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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 530-531 (Nov. 2006), p. 532-537 
    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
    Notes: In this work, SiC ceramics were prepared by liquid phase sintering using 10 wt.% of AlNand Y2O3 mixtures in the proportion of 4:1 and 2:3 as additives Sintering was done in a graphiteresistance heated furnace at 2080oC under 0.2 MPa N2 atmosphere for 1h. Part of the samples wasfurther heat-treated at 2000oC for 4h to allow grain growth. The microstructures of the sinteredsamples were analyzed using polished and plasma etched surfaces. Furthermore, relative densities,weight loss during sintering and SiC-polytype distributions are reported
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 591-593 (Aug. 2008), p. 616-619 
    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
    Notes: In this work, silicon carbide ceramics were developed by liquid phase sintering usingAlN-Y2O3 as additive. Two compositions were obtained using SiC powders and different contentsof AlN-Y2O3. The powders were mixed/homogeneizated and subsequently dried anddeagglomerated. Powder mixtures were compacted by cold isostatic pressing. Samples weresintered at 2080oC, for 1h, under 0.2 MPa-N2 atmosphere. Sintered samples were characterized byX-Ray diffraction and density. The oxidation behavior was investigated and related to thedensification and additive-content. Samples were submitted to the tests at 1200, 1300 or 1400oC, inair for 120 hours. Weight gain of the samples is plotted as function of the exposure time, obtainingthe evolution of the oxidation on the surface of the samples. Based on the results, the parabolicoxidation content (kp) and activation energy were determined. The results indicate that the samplespresent parabolic behavior in all conditions. The activation energy results indicate that thephenomena of diffusion of oxygen ions into the oxide layer and interfacial reactions between oxidelayer and intergranular phase are the responsible for oxidation mechanism
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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