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  • 1
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 84 (2001), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The high-temperature creep behavior of two fine-grained (∼3 μm) anorthite-rich glass-ceramics was characterized at ambient pressure and under a confining pressure of ∼300 MPa. Experiments were done at differential stresses of 15–200 MPa and temperatures of 1200°–1320°C. Of the two materials, one had a tabular (lathlike) grain structure with finely dispersed second phase of mullite, mostly in the form of ∼3–5 μm grains comparable to that of the primary anorthite phase, whereas the other had an equiaxed grain morphology with fine (∼400 nm) mullite precipitates concentrated at the anorthite grain boundaries. The results of creep experiments at ambient pressure showed that the material with the tabular grain structure had strain rates at least an order of magnitude faster than the equiaxed material. Creep in the tabular-grained material at ambient pressure was accompanied by a significant extent of intergranular cavitation: pore-volume analysis before and after creep in this material suggested that 〉75% of the bulk strain was due to growth of these voids. The equiaxed material, in contrast, showed a smooth transition from Newtonian (n= 1) creep at low stresses to non-Newtonian behavior at high stresses (n 〉 2). Under the high confining pressure, the microstructures of both materials underwent significant changes. Grain-boundary mullite precipitates in the undeformed, equiaxed-grain material were replaced by fine (∼100 nm), intragranular precipitates of silliminate and corundum because of a pressure-induced chemical reaction. This was accompanied by a significant reduction in grain size in both materials. The substantial microstructural changes at high confining pressure resulted in substantially lower viscosities for both materials. The absence of mullite precipitates at the grain boundaries changed the behavior of the equiaxed material to non-Newtonian (n= 2) at a pressure of ∼300 MPa, possibly because of a grain-boundary sliding mechanism; the tabular-grained material showed Newtonian diffusional creep under similar conditions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 84 (2001), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The failure mechanisms of air-plasma-sprayed ZrO2 thermal barrier coatings with various microstructures were studied by microscopic techniques after thermal cycling. The elastic modulus (E) and hardness (H) of the coatings were measured as functions of the number of thermal cycles. Initially, both E and H increased by ∼60% with thermal cycling because of sintering effects. However, after ∼80 cycles (0.5 h at 980°C), the accumulated damage in the coatings led to a significant decrease of ∼20% of the maximum value in both E and H. These results were correlated with stresses measured by a spectroscopic technique to understand specific damage mechanisms. Stress measurement and analysis revealed that the stress distribution in the scale was a complex function of local interface geometry and damage in the top coat. Localized variations in geometry could lead to variations in measured hydrostatic stresses from −0.25 to −2.0 GPa in the oxide scale. Protrusions of the top ZrO2 coat into the bond coat were localized areas of high stress concentration and acted as damage-nucleation sites during thermal and mechanical cycling. The net compressive hydrostatic stress in the oxide scale increased significantly as the scale spalled during thermal cycling.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary New dioxomolybdenum(VI) complexes [MoO2LD] (LH2=Schiff base derived from isonicotinylhydrazide and salicylaldehyde, 2-hydroxynaphthaldehyde and 2-hydroxyacetophenone and benzoylhydrazide and 2-hydroxyacetophenone; D=H2O, HCONMe2, C5H5NO, C4H8O or Me2SO) have been synthesized and characterized. The complexes contain acis-MoO2 moiety. The difference betweenv sym andv asymm of MoO2 is related to the basicity and ligand repulsion of the ligand (L) and the donor power of D. All the complexes decompose before melting and their thermal stability is in the order: C4H8O 〈 HCONMe2 〈 Me2SO 〈 C5H5NO 〈 H2O. The complexes are monomeric, non-electrolytes in solution in MeOH, MeCN and PhNO2 and are diamagnetic.
    Type of Medium: Electronic Resource
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