Chemical Engineering / Kimya Mühendisliği

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

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  • Conference Object
    Antioxidant, Antimicrobial and Cytotoxic Activities of Some Turkish Plant Extracts
    (John Wiley and Sons Inc., 2006) Altıok, Evren; Asbagh, L. Abbasi; Bulut, Çisem; Ülkü, Semra; Bayraktar, Oğuz
    Plant extracts have been known to possess notable biological activity, including antioxidant, antimicrobial and cytotoxic properties. There is a growing interest in the use of natural products in the human food industries as consumer resistance to synthetic additives increases. These products can be used to improve human health. In vitro antioxidant, antimicrobial and cytotoxic activities of ethanol extracts of some plants from Urla region in Turkey were investigated. Plant materials were collected from Pistacia lentiscus, Vitex agnus-castus, Cistus creticus and Nerium oleander in October, November and December.
  • 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: 8
    Citation - Scopus: 8
    Phase Equilibrium and Diffusion of Solvents in Polybutadiene: a Capillary-Column Inverse Gas Chromatography Study
    (John Wiley and Sons Inc., 2002) Cai, W. D.; Ramesh, N.; Tıhmınlıoğlu, Funda; Danner, Ronald P.; Duda, John Larry; De Haan, A.
    The capillary-column inverse gas chromatography method was used to measure the diffusion and partition coefficients of ethylbenzene, styrene, and acrylonitrile in polybutadiene (PBD) at infinite dilution of the solvents. Experiments were performed over a temperature range of 50-125°C. At temperatures well above the glass-transition temperature of PBD, the diffusivities were correlated using an Arrhenius expression. The Arrhenius parameters in turn were intercorrelated and shown to be a function of the occupied volume, thus providing a method for predicting the diffusion of other solvents in the same polymer. Further, the activation energy was predicted using the Duda-Vrentas free-volume approach. The activation energy thus obtained was compared with the activation energy of the Arrhenius approach. The weight-fraction activity coefficient data were compared to the predictions of the group contribution, lattice-fluid equation-of-state, and the UNIquac Functional-group Activity Coefficient (UNIFAC) free-volume models.
  • Article
    Citation - WoS: 15
    Citation - Scopus: 18
    Formulation 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 Ebhodaghe
    Epoxidized 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.
  • Article
    Citation - WoS: 17
    Citation - Scopus: 18
    Crystallization of Poly(vinyl Alcohol) During Solvent Removal: Infrared Characterization and Mathematical Modeling
    (John Wiley and Sons Inc., 2007) Wong, Sim-Siong; Alsoy Altınkaya, Sacide; Mallapragada, Surya K.
    Crystallization of semicrystalline polymer films during drying has a significant effect on the rate of solvent removal. Understanding and controlling the crystallization kinetics is important in controlling residual solvent levels and drying kinetics. The degree of crystallinity of the poly(vinyl alcohol) films during multicomponent drying was investigated using Fourier transform infrared spectroscopy (FTIR). The 1141 cm-1 band is sensitive to the degree of crystallinity of the polymer and the growth of intensity of this band was monitored as drying progressed. The results from the FTIR studies were comparable to the results obtained from differential scanning calorimetry. Studies were conducted to test the effect of initial solvent composition (water-methanol mixture), drying temperature, and polymer molecular weight on the rate of crystallization and the final crystallinity of the films. An increase in initial methanol composition increased the crystallization rate but did not affect the final degree of crystallinity. An increase in drying temperature and decrease in polymer molecular weight increased the rate of crystallization as well as the final degree of crystallinity. Based on the experimental data, rate constants for crystallization kinetics were extracted from our previously developed model based on free volume theory. The experimental data and the simulation results showed good agreement. The ability of the free volume theory to illustrate the crystallization behavior validated the model and improved its capability.
  • 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.
