WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7150
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Book Part Water Sorption of Polyvinyl Chloride-Luffa Cylindrica Composites(Taylor & Francis, 2014) Demir, Hasan; Balköse, DevrimNatural Luffa Cylindrica fibers were modified with 0.1M sodium hydroxide (NaOH) for removing lignin and hemicellulose. Natural and modified Luffa fibers were characterized by using IR spectroscopy. Composites were produced with PVC plastisol and natural Luffa fiber. Natural Luffa fiber is a highly hydrophilic substance. This feature increased the water sorption capacity of the composites. Flexible PVC-luffa cylindrica composites had higher liquid water sorption capacity (0.3-0.6%) compared to that of flexible PVC (0.1%). There was no volume change of composites due to liquid water sorption.Article Citation - WoS: 5Citation - Scopus: 6Use, Preparation, and Characterization of Copper-Containing Silica Gel(American Chemical Society, 2020) Ulutan, Sevgi; Tüzüm Demir, Ayşe Pınar; Balköse, DevrimThe preparation and characterization of humidity-indicating silica gel containing copper sulfate were aimed at in the present study. The equilibrium and kinetics of Cu(II) sorption were investigated by contacting 200-1600 mg dm(-3) Cu ion-containing solutions with silica hydrogel slabs having 10% silica. The diffusion coefficient of Cu(II) in silica hydrogel was determined to be on the order of 10(-10) m(2) s(-1). X-ray diffraction indicated that the gels contained mainly CuSO4 center dot 3H(2)O, CuSO4 center dot H2O, and small amounts of CuSO4 and CuSiO3 center dot 2H(2)O. The silica gel with Cu(II) can be used as a humidity indicator since its color changes from light blue to dark blue upon moisture adsorption.Article Citation - WoS: 6Citation - Scopus: 9Preparation and Characterization of Flexible Polyvinylchloride-Copper Composite Films(Smithers Rapra Technology, 2013) Kurt, Emrah; Özçelik, Cenk Yağız; Yetgin, Senem; Özmıhçı Ömürlü, Filiz; Balköse, DevrimFlexible PVC films are statically charged due to their low electrical conductivity. This creates fire threat during its handling. Conductive materials are added to films to prevent this. In the present study it was aimed to prepare PVC- copper composite films by sol gel technique and characterize the prepared films. It was aimed to increase the electrical conductivity of the films by adding copper powder. However, the copper particles settled down to bottom instead of forming a conductive network that covers the whole cross section. Thus at the film crosssection a plastic upper phase and a copper rich lower phase were present. The film did not conduct electricity due to this uneven distribution. The minimum volumetric and surface resistivities of the films were at the order of 109 ohm-cm and 1010 ohm square respectively.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: 2Citation - Scopus: 2A Study of Chemical and Physical Changes During Biaxially Oriented Polypropylene Film Production(Walter de Gruyter GmbH, 2003) Ülkü, Semra; Balköse, Devrim; Arkış, Esen; Sipahioğlu, MuzafferPolypropylene 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: 2Citation - Scopus: 2Morphology of Sodium Salt of Calf Thymus Dna on Mica, Alumina, and Silica Surfaces: Effect of Solvent and Drying Method(Taylor and Francis Ltd., 2017) Yetgin, Senem; Balköse, DevrimInvestigation of morphology of deoxyribonucleotide triphosphate (DNA) dried on different surfaces by atomic force microscopy (AFM) is important in DNA research that is focused on subjects of condensation for gene therapy, sizing, DNA mapping, and cancer examination. The solvent, the surface type, and the method of drying effect the morphology of DNA on solid surfaces. Ethanol and water were used as solvents, flat mica, silica, and alumina surfaces were used as the substrates in the present study. Different methods such as ambient air-drying, N2-forced flow regime drying, and freeze-drying have been applied to droplets of DNA solutions in water or ethanol on the substrates. Forced flow drying regime causes nonlinear DNA attachment on the surface and self-assembly. DNA vertical distance on mica surface was found to be 6 and 1.4 nm for DNA dried in ambient air from ethanol and water solutions, respectively. It was 1.6 nm for N2 flow drying of aqueous DNA solution on mica surface. It was 4.6, 4.6, and 1.99 nm for ambient, N2 flow, and freeze-dried aqueous DNA on alumina surfaces, respectively. Aqueous solution of DNA dried under N2 flow on silica surface had 0.8 nm vertical distance. The smallest standard deviation of 0.05 nm was observed for DNA dried under N2 flow on alumina surface.Article Citation - WoS: 60Citation - Scopus: 66Preparation and Characterization of Calcium Stearate Powders and Films Prepared by Precipitation and Langmuir-Blodgett Techniques(American Chemical Society, 2010) Gönen, Mehmet; Öztürk, Serdar; Balköse, Devrim; Okur, Salih; Ülkü, SemraThe preparation of calcium stearate (CaSt2) using precipitation and Langmuir-Blodgett techniques was investigated in this study. While sodium stearate and calcium chloride were used in the precipitation process, calcium stearate nanofilms were produced from stearic acid and calcium chloride in sodium borate buffer with the Langmuir-Blodgett technique. Fourier transform infrared (FTIR) spectroscopy indicated carboxylate bands at 1577 and 1543 cm-1 in equal intensity in the powder form, but the films had a higher intensity 1577 cm-1 band than the 1543 cm-1 band. This showed the calcium ions associated with the COO- ions in the monodendate and bidendate structures in powders, and it was mainly in the bidendate structure in films. While characteristic peaks of CaSt2 at 2θ values of 6.40° and 19.58° were obtained in the X-ray diffraction (XRD) pattern of the dried powdered product, no sharp peaks were present in the 13 layer CaSt2 film. From scanning electron microscopy (SEM) micrographs, it was seen that calcium stearate powder had lamellar structure and the average particle size was 600 nm. The AFM picture of the CaSt2 film indicated the surface was not smooth with a peak to valley distance of 6 nm. © 2010 American Chemical Society.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: 5Citation - Scopus: 5Methylene Blue Adsorption From Aqueous Solutions To Flexible Poly(vinyl Chloride) Silica Composites(John Wiley and Sons Inc., 2015) Yetgin, Senem; Ulutan, Sevgi; Balköse, DevrimMethylene blue (MB) adsorption studies were performed with poly(vinyl chloride)-(dioctyl phthalate)-silica composites, which were obtained by using plastisol-plastigel technology. The films were flexible, having elastic modulus of 1.0-1.5 GPa. Diminishing MB concentration in the aqueous phase was followed as the adsorption process advanced by using visible spectroscopy. Contributions of the individual components of the composites to adsorption were also investigated. Although the MB adsorption capacity was extensively high for silica, it was moderate for the composite, most likely owing to the occlusion of pores of silica by plasticizer to some extent. The improvement of MB adsorption capacity of the composites as the silica ratio increased was explicitly deduced from the optical microscopy photographs. The diffusion coefficients of MB through the composites were 5 × 10-13, 6 × 10-13, and 3 × 10-13 m2 s-1 with regression coefficients of 0.73, 0.89, and 0.88 for 0, 2, and 16% silica-containing composites, respectively. Because of the slow diffusion of MB in poly(vinyl chloride)-silica composites, using them as dynamic column adsorbent was not practical. However, these versatile plastics can be used as plastic labels, colored clothing, leather substitutes, antimicrobial medical devices, and laser printable surfaces.