Master Degree / Yüksek Lisans Tezleri

Permanent URI for this collectionhttps://hdl.handle.net/11147/3008

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  • Master Thesis
    Kinetics of Silica Polymerization at Various Conditions
    (01. Izmir Institute of Technology, 2022) Hasköylü Toker, Öykü Çağ; Demir, Mustafa Muammer; Baba, Alper
    Silica is the most abundant element on Earth because the Earth's crust is composed mainly of metal silicates. The source of this silica is mainly volcanic rocks, which come to the surface through tectonic activity and are the primary source of heat for geothermal activity. The silica concentration in a geothermal fluid is higher than the solubility limit of natural waters, so scaling of (metal) silicates is often observed in geothermal operations. This situation has become critical for geothermal power plants. Since silicates have an insulating structure, they lead to a reduction in energy efficiency during fluid transport. The formation of silica-rich deposits should be understood to minimize the negative effects of the scaling. Briefly, silicic acid molecules in the reservoir system are condensed, and the monomeric silicic acid molecules bind to each other via covalent bonds. In the course of this reaction, dimers, tetramers and short oligomers are formed, and eventually a large polymeric silica network is formed. In the presence of metals, both the kinetics of polymerization and the structure of the network are inevitably affected. In this study, the presence of kinetic parameters (different salts such as FeCl3, MgCl2, AlCl3 and NaCl), the reaction process, the rate and the activation energy of silica polymerization at different temperatures between 25 and 90 °C were investigated. The yellow silicomolybdate method was used to determine the concentration of monomeric silica. The order of the polymerization reaction was given as 3. The polymerization occurs in the initial phase, in the first 40 minutes, where the activation energy was about 29.52 ± 2.28 kJ/mol and the rate constant was of the order of 4x10-8 mol-2∙L2∙s-1. The results also confirmed that pH has a stronger effect on the kinetics of silica polymerization than temperature. The neutral solution decreases rapidly, while the acidic solution has an induction phase in the first hour of polymerization. Different temperatures did not affect the polymerization rate as much as pH. At 25°C the experiment showed the fastest polymerization, but at 90°C the low concentration changed from the beginning. During all these experiments, no scaling of amorphous silica was observed, only the polymerization of silica.
  • Master Thesis
    The Use and Characterization of Composite Alumina-Titania Membranes for Gas Separation
    (Izmir Institute of Technology, 2002) Topuz, Berna; Çiftçioğlu, Muhsin
    The preparation, characterization and pure gas permeation of sol-gel derived alumina and silica membranes were investigated in this work. The effects of various parameters on sol particle size and unsupported membranes pore structure were investigated by laser light scattering particle size and N2 adsorption-desorption analysis .-alumina membranes were prepared on ZrO2 supports by successive dipping into boehmite sols. Almost proportional decreases in sol particle size and membrane pore diameter were determined with increasing acid content during the boehmite sol preparation. Increasing the H+/Al3+ mole ratio from 0.1 to 0.25 caused the hydrodynamic particle size and BJH pore size to decrease from 65 to 30 nm and 3.6 to 2.9 nm, respectively. The pore size increased from 2.8 nm to 3 nm upon increasing the calcination temperature from 500 to 600oC. Unsupported membranes were heat treated in the 200 to 1200 oC range for the characterization of the phase structure. Boehmite was the dominant phase below 500 oC, gamma being the dominant phase up to 900 oC and pure .-Al2O3 phase was obtained upon heat treatment at 1200oC. Pinhole and crack free alumina membranes about 3 .m (double layer) in thickness were observed from SEM pictures with insignificant infiltration. The CO2 permeability through the double layer .-Al2O3 membrane calcined at 600 oC was about 2.25*10-7 mol/m2.s.Pa, and had a slight pressure dependence which may indicate Knudsen Diffusion and Laminar Flow as the effective transport mechanisms. Upon the calcination of a similar double layer alumina membrane at 500oC, the CO2 permeability decreased to 1.51*10-8 mol/m2.s.Pa and was independent of pressure. Silica membranes were prepared by a sol-gel technique. These sols were prepared by acid catalysed hydrolysis and condensation of tetraethylorthosilicate in the presence of a solvent. The effects of processing parameters like the acid type and amount utilized during sol preparation, sol aging, heat treatment conditions, dipping time on the membrane pore structure and the permeation of pure gases were investigated. The supported membranes were heat treated in the 50-400 oC range. The N2 and CO2 permeabilities of silica membranes varied in the 2.2 * 10-10 . 2.7 * 10-8 mol / m2.s.Pa and 1.2*10-9 . 6.95*10-8 mol / m2.s.Pa range for single layer membranes dipped for 10 seconds into the sol. The sols became viscous and gelled in 16 hours at 50 oC. The O2 permeability increased with aging time. The optimum dipping time during processing was determined to be 10 seconds. The permeabilities of these membranes increased significantly with the sol acid content. The thickness of the silica membranes were determined to be about 2.m and significant infiltration into the support was observed from the SEM pictures.
