Ti thin films were deposited by a radio frequency ion-beam sputtering system. Deposition resulted from sputtering a Ti target (99.995%) with an Ar ion beam. Epitaxial TiO thin films with different orientations, which came from oxidizing Ti thin films, were prepared on single-crystal NaCl substrate. The formation of epitaxial TiO2 thin films (anatase or rutile phase) by oxidation of epitaxial TiO thin films was investigated. The composition, microstructure, and orientation relationships between interfaces were analyzed by TEM and Fourier transformation in the present report. Epitaxial TiO thin films with different orientations were prepared on single-crystal NaCl substrate in the present study. The formation of epitaxial TiO2 thin films (anatase or rutile) by oxidation of epitaxial TiO thin films, which were first grown on different NaCl surfaces, was investigated. The composition, microstructure, and orientation relationships between interfaces were analyzed by TEM and Fourier transformation in this report. The TiO to anatase phase transformation has been studied by transmission electron microscopy in this Article. It is shown that prior formation of TiO from Ti film can induce the formation of anatase by thermal oxidation in air, otherwise only rutile is formed. Ti film deposited on the NaCl (001) surface is induced to form epitaxial TiO film by thermal oxidation in air. Further thermal oxidation in air partially transformed TiO into anatase (A) with a parallel orientation relationship of {200}A // {200}TiO. Detailed analysis of the lattice fringes image of the specimen reveals the presence of very high density of misfit dislocations. The TiO to anatase transformation is reversible as further annealing in a vacuum can turn the anatase back into TiO and eliminates the misfit dislocations. The transformation is analyzed in terms of the crystal structure, orientation relationship, and the dislocation distribution, which show that the TiO to anatase transformation is due to the close similarity between their structures. (Chapter 1) The anatase TiO2 (001) surface was shown to have superior photoreactivity. Epitaxial anatase (001) films used to be grown on single-crystal SrTiO3 and LaAlO3 substrates. It is shown in this report that these films can be grown also on the NaCl substrate, which is much cheaper and easily prepared. Epitaxial TiO (001) films were first grown on the NaCl (001) substrate. By testing the TiO-to-anatase transformation over temperature and time ranges, an epitaxial anatase (001) film was prepared by simple thermal oxidation in air. The formation of a single-variant anatase (001) film instead of a multiple-variant film is discussed in this report. (Chapter 2) An epitaxial rutile (100) thin film has been grown on NaCl substrate instead of other more expensive substrates. An epitaxial TiO (111) thin film with minor Ti phase was first deposited on the NaCl (111) surface by thermal evaporation. It was then transformed into the epitaxial rutile (100) thin film by subsequent thermal oxidation in air. TEM was used to analyze the phases and the orientation relationship. Our previous result showed that an epitaxial anatase (001) film was formed on the NaCl (001) surface in a similar process. The substrate-dependent formation of different TiO2 phase is also discussed in terms of the mismatch of the interfaces. (Chapter 3)

This experiment use NaCl (001) single crystal as substrate, and the target is zinc oxide, to generate a-plane (112 ¡Â0) zinc oxide nanothim. The nanofilm is used as a buffer layer generating by Ion Beam Sputtering, and then increasing the thickness by Plasma sputtering. Part of specimens to proceed atmospheric heat treatment with different temperature and time, and part of specimens to change the ratio of the gas when the thin film is growth, then use of Transmission electron microscopy (TEM) and Photoluminescence (PL) as the analysis of film properties. The results of experiment, show that (112 ¡Â0) plane have more stringent conditions when generate of thin film, and easy to become the ring of electron diffraction with no-epitaxy .But finally we get a data what can generate a well a-plane ZnO thin film, the substrate temperature of 400 ¢X C, the sputtering time of 1 hour, Ar/O2 = 1.5. From the results of Photoluminescence, we find that there are zinc vacancies in ZnO thin film, probably there are too many oxygen atoms. While the heat treatment in nitrogen, zinc vacancies are reduced rapidly. Indicating that oxygen atoms within the film are reduced by nitrogen atoms or replace the position of the oxygen atoms.

It is particularly intriguing in the role of the solid-state dopants, which are not only responsible for the semiconductivity, but also the dielectric properties of BaTiO3 ceramics, e.g. CaO, MgO, Y2O3, CoO and MnO2 for EIA-X7R characteristics. We have chosen to investigate three important processing parameters, oxygen partial pressure (pO2) for sintering, and two alkali-earth-metal oxides, i.e. CaO and MgO for solid-state additives in order to study how microstructure and dielectric properties are determined by them. They are used in MLCC industry for the effect in attaining X7R characteristics and protecting against or improving for dc degradation. Apart from establishing the temperature-dependent dielectric properties, i.e. temperature-coefficient of capacitance (TCC), for both qualitative and quantitative analysis, crystalline phases in sintered ceramics of tetragonal mixed with cubic, orthorhombic and rhombohedral phases are studied using XRD and Raman spectroscopy. For microscopic studies, SEM and TEM techniques, e.g. CBED and LACBED, combined with EDS are used to study phases both in core-shell. We will examine and confirm the fidelity of whether core-shell grains are induced by chemical inhomogeneity, and more importantly, if the diffuse phase transition is caused by such microstructure with direct observations, as previous studies in perovskite-related ceramics, and crystalline phase determination for these grains. It is also an objective that we investigate why and how, by what mechanism, the chemically similar alkali-earth metal oxides should impart completely different (and indeed opposite) effect in protecting against dc degradation. Keywords: MLCC, dc degradation, DPT, Raman spectroscopy, electron microscopy.

