Master Degree / Yüksek Lisans Tezleri

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

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Access Right: Open AccessAuthor: search.filters.author.Kızılkaya, Ali Can

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Now showing 1 - 4 of 4
  • Master Thesis
    The Influence of Inorganic and Organic Coating Layers on the Corrosion Behaviour of Coil Coated Aluminum Substrates
    (Izmir Institute of Technology, 2020) Uç, Merve; Kızılkaya, Ali Can
    Organic coil coated aluminum substrates are one of the most widely used materials for construction industry. These coated substrates typically consist of 4 separate layers, the aluminum substrate, the inorganic conversion coating (resulting from the pretreatment application), and the organic coating layers that are called the primer and the topcoat. From industrial experience, it is not clearly and quantitatively determined how these layers contribute to the different processes that occur during corrosion, such as water uptake (diffusion of water through the coating) and the corrosion reactions that take place on the substrate. In this thesis, the formation of the inorganic conversion coating as a function of the pretreatment application parameters, immersion time, temperature and pH, and the individual effects of inorganic and organic coating layers on corrosion are investigated. The structure of the various surfaces formed after coating application and after corrosion testing by Neutral Salt Spray Test (NSST) is investigated by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDX), X-ray Fluorensence Spectrometer (XRF) and Atomic Force Microscopy (AFM) analysis, while their anticorrosive properties are determined by Electrochemical Impedance Spectroscopy (EIS). The results indicate that the formation of the pretreatment layer is enhanced continuously as function of temperature and immersion time, within the values investigated, while for pH an optimum is observed. The investigation of the corrosion resistance of substrates coated with different coating layers reveal that without organic coating layers, the substrates corrode much faster, indicating the importance of water diffusion on the corrosion reactions.
  • Master Thesis
    Effect of Sulfur on the Elementary Reactions of Fischer-Tropsch Synthesis on Cobalt Surfaces
    (Izmir Institute of Technology, 2020) Dağa, Yağmur; Kızılkaya, Ali Can
    Industrial observations indicate that sulfur acts a poison for Fischer-Tropsch Synthesis (FTS) and surface science studies show that sulfur blocks the adsorption sites for reactants on cobalt surfaces. However, various experimental studies have indicated conflicting results about the effect of sulfur on cobalt FTS catalyst activity and selectivity. This study aims to clarify the effect of sulfur on cobalt FTS catalysts by molecular modelling of the elementary reactions of FTS on surfaces that are present on sulfur covered cobalt surfaces that are present in fcc-Co nanoparticles, using Density Functional Theory (DFT). For 0.25 ML sulfur coverage, it is found that on bare, C and O covered surfaces, S is the main dissociation product, while HS can be present on low coverages. Atomic sulfur decreases the adsorption energies of all species investigated, while the decrease is more pronounced for CO compared to H2. The effect of S on the elementary FTS reactions direct and H-assisted CO dissociation, carbon hydrogenation, carbon coupling and oxygen removal are also investigated. The results indicate that S inhibits mainly the oxygen removal reaction, in terms of both H2O and CO2. CO dissociation is not inhibited but rather slowed down, due to increasing activation barriers. It is also found that carbon hydrogenation barriers are significantly decreased, while carbon coupling barriers are unaffected. These results indicate that the intrinsic effect of sulfur poisoning would be to increase methane selectivity, while decreasing the selectivity to long chain hydrocarbons.
  • Master Thesis
    Effect of Aging Electrolyte and Organic Coating Type on the Corrosion Mechanism of Tinplate
    (Izmir Institute of Technology, 2019) Yıldırım, Koray; Kızılkaya, Ali Can; Çağlar, Başar
    Market share of the can coating industry was 2 billion dollars in 2018 globally. A large portion of this market is focused on protecting valuable goods such as foods and cosmetics. Recent bans on the Bisphenol A(BPA) created a BPA-free coating demand due to the high portion of BPA based coatings in the industry such as epoxy. A conventional epoxy based (EP) can coating was compared with a new design of BPAfree polyester coating(PE). Atomic Force Microscopy(AFM), Scanning Electron Microscopy(SEM), Electron Dispersive Spectroscopy(EDX), Electrochemical Impedance Spectroscopy(EIS), Direct Current(DC) Polarization were used to investigate degradation. Industrial and model tinplate samples are compared with surface investigation methods. AFM results indicate the surface composition difference. To investigate bare tinplate corrosion, a mixture of acidic electrolyte was prepared and compared with other conventional aging electrolytes, containing mono acids. The electrolyte prepared from mixed acids was found to have the highest detinning abilities. Therefore, coated samples were aged with this mixed acid solution electrolyte. EIS results indicated that the type of electrolyte alters the corrosion mechanism, indicated by the observance of different time constants at different time scales. During immersion tests, EP based coatings showed better corrosion resistance as shown by higher impedance at low frequency, higher coating resistance and lower capacitance values. However, after sterilization, polyester coated samples showed better corrosion protective abilities (indicated by lower amount of corrosion products and higher impedance values) compared to the epoxy sample even though AFM measurements indicated that it had larger pore sizes after aging compared to epoxy sample. These results are attributed to the larger electrochemical area and higher diffusion properties of EP coatings, obtained after modelling of EIS data.
  • Master Thesis
    Effects of Manganese Promotion on Reactants and Intermediates of Fischer Tropsch Synthesis on a Model Cobalt Surface-A Density Functional Theory Investigation
    (Izmir Institute of Technology, 2019) Gençoğlu, Merve; Kızılkaya, Ali Can; Sevinçli, Haldun
    The effects of manganese promotion on the adsorbates and specific elementary reactions of Fischer-Tropsch Synthesis (FTS) was investigated using periodic Density-Functional Theory (DFT) calculations on a close packed cobalt surface, Co(111). In particular the effects of MnO promotion on the adsorbates of CO, HCO, CH, CH2, C2H2, OH, H2O, C, O and on the reactions of direct CO dissociation, H-assisted CO dissociation and carbon hydrogenation were studied for MnO coverages of 0.25 ML and 0.11 ML. Mn was modeled in the chemical form of MnO. MnO was modeled as a singular monomer on the Co(111) surface, based on the findings from experimental studies. The results indicate that MnO promotion increases the adsorption energies of all adsorbates, except H and C2H2. In particular, CO and H2O adsorption energies increase significantly, which indicate that the selectivity increases to long chain hydrocarbons is mainly due to an increased surface coverage of CO with respect to H. The results also indicate that the relative effect of MnO on adsorption energies are strongly dependent on MnO coverage. MnO promotion is found to decrease the activation barriers for HCO and CH formation, while increasing the activation barriers for direct CO dissociation and HCO dissociation. The results point out that MnO does not promote the direct dissociation of CO and the activity increase due to Mn promotion is most probably due to a H or OH assisted CO dissociation pathway or another rate limiting step.