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Corrosion behavior of ion plated filmsPaul, George Doll 12 1900 (has links)
No description available.
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162 |
Effects of thermal aging on the mechanical behavior of K3B matrix material and its relationship to composite behaviorSacks, Serena 08 1900 (has links)
No description available.
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163 |
A study of tin oxide-based gas sensors with nanostructureZhang, Gong 08 1900 (has links)
No description available.
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164 |
Nondestructive evaluation of damage in SiC/Al metal matrix composite using x-ray tomographic microscopyBreunig, Thomas M. 05 1900 (has links)
No description available.
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The structure of the oxide/aqueous electrolyte interfaceYates, David Edwin January 1975 (has links)
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.
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Non Newtonian viscosity of bulk metallic glass forming liquids and the ordering and shear rate induced crystallization of undercooled Zr₄₁ ₂Ti₁₃ ₈Cu₁₂ ₅Ni₁₀ ₀Be₂₂ ₅ metallic glass forming melt /Wadhwa, Prashant. January 1900 (has links)
Thesis (Ph. D.)--Oregon State University, 2008. / Printout. Includes bibliographical references. Also available on the World Wide Web.
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167 |
Syntheses and studies of metal(II) complexes of the potentially heptadentate schiff base ligands derived from 2,2', 2"-triaminotriethylamine and 2-pyridinecarboxaldehyde or 6-methyl-2-pyridinecarboxaldehyde.Wilson, Lonnie James, January 1971 (has links)
Thesis (Ph. D.)--University of Washington. / Bibliography: l. 119-122.
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168 |
Heat transfer during consolidation of metal matrix composites by the hip processBaci, Francesca M. January 1997 (has links)
Thesis (M.S.)--Ohio University, November, 1997. / Title from PDF t.p.
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169 |
Preparation and characterization of metal soap nanofilms/Öztürk, Serdar. Balköse, Devrim January 2005 (has links) (PDF)
Thesis (Master)--İzmir Institute of Technology, İzmir, 2005. / Keywords: Electrical conductivity, langmuir blodgett technique, metal soaps, nanofilms, moisture adsorption. Includes bibliographical references (leaves. 127-132).
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170 |
Chemically modified electrodes with inorganic films of noble metal complexes and metal oxides : preparation, characterization and applications /Han, Qi. January 2002 (has links)
Thesis (M. Phil.)--Hong Kong University of Science and Technology, 2002. / Includes bibliographical references. Also available in electronic version. Access restricted to campus users.
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