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  • 1
    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: Monolithic polymer-derived Si-C-N ceramics were processed by blending an oligomeric Si-C-N precursor (liquid polysilazane) with 70 vol% of crosslinked or pyrolyzed Si-C-N powder particles, which were obtained from the same liquid precursor preheated at 300° or 1000°C, respectively. Powder compacts subsequently were annealed at 300°C to crosslink the liquid precursor acting as a binder between the powder particles, thus yielding monolithic green bodies. Heat treatment at 1540°C was performed to initiate crystallization in the various samples. Microstructure development and, in particular, crystallization behavior were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and preliminary nuclear magnetic resonance (NMR) spectroscopy. The material containing 300°C polymer powder (with oligomeric binder, also crosslinked at 300°C) revealed a homogeneous amorphous microstructure after exposure to temperatures of 1540°C. In contrast, the specimen containing powder particles preheated at 1000°C exhibited a high volume fraction of SiC crystallites within regions that were previously filled by the binder; however, the Si-C-N powder particles themselves remained amorphous. SEM observations as well as XRD studies showed the formation of idiomorphic SiC and Si3N4 crystallites on specimen surfaces as well as along internal crack walls. This finding suggested that vapor-phase reactions at the surface were involved in the formation of crystalline phases at temperatures 〉1250°C. Moreover, NMR spectroscopy data indicated a phase separation process, implying structural rearrangement prior to crystallization.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    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: A ceramic matrix for carbon-fiber-reinforced ceramic-matrix composites (CMCs) has been developed from poly-siloxane/boron mixtures. Complex geometries can be realized by using standard technologies of fiber-reinforced polymer composites. On pyrolysis, the polymer—filler mixture is converted to a ceramic matrix, consisting of silicon carbide, boron carbide, boron nitride, and a silicon oxycarbide (SiOC) glass, without reacting with the carbon fiber. Because of the large volume increase of the boron filler on nitridation (142 vol%), no multiple reinfiltration of the structure is necessary to achieve a dense matrix. Tensile strength and interlaminar shear strength exhibit maxima at a pyrolysis temperature of 1300°3C, where extensive fiber pullout is observed. Thermodynamic calculations have been used to evaluate the theoretical qualitative and quantitative phase compositions at equilibrium. Thermoanalytical (thermogravimetry—mass spectroscopy) and structural analysis (X-ray diffractometry) have shown a satisfying coherence with respect to the condensed phases, whereas deviations have been noted with respect to the composition of the gas phase.
    Type of Medium: Electronic Resource
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  • 3
    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: Monolithic mullite with low sintering shrinkage was synthesized from polymer/filler blendsMthat is, siloxane/alumina (siloxane/Al2O3) (and siloxane/aluminum (siloxane/Al)) mixtures. The synthesis was based on a reaction-bonding process of amorphous silica, which formed when the siloxane was oxidized, with Al2O3 (or oxidized aluminum filler) at temperatures 〉1250°C. Thermodynamic calculations were used to calculate the phase composition at equilibrium. Thermoanalytical, infrared-spectroscopic, and microscopic techniques were applied to reveal the microstructural evolution. The corresponding volume changes were used to evaluate the linear shrinkage, based on the quantitative phase assemblage.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 14 (1999), S. 69-74 
    ISSN: 1573-4846
    Keywords: sol-gel ; silicon oxycarbide glass ; high temperature stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The high temperature stability of sol-gel-derived SiOC glasses has been investigated in order to understand the role played by the presence of a free-carbon phase in the amorphous oxycarbide network. Therefore, pure and excess free-carbon containing SiOC glasses have been prepared from hybrid gels and used for the high temperature stability experiments. Moreover, the possible effects of the sample size with respect to local kinetics and thermodynamics and of the testing environment have also been investigated. Results show that all these parameters play a crucial role in defining the high temperature behavior of SiOC glasses.
    Type of Medium: Electronic Resource
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