Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 3Citation - Scopus: 4Photocatalytic and Optical Properties of Zinc Oxide Structures Prepared at Different Urea Concentrations(Serban Solacolu Foundation, 2020) Uysal, Berk; Şen, Selin; Top, AybenIn this study, ZnO samples were synthesized using zinc acetate and urea with a method containing sonication, sol-gel transition and calcination steps. Urea to zinc acetate mole ratio values were changed as 0, 0.5, 1, and 2 and corresponding calcined samples were denoted as UZ-0, UZ-0.5, UZ-1, and UZ-2, respectively. Scanning electron microscopy (SEM) images indicated globular and rod-like structures. Aspect ratios of the nanorods increased as urea to zinc acetate ratio increased from 0 to 1 whereas nanoparticles with sizes of 70 +/- 20 nm were observed for UZ-2 sample. Brunauer, Emmett and Teller (BET) surface area values of the samples varied between 9 and 25 m(2)/g and increased as initial urea amount increased. Band gap energies of the samples ranged between 3.24 and 3.29 eV. Four major peaks at about 400, 420, 480 and 530 nm with different intensities were observed in the photoluminescence (PL) spectra of the samples. All the samples removed rhodamine B by both adsorption and photodegradation. The highest visible light induced photodegradation rate was exhibited by UZ-2 sample having the highest surface area and it is attributed to superior charge separation properties of this sample under visible light.Article Citation - WoS: 4Citation - Scopus: 4Optical and Photocatalytic Properties of Zno and Zns Structures Formed as Controlled Calcination Products of L-Cysteine Assisted Aqueous Precipitation(Elsevier, 2020) Şen, Selin; Top, AybenZnO and ZnS structures were obtained by the calcination of the aqueous precipitation products of Zn(NO3)2, NaOH and L-cysteine (Cys). Initial Cys:Zn molar ratios were changed as 0.1:1, 0.5:1, 1:1 and 1.5:1. All the precursors were transformed into ZnO upon calcination at 700 °C. ZnS structures were obtained by calcining the precursors prepared at the Cys:Zn ratios of 1 and 1.5 at 350 °C. In addition to changing chemical composition of the precipitation products, calcination temperature and initial Cys:Zn ratio also affected morphology, surface area, photoluminescence and photocatalytic properties of the final products. Free exciton energy values of the ZnO samples were observed to be between 3.29 eV and 3.35 eV. PL spectra of the ZnO samples indicated blue and green emission centers. Zinc interstitials (Zni), revealed by the blue emissions in the PL spectra were also confirmed by Auger Zn L3M4.5M4.5 spectra. The samples calcined at 350 °C removed rhodamine B mainly by adsorption. All the samples calcined at 700 °C successfully degraded the dye under UV light. Among the samples calcined at 700 °C, ZnO sample prepared at Cys:Zn = 0.5, which has the highest surface area and unique photoluminescence spectrum exhibited the fastest photodegradation rate. © 2020 Elsevier LtdArticle Citation - Scopus: 1Optical and Surface Properties of Zinc Oxide Nanoparticles Dried by Conventional and Supercritical Ethanol Drying Techniques(Research India Publications, 2014) Egbuchunam, Theresa Obuajulu; Yetgin, Senem; Özmıhçı Ömürlü, Filiz; Balköse, DevrimZinc oxide (ZnO) nanoparticles were synthesized by conventional (ZnO-A) and supercritical ethanol drying (ZnO-B). Nitrogen adsorption/desorption analyses were performed to determine the surface areas of the powders. The specific surface area was 28.30m2/g and 10.61 m2/g for ZnO-A and ZnO-B respectively. The powders adsorbed very small amount of CO2with the conventionally dried powder adsorbing more CO2. Supercritical ethanol dried ZnO had ethanol on its surface which was eliminated by vacuum application at room temperature. Both powders had OH groups which were eliminated on heating up to 500°C under vacuum. However, OH groups were present in lower amounts in supercritical ethanol dried ZnO. The powders were characterized by UV-VIS optical absorption and room temperature photoluminescence spectroscopic analyses. The UV-VIS absorption spectrum showed an absorption band at 375nm due to ZnO nanoparticles. The photoluminescence spectrum of ZnO excited at 380nm exhibited three emission peaks: one at 424nm and 490nm corresponding to band gap excitonic emission and another located at 520nm due to the presence of singly ionized oxygen vacancies.Article Citation - WoS: 6Citation - Scopus: 7Preparation and Characterization of Flexible Poly(vinyl Chloride) Foam Films(John Wiley and Sons Inc., 2012) Şahin, Erdem; Yaşar Mahlıçlı, Filiz; Yetgin, Senem; Balköse, DevrimIn this study, the effect of activator ZnO and heating time at 190°C on foaming, gelation, and dehydrochlorination of poly(vinyl chloride) (PVC) plastisol was investigated. For this purpose, a PVC plastisol was prepared by mixing PVC, dioctyl phthalate (DOP), azodicarbonamide (ADC), ZnO, and the heat stabilizers calcium stearate (CaSt 2) and zinc stearate(ZnSt 2). PVC plastisol films were heated for 3, 6, 12, and 24 min periods at 190°C to see the effect of heating time on the gelation and foaming processes of the PVC foam. The time of 12 min was determined to be optimum for the completion of gelation and foaming processes without thermal degradation of PVC. No foaming was observed under the same conditions for the samples without ZnO. ZnO had a significant catalytic effect on ADC decomposition, accelerating the foaming of the films. Average porosity measurement showed a consistent increase in porosity with heating time up to 76% and the average density decreased from 1.17 to 0.29 g/cm 3 on foaming. Tensile tests showed that the tensile strength and tensile strain both increased considerably up to 0.98 MPa and 207%, respectively, with heating time and the elastic modulus was seen to gradually decrease