Apatite is one of the accessory minerals in the UHP metamorphosed eclogites at Northern Dulan belt, North Qaidam. It appears in three kinds of occurrences: (1) included in garnet which often shows cracks along the apatite grains, (2) coexisting with omphacite, rutile and/or clinozoisite in matrix and often surrounded by garnet, and (3) coexisting with retrograded minerals. The three eclogite samples examined in the present study are enriched in garnet. Two of them contain up to 80 vol.% garnet and the other is a porphyry of medium-grained garnet. They commonly show cracks and features of retrograde metamorphism, such as fissure-filling of secondary minerals including calcite or greenschist facies minerals. There are two size-ranges of well-oriented sulfide minerals included in apatite. One is nanometer-sized sulfide needles (50 ¡Ñ 20 ~ 870 ¡Ñ 120 nm) and particles (55 ~ 370 nm). The other is micrometer-sized sulfide needles (~20 ¡Ñ 0.5 £gm) and rods (~2.5 ¡Ñ 0.5£gm). Fluid inclusions and the micrometer-sized sulfide minerals commonly occur in the apatite grains that are near the cracks. Both nanometer- and micrometer-sized sulfide minerals are elongated with their long axes being normal or parallel to the c axis of the apatite. We used SEM-EDS and TEM-EDS to analyze and found that the sulfide minerals are troilite, pyrrhotite, Cu-bearing pyrrhotite and chalcopyrite. There are two sets of preferred crystallographic orientations for the dominated troilite and host apatite. The rod troilite is elongated along its a axis and <001>troilite // <001>apatite, <48-3>troilite ∡ <13-3>apatite = ~ 0.6º, (2-10)troilite // (3-10)apatite, <100>troilite ∡ <100>apatite = ~ 10º. The needle troilite is also elongated along its a axis and <001>troilite ¡æ <001>apatite, <-110>troilite ∡ <-12-2>apatite = ~ 1.3º, (11-2)troilite // (0-1-1)apatite. The preferred crystallographic orientation relationships, in terms of the c axis of troilite being parallel or normal to the c axis of host apatite, are similar to those for oriented quartz precipitates and omphacite hosts in the previous studies. According to the observations that only few sulfide minerals included in other minerals, the occurrences of apatites, and the microtextures of sulfide minerals, we suggest that the origin of sulfide minerals may relate to metasomatism during plate subduction. Metal ions such as iron, copper, cobalt and nickel were carried by chlorine- and sulfur-enriched fluids, which might be trapped as primary fluid inclusions in the apatite. The sulfide minerals then formed at the sites of fluid inclusions with the aid of fluids and available ions.

Fatigue crack growth in ±-Zirconium phosphate/epoxy nanocomposites was investigated. A new fatigue testing technique was implemented for miniature samples. Two different methods “strength of materials and Rayleigh-Ritz - were used in determining the bending stress. The fatigue stress and fatigue life of different nanocomposite specimens were plotted in a traditional stress-life (S-N) curve. It was inferred from the S-N plot that the values obtained from both the methods compare well. The experimental results showed that fatigue life of filled epoxy nanocomposite is more than that of the unfilled epoxy composite. A model for bending stresses, ultimate strength and the number of cycles to failure was obtained to predict a component service life without conducting elaborate tests. Scanning electron examination of the fractured surfaces revealed that the crack takes a tortuous path during its propagation course, indicating crack blunting and crack deflection roles of ZrP and CSR nanofillers, which consequently improve the fracture resistance. In case of the M-ZrP-epoxy systems, delamination of ZrP platelets from surrounding epoxy matrix was proposed as the reason behind crack growth. The improved fracture resistance of these nanocomposites was attributed to the delamination of ZrP platelets and deflection of crack direction. The superior behavior of CSR-ZrP-epoxy composites was attributed to the cavitation process and void coalescence due to CSR particles delamination.

