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  • 1995-1999  (3)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 115 (Sept. 1995), p. 167-180 
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: 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 32 (1997), S. 4655-4660 
    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 The recycling of toxic goethite waste, originated in the hydrometallurgy of zinc ores, in glass-ceramic matrices has been studied. Oxide compositions suitable to form glasses were prepared by mixing the goethite waste with granite scraps and glass cullet, yielding the following oxide composition (wt%): SiO2, 44.6; Al2O3, 3.3; Fe2O3, 25.5; MgO, 1.6; CaO, 4.5; Na2O, 5.9; PbO, 3.1; ZnO, 6.5; K2O, 1.0; TiO2, 2.0; other 2.0. By proper addition of carbon powder, the initial Fe3+/Fe2+ ratio (12) of glasses melted in air at 1450°C was approximated to the stoichiometric value of magnetite (2) to obtain high nucleation and crystallization rates. The heat treatment of iron supersaturated goethite glasses above 630°C led to the formation of magnetite nuclei with a high tendency to grow and coalesce with time. The crystallization of pyroxene, occurring on the magnetite crystals above 800°C, was found to be influenced by the nucleation period, so that the highest crystalline volume fraction, Vf (0.80–0.85), was obtained for 90–120 min nucleation time at 670°C and 120 min crystallization at 860°C.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 33 (1998), S. 3969-3973 
    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 High-quality bulk ZnGa2O4 has been synthesized from equimolar mixtures of ZnO and Ga2O3 by the conventional solid-state method. For the first time, the sample has been characterized in detail to confirm the formation of pure single phase of spinel ZnGa2O4. The formation of ZnGa2O4 has been confirmed by sintering the mixtures of ZnO and Ga2O3 at different temperatures, ranging from 900–1200 °C. It is observed that the single phase of ZnGa2O4 has been formed at and above 1000 °C sintering temperature for 24 h. The crystallinity and phase formation of this single phase has been confirmed by X-ray diffraction. X-ray photoelectron spectroscopic studies have been carried out for bulk ZnGa2O4 sintered at 1000 °C for 24 h which showed 14% Zn, 28% Ga and 58% O, indicating stoichiometric ZnGa2O4. A new parameter, the energetic separation between the Zn 2p3/2 and Ga 2p3/2 peaks, has been used as a sensitive tool to distinguish between a complete formation of ZnGa2O4 compound and a mixture of ZnO and Ga2O3 powders. Surface morphology studies by scanning electron microscopy reveal that the formation of ZnGa2O4 takes place in mosaic rod-like structure. The purity of the compound has also been checked by the energy dispersive X-ray method, indicating the absence of foreign ions and the ratio of zinc to gallium has been calculated and found to be 1 : 2, indicating stoichiometric ZnGa2O4.
    Type of Medium: Electronic Resource
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