol+nerol), i.e. it changed from 0.9% to 6.3% over mordenite and from 0.9% to 2.1% over Na-Y-supported catalysts. Furthermore, activity of the Ni catalysts decreased while the quantity of acetal remained almost constant. Intimate contact between active metal, promoter, and support, and a catalyst with a high concentration of weak acid sites gave high selectivity to geraniol+nerol.
  • Article
    Citation - WoS: 3
    Citation - Scopus: 3
    Hydrogenation of Citral Over Pt and Pt-Sn Catalysts
    (TUBITAK, 2008) Aykaç, Hilal; Yılmaz, Selahattin
    Hydrogenation of citral on monometallic (Pt) and bimetallic (Pt-Sn) catalysts was investigated. It was found that the catalyst activities and product distributions were different over Na-Y and Clino supports. Among monometallic catalysts, Pt/Na-Y was more selective to citronellol (3.9%) and unsaturated alcohols, geraniol and nerol, (14.1%). Sn addition increased the catalyst activities. However, its effect on product distribution differed. Yield of geraniol+nerol changed from 5.1% to 19.7% over Clino. However, selectivity to unsaturated alcohols over Na-Y decreased when it was prepared as a bimetallic catalyst support. Unsaturated alcohol formation was favored when there was a metal support interaction over monometallic catalysts, and metal-promoter interaction over bimetallic catalyst.
  • Article
    Citation - WoS: 18
    Citation - Scopus: 19
    Effect of Zeolite Filler on the Thermal Degradation Kinetics of Polypropylene
    (John Wiley and Sons Inc., 2006) Pehlivan, Hilal; Balköse, Devrim; Ülkü, Semra; Tıhmınlıoğlu, Funda
    In 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: 8
    Citation - Scopus: 10
    Moisture Sorption and Thermal Characteristics of Polyaramide Blend Fabrics
    (John Wiley and Sons Inc., 2006) Genç, Gözde; Alp, Burcu; Balköse, Devrim; Ülkü, Semra; Cireli, Aysun
    Four 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.