Increase in consumption of fresh produce over the past decade has resulted in a rise in incidents of foodborne outbreaks due to pathogens. Chemical sanitizers have been extensively used in the industry for decontamination of fresh produce. However, they are ineffective in certain commodities and under certain processing conditions, necessitating the evaluation of alternative technologies. Electron beam irradiated sliced cantaloupe were tested for 21 days of storage for total aerobic bacterial counts, texture, color and sensory parameters as a function of irradiation doses 0, 0.7 and 1.4 kGy and the wash treatments, water and 200 mg/L chlorine applied to the melons before cutting. Melons washed only with water prior to cutting had total aerobic bacterial counts of 4.0, 2.0 and 0.8 log cfu/g on day 0 at irradiation doses of 0, 0.7 and 1.4 kGy respectively. On day 0, melons washed with chlorine prior to cutting had total aerobic bacterial counts of 2.7, and 0.7 log cfu/g at irradiation doses of 0 and 0.7 kGy and below detection limit at 1.4 kGy. Texture measured as compression force was lower only for cantaloupe irradiated at 1.4 kGy. Irradiation did not affect objective color and descriptive attribute flavor and texture sensory attributes of cantaloupe. Irradiation reduced Salmonella Poona by 1.1 log cfu/g at 0.7 kGy and 3.6 log cfu/g at 1.5 kGy. The D-value of S. Poona on irradiated sliced cantaloupe was found to be 0.211 kGy. Among the spoilage organisms, lactic acid bacteria and mold were reduced effectively by irradiation but there was no significant effect on reduction of yeasts. Our results show that electron beam irradiation in combination with chemical sanitizers is effective in decontamination of fresh-cut produce. Electron microscopy images provided valuable information on attachment sites of S. Poona on cantaloupe rind. The ineffectiveness of chemical sanitizers due to possible inaccessibility to pathogens in these attachment sites provides the basis for application of irradiation in decontamination of fresh produce.

Thesis (Ph. D.)--University of Kentucky, 2003. / Title from document title page (viewed June 30, 2004). Document formatted into pages; contains xv, 150 p. : ill. Includes abstract and vita. Includes bibliographical references (p. 140-148).

Thesis (M. Phil.)--Hong Kong University of Science and Technology, 2003. / Includes bibliographical references (leaves 58-59). Also available in electronic version. Access restricted to campus users.

Nanoparticles possess unique physical, chemical, optical and electronic properties stemming from their nanoscale dimensions and are currently used in catalysis, microelectronics, drug delivery, as well as other applications. However, due to their large surface area-to-volume ratio, nanoparticles have a strong tendency to coalesce and sinter during processing or usage over short time scales and at low temperatures, which lead to significant changes in behavior and performance. In this work, in-situ transmission electron microscopy (TEM) heating has been used to investigate the effects of particle size, temperature and carbon capping layers on sintering in face-centered cubic (FCC) metallic nanoparticles. For the first time, we make direct and real-time measurements of nanoparticle size, neck growth, dihedral angle and grain boundary motion during sintering, which are then used to calculate fundamental material transport parameters such as surface diffusivity and grain boundary mobility. We observe that carbon surface coatings typically present on most commercial nanoparticles can significantly inhibit sintering in nanoparticles. Also, a new mechanism for coalescence in nanoparticles is shown where small clusters on the support can initiate neck growth by forming a bridge between the nanoparticles consisting of individual atoms or small clusters of atoms. In-situ TEM experiments provide critical and valuable real-time dynamic information for direct investigation of the link between the evolution of sintering and controlling mechanisms, which conventional experiments such as post-mortem TEM observations are not capable of conveying. / text

Semiconductor nanowires are one-dimensional nanoscale systems that exhibit many unique properties. Their nanoscale size can lead to defect densities and impurity populations different than bulk materials, resulting in altered diffusion behavior and mechanical properties. Synthetic methods now support the large-scale production of semiconductor nanowires, enabling a new class of materials and devices that use macroscopic quantities of nanowires. These advances have created an opportunity to fabricate bulk structures which exhibit the unique physical properties of semiconductor nanowires, bridging the properties of a nanoscale system with macroscopic materials. High aspect ratio germanium nanowires were synthesized in supercritical organic solvents using colloidal gold nanocrystal seeds. The nanowires were chemically passivated inside the reactor system using in situ thermal hydrogermylation and thiolation. The chemical stability of the passivated nanowires was studied by exposure to highly corrosive and oxidative environments. Chemical surface functionalization of germanium nanowires was investigated by covalently tethering carboxylic acid groups to the surface, as a general platform for the further functionalization of nanowire surfaces with molecules such as polyethylene glycol. Surface functionalization with dopant-containing molecules was also explored as a potential route for doping nanowires. In addition, static charging was exploited in the development of an electrostatic deposition method for semiconductor nanowires. In situ transmission electron microscopy experiments were conducted on gold-seeded germanium nanowires encapsulated within a volume-restricting carbon shell. A depressed eutectic melting temperature was observed, along with strong capillary effects, and the solid-state diffusion of gold into the crystalline stem of the germanium nanowire, occurring at rates orders of magnitude slower than in the bulk. Copper, nickel, and gold diffusion in silicon nanowires were also investigated. The rate of gold diffusion was found to be a strong function of the amount of gold available to the system. Finally, germanium nanowires were found to exhibit exceptional mechanical properties, with bending strengths approaching that of an ideal, defect-free, perfect crystal, and strength-to-weight ratios greater than either Kevlar or carbon fiber. Macroscopic quantities of nanowires were used to fabricate large sheets of free-standing semiconductor nanowire fabric, and the physical, morphological, and optical properties of the material were investigated. / text