from 4.7 to 0.7 MPa with heating time. Films without ZnO had higher tensile strength since there were no pores. PVC thermomat tests showed that ZnO lowered the stability time of plastigel film with azodicarbonamide.Article Citation - WoS: 19Citation - Scopus: 20Isothermal Crystallization Kinetics and Mechanical Properties of Polycaprolactone Composites With Zinc Oxide, Oleic Acid, and Glycerol Monooleate(John Wiley and Sons Inc., 2013) Alp, Burcu; Cesur, SerapThe isothermal crystallization and mechanical behavior of polycaprolactone (PCL) with zinc oxide (ZnO) with oleic acid and glycerol monooleate (GMO) were studied. Theoretical melting points calculated by the Flory-Huggins and Thompson-Gibbs models were thoroughly compared with differential scanning calorimetry experimental observations. The isothermal crystallization kinetic parameters by Avrami analysis showed that crystallization was controlled by nucleation, crystal growth was spherical, and the nucleation type changed between thermal and athermal nucleation. X-ray diffraction showed that when the additives were used together both the crystal thickness and the degree of crystallinity increased. A multiple-response regression analysis was made with the ZnO, oleic acid, and GMO concentrations as variables and the crystallinity as output. Interaction parameters by the Pukanzky model were calculated from the tensile strength at the yield point and indicated that the addition of oleic acid or GMO improved the interface between the ZnO particles and PCL.Article Citation - WoS: 17Citation - Scopus: 21Effects of Particle Size and Electrical Resistivity of Filler on Mechanical, Electrical, and Thermal Properties of Linear Low Density Polyethylene-Zinc Oxide Composites(John Wiley and Sons Inc., 2013) Özmıhçı Ömürlü, Filiz; Balköse, DevrimThe effects of particle size and electrical resistivity of zinc oxide (ZnO) on mechanical properties, electrical and thermal conductivities of composites made with linear low density polyethylene (LLDPE) were investigated. Micron sized (mZnO), submicron sized (sZnO), and nano sized (nZnO) powders having resistivities of 1.5 × 106, 1.5 × 109, and 1.7 × 108 were used to prepare composites with 5-20 vol % filler. The tensile strength was lowered and the modulus of elasticity of the composites was increased with ZnO addition. Rather than the particle size of the ZnO, its initial resistivity and aspect ratio affected the resistivity of composites. The resistivity of the LLDPE was lowered from 2.3 × 1016 Ω cm down to 1.4 × 1010 Ω cm with mZnO addition. Thermal conductivity of the composites was increased with ZnO addition 2.5-3 times of the polymer matrix. The composites can be used for electrostatically dissipating and heat sink applications due to their decreased electrical resistivity and increased thermal conductivity.Article Citation - WoS: 10Citation - Scopus: 13Effect of Supercritical Ethanol Drying on the Properties of Zinc Oxide Nanoparticles(Taylor and Francis Ltd., 2012) Egbuchunam, Theresa; Balköse, DevrimThe synthesis, characterization, and application as polymers and anti-wear additives of nanosized zinc oxide particles obtained by conventional and supercritical ethanol drying are reported in this study. The nanaoparticles of ZnO produced by the two different drying techniques were characterized using Fourier Transform Infrared (FT-IR) spectrophotometry, Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD) and Thermogravimetric analysis (TGA) to elucidate the shape, size, composition, and stability of the nanoparticles. ZnO nanoparticles were then applied to poly (vinyl chloride) (PVC) powder and light mineral oil to assess their effectiveness and suitability as additives in diverse areas. XRD analysis revealed ZnO crystalline structure with average particle size of 24.7 nm for zinc oxide nanoparticles prepared by supercritical ethanol drying while SEM showed well-isolated and monodisperse particles with average size of 61.08 nm. © 2012 Copyright Taylor and Francis Group, LLC.Article Citation - WoS: 20Citation - Scopus: 19The Catalytic Reforming of Bio-Ethanol Over Sio2 Supported Zno Catalysts: The Role of Zno Loading and the Steam Reforming of Acetaldehyde(Elsevier Ltd., 2008) Şeker, ErolIn this study, the activity and the product distributions of sol-gel made SiO2 supported ZnO catalysts in the steam reforming of ethanol and acetaldehyde is presented as a function of ZnO loading and temperature. We show that although highly dispersed ZnO in SiO2 (upto 50% ZnO loading) can be prepared using a single step sol-gel method, a precise control of crystallite size could not be achieved. From CO2 TPD measurements, we found that the basic site densities of ZnO/SiO2 catalysts stays < 0.05 μ mol / m2 and do not increase linearly with ZnO loading. The highest basic site density among the catalysts occurs on pure ZnO. All ZnO/SiO2 catalysts are active at 350 °C whereas pure ZnO catalyst is active at 450 °C. Iso-conversion activity tests show that ethanol steam reforming activities of the catalysts seem to be dependent on the ZnO crystallite size rather than the basic site density of the catalysts when the surface coverage of the basic site density is < 0.32 % but acetone is not formed only on catalysts with ZnO crystallite size < 5 nm regardless of their basic site densities. Interestingly, we found that ethanol was mostly dehydrogenated to acetaldehyde and hydrogen although H2O/C2H5OH molar ratio in the feed was 12. CO was not also produced in the steam reforming of ethanol over all the catalysts. Acetone and propene are produced from acetaldehyde as observed in the steam reforming of acetaldehyde. The steam reforming of acetaldehyde as compared to its decomposition was found to be more favorable over the catalysts with small ZnO crystals, such as 30% and 50% ZnO catalysts.