Thesis (M.S.) in Chemical Engineering--University of Maine, 2002. / Includes vita. Includes bibliographical references (leaves 69-72).

Metal oxides are important materials that are being developed for use in research and health-related applications. In particular, TiO2 and ZnO nanomaterials for applications in antibacterial coatings, pollutant purification, and photovoltaic devices have been extensively studied. The photocatalytic performances are highly dependent on morphology and crystal structure. However, there are few studies are comparing pollutant purification and antibacterial behavior of different TiO2 nanostructures and less studies of antibacterial activity related to fundamental properties of ZnO. In this study, the details of proposed mechanism and principle of antibacterial mechanisms of metal oxide nanostructures has been examined. Different TiO2 nanostructures (nanotubes, nanorods) have been successfully synthesized and their photocatalytic properties have been studied. In addition, studies of basic properties of commercial ZnO nanoparticles related to antibacterial activity have been performed. / published_or_final_version / Physics / Master / Master of Philosophy

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The structure of the oxide/aqueous electrolyte interface has been studied. The surface porosity of several oxides to ions is evaluated and the contribution of such porosity to the double layer properties determined by surface charge measurements. The oxides studied are B.D.H. precipitated silica, before and after heat treatment, rutile, goethite, hematite and amorphous ferric oxide. The surface porosity was evaluated using nitrogen adsorption for physical porosity, tritium exchange for surface hydration and dissolution for surface crystallinity. It is found that the surfaces of metal oxides may be divided into two categories; those that are porous to ions and those that are non-porous. Of those studied only the precipitated silica and the amorphous ferric oxide are porous. The porosity is probably due to an easily permeated layer of hydrolysed oxidic material. It does lead to exceptionally high surface charges. However the non-porous oxides also exhibit high surface charges so that while surface porosity may, in some cases, contribute to oxide double layer properties, it cannot be a general explanation of the high differential capacities observed. A site-binding model for non-porous oxide/aqueous electrolyte interfaces is introduced, in which it is proposed that the adsorbed counter ions form interfacial ion pairs with discrete charged surface groups. This model is used to calculate theoretical surface charge densities and potentials at the Outer Helmholtz Plane. The calculated values are consistent with experimental data for oxides provided a high value of the inner zone capacity is accepted. An explanation is provided for the difference between silica and most other oxides in terms of the dissociation constants of the surface groups.

Thesis (Ph.D)--Chemical Engineering, Georgia Institute of Technology, 2009. / Committee Chair: Teja, Amyn S.; Committee Member: Abdel-Khalik, Said I.; Committee Member: Meredith, Carson; Committee Member: Nair, Sankar; Committee Member: Skandan, Ganesh. Part of the SMARTech Electronic Thesis and Dissertation Collection.

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The purpose of this study was: (1) to find the effect of temperature on the wet oxidation of chalcopyrite, pyrite, and copper sulfide over the biological and nonbiological range; (2) to determine the influence of ferrous and ferric iron and free oxygen(air) on the oxidation. The sulfide minerals studied were oxidized over a range of temperatures between 25° to 75° C. The optimum biological oxidation occurred near 35° C. The nonbiological oxidation was very slow at low temperatures but increased with increasing temperature. The effect of solutions used in leaching the various sulfides over the temperature range differred. A synthetic nutrient solution, containing only a source of phosphate and nitrogen, was more effective on the biological oxidation of pyrite than on copper sulfide at the optimum temperature. Tailings water, obtained from Bingham Canyon, Utah, was more effective on chalcopyrite over a long period of time than the synthetic nutrient. Ten times more chalcopyrite was oxidized at 70° C. than at 55° C. in a dilute solution of sulfuric acid. A dilute solution of ferrous sulfate had very little effect on the oxidation of the sulfides. Oxygen and ferric iron in oxidized tailings water were shown to affect the oxidation of chalcopyrite at 65° C. The ferric iron was reduced. In an atmosphere of nitrogen, ferrous iron in fresh tailings water was inactive on the oxidation of chalcopyrite. Oxygen is the primary oxidizing agent in the biological and nonbiological oxidation of sulfide minerals in the leaching process.

A Dissertation submitted to the Faculty of Science, School of Chemistry, University of Witwatersrand in fulfillment of the requirements for the degree of Master of Science. Johannesburg 2014 / The resin-gel method of synthesis successfully produced compounds of mixed metal oxides of copper titanium oxide powders of the form CuxTiyOZ with different compositions. These include Cu3TiO5, Cu3TiO4, Ti3Cu3O, Cu2Ti4O, Cu2Ti2O5 and Cu2TiO3. Heat-treatment of the powders at 300°C, 500°C, 700°C and 900°C for 1 hour was performed to determine the full composition/temperature phase diagram. The target particle size was in the 10- nanometer range, and for most of the samples, this size was achieved. Powder xray diffraction and transmission electron microscopy were the main techniques used to study the crystallization of these materials and their transformation to other polymorphic phases under different temperatures. Phase-match, particle size analysis and TEM imaging determined the properties and characteristics of the respective crystallographic phases of these materials. TEM analysis showed that some powders agglomerated while others exhibited both regular and irregular morphologies and polydisperse particle size distribution. Only a single unique phase was identified, but its structure could not be determined.