Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection

Permanent URI for this collectionhttps://hdl.handle.net/11147/7148

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  • Article
    Citation - WoS: 60
    Citation - Scopus: 66
    Preparation 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, Semra
    The 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: 6
    Citation - Scopus: 8
    Dehydration, 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, Semra
    The 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: 11
    Citation - Scopus: 15
    Supercritical Carbon Dioxide Drying of Methanol-Zinc Borate Mixtures
    (American Chemical Society, 2009) Gönen, Mehmet; Balköse, Devrim; Gupta, Ram B.; Ülkü, Semra
    Supercritical 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: 22
    Citation - Scopus: 28
    The Effect of Zinc Stearate on Thermal Degradation of Paraffin Wax
    (Springer Verlag, 2008) Gönen, Mehmet; Balköse, Devrim; İnal, Fikret; Ülkü, Semra
    In this research, the effects of zinc stearate addition on paraffin wax degradation were investigated by differential scanning calorimetry (DSC) and thermogravimetry (TG). The apparent activation energies of wax decomposition in nitrogen and air atmospheres were determined as 76 and 37 kJ mol-1, respectively applying Kissinger method to TG data. The degradation rate constants of paraffin containing zinc stearate (0.1-0.5%) were found to be almost two times greater than that of paraffin only in air atmosphere. However, zinc stearate did not affect the rate constants in nitrogen significantly.
  • Article
    Citation - WoS: 34
    Citation - Scopus: 43
    Zinc Stearate Production by Precipitation and Fusion Processes
    (American Chemical Society, 2005) Gönen, Mehmet; Balköse, Devrim; İnal, Fikret; Ülkü, Semra
    In this study, the production of ZnSt2 using sodium stearate and zinc sulfate in a precipitation process, and stearic acid and zinc oxide in a fusion process, was investigated with regard to product purity. In the fusion process, an increase in mixing rate decreased the induction time occurring at the beginning of the reaction. While the melting point of the zinc stearate prepared by the precipitation process was found to be about 122°C by optical microscopy, it was slightly lower than 122°C for zinc stearate produced by the fusion process. Differential scanning calorimetry (DSC) indicated onset of melting at 120°C and 118°C for samples prepared by precipitation and fusion processes, respectively. Characteristic peaks of ZnSt2 were present in XRD patterns of the products obtained by both processes. From SEM micrographs, it was seen that zinc stearate obtained by both processes had lamellar structure.