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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemistry of materials 2 (1990), S. 645-647 
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 19 (2000), S. 1477-1479 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 14 (1995), S. 1354-1356 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 30 (1995), S. 4076-4086 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Lithium silicate powders were prepared by several sol-gel routes. Starting solutions contained equimolar amounts of lithium and silicon, but single-phase lithium disilicate (Li2Si2O5) formed only when local stoichiometry was maintained through gelation and drying. Gels prepared from solutions containing LiNO3, tetraethylorthosilicate (TEOS), water and ethanol were visibly homogeneous, but on drying the local stoichiometry was upset by the recrystallization of LiNO3. Consequently, a lithium-rich phase (Li2SiO3) was the first to crystallize on heating with a lesser amount of Li2Si2O5 forming at a higher temperature. Solutions containing TEOS and lithium methoxide formed a precipitate when combined with a water/ethanol hydrolysis solution. The precipitate dissolved before gelation, but the resulting powders crystallized into a mixture of Li2SiO3 and Li2Si2O5. The relative amount of Li2Si2O5 could be increased by adding HNO3 to the hydrolysis solution and using lower water contents. Precipitation was avoided by partially hydrolysing TEOS before adding the lithium alkoxide; these powders crystallized directly into Li2Si2O5 after heating at 550 °C. Gel-derived powders prepared using an Li-Si methoxyethoxide solution also crystallized directly into Li2Si2O5.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 30 (1995), S. 6192-6204 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Lithium disilicate (Li2Si2O5) coatings were prepared by spin-coating alkoxide solutions on to substrates [Si, SiO2, polycrystalline (poly) Si, sapphire] and heating isothermally at 500–600 °C. The effects of solution chemistry, coating thickness and substrate type on crystallization behaviour and microstructure development were investigated using atomic force microscopy, X-ray diffraction and transmission electron microscopy. Amorphous dried coatings began to crystallize into Li2Si2O5 at 500–550 °C. Coatings prepared on Si substrates (with a thin native oxide) using Li-Si methoxyethoxide solution crystallized into microstructures with large grain sizes (ca. 2–5 μm diameter) as compared with the coating thickness (〈0.3 μm). Nucleation rate in these coatings could be increased (and hence transformation rate increased and grain size decreased) by: (1) adding H2PtCl6to the solution to act as nucleation agent; (2) increasing the thickness of the coating; or (3) using a crystalline substrate (sapphire or poly Si). Coatings prepared using Li-Si ethoxide solution had fine-grained microstructures (⩽0.5 μm diameter) for all substrates. Chemical heterogeneity in the ethoxide system may have increased nucleation rate. Nucleation rate in this system could be decreased by using partially hydrolysed tetraethylorthosilicate as the Si precursor. The relationship between solution chemistry and microstructure was used to tailor microstructures in multilayer coatings.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 33 (1998), S. 4423-4433 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Porous titania coatings were prepared by spin coating anhydrous titanium ethoxide–ethanol solutions in a controlled humidity atmosphere. Ti ethoxide reacted with atmospheric moisture during deposition, to form amorphous particles (approximately 200 nm), a dense layer or a combination of the two, depending on the processing conditions. Relatively humid atmospheres, low concentrations of Ti ethoxide in the coating solution and slow spinning rates favoured particle formation. These particulate coatings were typically composed of agglomerated particle clusters. Agglomeration could be prevented by adding hydroxypropyl cellulose to alkoxide solution to act as a steric stabilizer for newly formed particles. During thermal treatment, the coatings crystallized into the anatase phase and then transformed into the rutile structure at higher temperatures. The anatase–rutile transformation in porous coatings occurred over a range of 850–1150°C and strongly depended on microstructural features. More porous coatings with larger particle clusters transformed to rutile at lower temperatures. Tensile stress in the coating caused by constrained shrinkage inhibited the phase transformation. The substrate constraint slowed the transformation rate in coatings relative to free powder. Stress relief through rupture of particle cluster connections allowed transformation to occur at lower temperatures. © 1998 Kluwer Academic Publishers
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 25 (1990), S. 5007-5013 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Lead magnesium niobate powders and thin layers were formed from an alkoxide-based solution by sol-gel methods. The solution was synthesized by reacting a magnesium-niobium alkoxide solution with a lead acetate-based precursor solution. The effects of gelation conditions on the properties of the dried gel, and on the organic decomposition behaviour and crystalline phase development in gel-derived powders are reported. Gels prepared with greater molar ratios of water to alkoxide (3∶1) had the largest surface areas (130 m22 g−1) and required the lowest temperature (320 ° C) for organic removal. The perovskite phase first appeared at temperatures near 700 ° C, and developed at a faster rate in gels prepared with higher water contents. Approximately 95% developed after 1 h at 700 ° C, or 5 min at 775 ° C. Dielectric thin layers were prepared on platinum-coated silicon substrates by a multilayered spin-casting method. The perovskite phase formed most readily in the thin layers by a fast-firing treatment at 800 ° C. Microstructures and electrical properties are reported for the integrated thin layer dielectrics. Ferroelectric hysteresis loops were observed.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 1279-1290 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Industrial equipment for drying polymeric coatings normally consists of a series of zones, each with a controlled temperature and airflow. Drying of a polymer-solvent solution is strongly affected by the variation of diffusivity, solvent vapor pressure, and solvent activity with temperature and composition. The equations of mass transfer by diffusion and of heat transfer by conduction and radiation describe changes in composition and temperature within the shrinking coating. This system of equations is solved by Galerkin's method with finite element basis functions. The boundary conditions on dryer airflow and temperature change at the entrance to each zone. In a few test cases, the predictions show how evaporative cooling can slow drying in early zones where the coating temperature drops below the dryer temperature, whereas in later zones the coating temperature rapidly approaches the dryer temperature. Infrared heating can be used to reduce the extent of evaporative cooling. In the test cases and experiments, “blistering” occurs in later zones where high oven temperature causes the solvent partial pressure to rise; dryer parameters can be chosen to maintain solvent partial pressure just below ambient pressure in order to avoid “blistering” with least sacrifice of process speed. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 9
    Publication Date: 1995-12-01
    Print ISSN: 0022-2461
    Electronic ISSN: 1573-4803
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Published by Springer
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  • 10
    Publication Date: 1998-12-01
    Print ISSN: 1155-4339
    Electronic ISSN: 1764-7177
    Topics: Physics
    Published by EDP Sciences
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