  • Article
    Citation - WoS: 13
    Citation - Scopus: 15
    Determination of Thermodynamic and Transport Properties of Solvents and Non Solvents in Poly(l-Lactide
    (John Wiley and Sons Inc., 2006) Eser, Hülya; Tıhmınlıoğlu, Funda
    Thermodynamic properties, partition coefficient, and diffusion coefficients of the various solvents (acetone, dichloromethane, trichloromethane, ethyl acetate, ethyl alcohol, tetrahydrofuran, and water) in poly(lactide-co- glycolide) (PLGA) at infinite dilution of the solvent have been determined by inverse gas chromatography (IGC). In IGC method, which is based on the characteristic equilibrium partitioning of a solute between a mobile phase and a stationary phase, a small pulse of solvent is introduced into the column and by the aid of retention volume of the solvent, several polymer solvent interaction properties, namely retention volume (Vg), infinitely dilute weight fraction activity coefficient (Ω1∞), Flory-Huggins interaction parameter (χ), and solubility parameters of the polymer (δ2∞) can be determined. The thermodynamic results indi cated that trichloromethane and dichloromethane were the most suitable solvents among all the solvents studied for PLGA. The partition (K) and diffusion coefficients (Dp) of various solvents at infinite dilution of the solvent were calculated by using the model developed by Pawlisch et al. (Macromolecules 1987, 20, 1564). The optimum K and D p values that best fit the data were found and the model predicted experimental data very well. So IGC method is a powerful tool for the determination of thermodynamic and diffusion properties of solvent in polymer at infinite dilution of the solvent.
  • Article
    Citation - WoS: 64
    Citation - Scopus: 70
    Mechanical and Morphological Properties of Recycled High-Density Polyethylene, Filled With Calcium Carbonate and Fly Ash
    (John Wiley and Sons Inc., 2006) Atikler, Ulaş; Başalp, Dildare; Tıhmınlıoğlu, Funda
    In this study, mechanical and morphological properties of composites made up of recycled high-density polyethylene (HDPE) filled with calcium carbonate and fly ash (FA) were studied. Interfacial interactions were modified to improve the filler compatibility and mechanical properties of the composites by surface treatment of the FA filler with 3-amino propyl triethoxy silane. The composites were prepared by using a Thermo Haake Rheomixer. Effect of filler loading and treatment of FA with silane coupling agent on mechanical and morphological properties were investigated and it was found that silane treatment indicated significant improvements on the mechanical properties of the HDPE-FA composites. The improvement with silane treatment of FA was also confirmed by applying the Pukanszky model. Scanning electron microscopy on the fracture surface of composites had given direct evidence of better interfacial adhesion via silane treatment.
  • Article
    Citation - WoS: 22
    Citation - Scopus: 21
    A Novel Silk Fibroin-Supported Iron Catalyst for Hydroxylation of Phenol
    (John Wiley and Sons Inc., 2006) Pekşen, Bahar Başak; Üzelakçil, Caner; Güneş, Alev; Malay, Özge; Bayraktar, Oğuz
    The aim of this study was to explore the potential use of silk fibroin (SF) as a catalyst support material for phenol hydroxylation reactions. Iron-substituted silk fibroin fibers were prepared using formic acid at room temperature and characterized using inductively coupled plasma atomic-emission spectrometry, scanning electron microscopy, Fourier transform infrared spectroscopy (FTIR) and optical microscopy. Measurement of an FTIR spectrum showed that the secondary structure was β-structure before and after iron substitution. To evaluate the catalytic properties of prepared catalyst, phenol hydroxylation reaction was carried out using aqueous hydrogen peroxide as an oxidant. An excellent transformation of phenol into dihydroxybenzenes (catechol and hydroquinone) was achieved. Phenol conversions of 3.3%, 61.2%, and 80.3% were obtained at room temperature, 40°C and 60°C respectively. It was found that no further phenol conversion proceeded because catalysts became separated from the reaction system during the reaction. No significant leaching of the iron was detected. Catalyst could be reused several times without a significant change in activity. Parent silk fibroin fibers without iron were inactive.