  • Master Thesis
    Synthesis and Characterization of Monodispere Silica Based Functional Nanoparticles for Multi-Purpose Applications
    (Izmir Institute of Technology, 2009) Altın, Burcu; Özçelik, Serdar
    The Stöber method was performed to tune the size of monodisperse silica nanoparticles in the range of 10 to 500 nm. It was observed that increasing amount of reactants favors the formation of larger particles A Stöber method in the presence of L-lysine as a catalyst instead of ammonia was developed to prepare well-ordered, highly monodisperse silica nanoparticles based on the hydrolysis and condensation of TEOS. The effect of medium temperature, amounts of L-lysine, TEOS, octane and dye on the size of particle was investigated. It was found that L-arginine increased the size of particles. The amount of TEOS was determined to be 50.0 mmol to obtain the smallest size of particle. The mole of L-lysine slightly altered the size of particles, however the surface of particles was substantially covered by L-lysine. The presence of octane does not change the size of particles. The amount of dye molecule Rhodamine B isothiocyanate (RBITC) does not alter the size of nanoparticles. We showed that temperature plays important role tuning the particle size from 5.0 nm to 80.0 nm.MTT assay indicates no cytotoxicity of the silica particles against MCF-7 (human breast cancer cell lines) and PC-3 (human prostate cancer cell lines) cancer cell lines. The particles enter to the cells within 5 minutes with a concentration of 0.1.g/mL. We propose that these particles can be used in the field of bioimaging and drug delivery.
  • Master Thesis
    Development of Liquid Armor Materials and Rheological Behavior of Shear Thickening Fluids (stfs)
    (Izmir Institute of Technology, 2011) Erdoğan, Taner; Tanoğlu, Metin
    Colloidal dispersions have been extensively used in many industrial applications such as cosmetic, paint, cement, lubricant and ceramic. Shear thickening is non- Newtonian flow behavior often observed in concentrated colloidal dispersions as an increase in viscosity with increasing shear rate or applied stress. Shear thickening fluids (STFs) exhibit fluid and solid-like properties depending on the shear rate and thus can be used in a variety of applications. In the present study, STFs have been synthesized with various weight fractions of silica nanoparticles in polyethylene glycol (PEG)/ethyl alcohol by mechanical mixing method. The steady and dynamic rheological behavior of shear thickening fluids (STFs) was investigated with rheometer. STFs thermal properties were investigated through thermogravimetric analysis. STFs have been used to improve the performance of Kevlar woven fabrics for protective applications in ballistic and stab. STFs/Kevlar fabric composites have been prepared with different impregnation techniques to evaluate the effects of the STFs. The ballistic performance and stab resistance of STFs impregnated Kevlar fabrics were investigated. Rheological measurements revealed the shear thickening effect of silica nanoparticles/PEG systems depending on the shear rate. In dynamic experiments, the strain thickening behavior was found at critical combination of strain amplitude and frequency. The viscous G modulus values were found to be greater than the elastic G modulus. The elastic G and the viscous G modulus values were found to increase when the strain amplitude is kept constant and frequency is increased. The same strain thickening behavior was also found when the frequency was kept constant and the strain amplitude was increased. The puncture resistance of STFs/Kevlar fabric composites exhibited significant improvements as compared to the neat Kevlar targets. Based on the SEM results, STFs were uniformly impregnated over the entire surface on the Kevlar fabric and Kevlar fabrics completely coated with STFs. The ballistic test results revealed STF/Kevlar fabric composites have potential to obtain liquid armor materials.
  • Master Thesis
    Use of Amine-And Mercapto-Modified Silica as Soild Phase Extraction Sorbent for Speciation of Inorganic Selenium Prior To Determination by Atomic Spectrometric Techniques
    (İzmir Institute of Technology, 2010) Dönertaş, Esen; Eroğlu, Ahmet Emin
    Silica-based sorbents containing amino-, mercapto-, and both functional groups (bifunctional) were prepared and used for the sorption of inorganic Se(IV) and Se(VI) species from waters prior to their determination by atomic spectrometric techniques, namely, inductively coupled plasma mass spectrometry (ICP-MS) and hydride generation atomic absorption spectrometry (HGAAS). The presence of the functional groups on the surface of the silica was demonstrated by using several characterization techniques such as scanning electron microscopy (SEM), solid-state NMR spectroscopy, thermo gravimetric analysis (TGA), elemental analysis and Brunauer-Emmett-Teller (BET) surface area analysis. Amine-modified silica was found to be selective towards Se(VI) at pHs 2.0 and 3.0 whereas mercapto-modified silica retains Se(IV) over a wide range from acidic regions to pH 4.0. Bifunctional silica, on the other hand, possesses the good features of the two sorbents; it can be used in the separate sorption of Se(IV) or of both Se(IV) and Se(VI) species. Acidic pHs (<1.0) are convenient for the sorption of Se(IV) alone where no sorption is observed for Se(VI). Alternatively, pH can be adjusted to 2.0 or 3.0 and Se(IV) and Se(VI) can be retained simultaneously. Desorption of selenium species from the sorbents was realized with two different eluents; 0.2% (m/v) KIO3 in 1 M HCl was used for Se(IV) and 2.0 M HCl for Se(VI). The efficiency of the proposed sorbents was demonstrated through spike recovery tests carried out with bottled drinking and tap water samples and the percentage recoveries were found to change between 82.2 ± 7.1 and 109.4 ± 3.6 for Se(IV). For Se(VI), mechanically mixed amino- and mercapto-modified (MIX) silicas in (1:1) ratio has shown the best performance with percentage recoveries of 87.1 ± 3.6 and 74.5 ± 6.6 for the spiked bottled drinking and tap water samples, respectively.