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  • American Ceramics Society  (2)
  • 1995-1999  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 80 (1997), 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: Ultrafine 5.5 mol% CeO2—2 mol% YO1.5ZrO2 powders with controllable crystallite size were synthesized by two kinds of coprecipitation methods and subsequent crystallization treatment. The amorphous gel produced by ammonia coprecipitation and hydrothermal treatment at 200°C for 3.5 h results in an ultrafine powder with a surface area of 206 m2/g and a crystallite size of 4.8 nm. The powder produced by urea hydrolysis and calcination exhibits a purely tetragonal phase. In addition, the powders crystallized by hydrothermal treatment exhibit high packing density and can be sintered at lower temperature (,1400°C) with nearly 100% tetragonal phase achieved.
    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 81 (1998), 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 final phases of zirconia powders depend on the synthesis method employed, and the amounts of stabilizer present. In this study, ceria- and yttria-doped zirconia powders were prepared by urea hydrolysis and subsequent hydrothermal treatment. The amount of tetragonal (t) vs monoclinic (m) phase in the powders increased with increasing stabilizer content, while the tetragonal phase size decreased and the microstrain of t crystals remained unchanged. The thermal degradation behavior of the metastable t phase in zirconia containing a low CeO2 or YO1.5 doping level was explored during aging treatment by means of X-ray line profile broadening analysis. Both ultrafine yttria- and ceria-doped zirconia powder pellets exhibit isothermal t→m transformation after aging at 900°C for various times. It is argued that a crystallite size effect, rather than the dopant valence, dictates the occurrence of the t→m transformation in ultrafine zirconia powders. The change in crystallite sizes of both t and m phases during aging depends significantly on the amount of stabilizer, aging time, and mechanism of t→m phase transformation. However, the change of microstrain in both t and m phases is related to the amount of stabilizers present and the matrix constraints.
    Type of Medium: Electronic Resource
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