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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 233-234 (Oct. 1996), p. 287-294 
    ISSN: 1662-9752
    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
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 317-318 (Aug. 2006), p. 487-490 
    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
    Notes: Polymer impregnation pyrolysis method (PIP method) has some advantages to fabricateSiC fiber /SiC composite with large or complex form. However polymer derived SiC containssome amount of excess carbon and porosity. In particular the excess carbon is easy to be oxidizedin air at high temperature. Therefore reliability of the composite is not sufficient for long term use,because the oxidized matrix makes strong bonding between the fiber and the matrix. In this study,TiO2 as a reactive filler was added into polymer to consume the excess carbon by chemical reaction.Polycarbosilane (PCS) was used as a precursor polymer to synthesize a SiC matrix. It wasconfirmed that TiO2 was formed TiC on reaction with PCS over 1673 K by preliminary study. SiCfiber, Hi-Nicalon®, was used as reinforcement. Al2O3 powder was coated on surface of SiC fiberas interface layer of fiber/matrix. TiO2 added PCS/hexane solution was compounded with thefiber tow by filament winding. SiC fiber/SiC composite was synthesized at 1673 K for 3.6 ks inAr. The composite was densified by reinfiltration of TiO2 added PCS solution and pyrolysis at1673 K. Though densification behavior of the composite with TiO2 is slower than compositewithout TiO2, it was suggested that composition of synthesized SiC is close to stoichiometric one byapparent density. Fracture behavior of the composite indicated that addition of TiO2 was increasebonding strength between fiber and matrix. Bending strength of composite was increased afteroxidation test at 1473 K for 360 ks in air atmosphere
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 317-318 (Aug. 2006), p. 513-516 
    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
    Notes: Alumina/zirconia nano-composite coating was fabricated by plasma spraying usingagglomerated feedstock from fine powders of about 100 nm. The coating was consisted of fineγ-alumina and zirconia crystals with size of several nano meter and some amorphous boundary layers.The amorphous phase was crystallized and disappeared after heat treatment at 930°C. However, thecrystallite size was kept under 50 nm even after 1500°C-100hr heating, so the alumina-zirconianano-composite showed good thermal stability against the grain growth
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 90 (2001), S. 462-465 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Spark plasma sintering (SPS) was applied for preparing dense Ca2.75Gd0.25Co4O9 ceramics, and their thermoelectric properties were investigated from room temperature to 700 °C in air. The SPS process was effective in obtaining dense Ca2.75Gd0.25Co4O9 ceramics, typically 98% of the theoretical x-ray density, with lower resistivity, without any degradation of the thermoelectric power. The power factor and figure of merit of the spark plasma sintered samples attain 4.8×10−4 W m−1 K−2 and ZT=0.23 at 700 °C, respectively. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 78 (2001), S. 3627-3629 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: An oxide thermoelectric device was fabricated using Gd-doped Ca3Co4O9 p-type legs and La-doped CaMnO3 n-type legs on a fin. The power factors of p legs and n legs were 4.8×10−4 Wm−1 K−2 and 2.2×10−4 Wm−1 K−2 at 700 °C in air, respectively. With eight p–n couples the device generated an output power of 63.5 mW under the thermal condition of hot side temperature Th=773 °C and a temperature difference ΔT=390 °C. This device proved to be operable for more than two weeks in air showing high durability. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 76 (2000), S. 2385-2387 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Bi2Sr2Co2O9 (BC-2202) polycrystalline materials with a layered structure have been prepared by partial melting. The chemical compositions of the samples are Bi2Sr2Co2Ox (2202), Bi1.8Sr2Co2Ox (Bi-1.8), and Bi2Sr1.8Co2Ox (Sr-1.8). All three samples are p-type conductors. The electric properties, namely, the Seebeck coefficient (S) and electric resistivity (ρ), of the samples are dependent on chemical composition. The S values increase with temperature at T〉673 K and, at 973 K, reach 100, 110, and 150 μV K−1 for the 2202, the Bi-1.8, and the Sr-1.8 samples, respectively. Thermal conductivity (κ) for all samples is lower than for ordinary conducting oxides. The figure of merit (Z) increases with temperature for all samples. Z values at 973 K are 0.77×10−4, 0.61×10−4, and 2.0×10−4 K−1 for the 2202, Bi-1.8, and Sr-1.8 samples, respectively. The thermoelectric properties depend on the chemical composition of the BC-2202 phase. The BC-2202 material thus appears to be a promising thermoelectric material due to its high performance at high temperature (∼1000 K). © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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