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  • 1
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 87 (2004), 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 volatility of alumina in high-temperature water vapor was determined by a weight loss technique. Sapphire coupons were exposed at temperatures between 1250° and 1500°C, water partial pressures between 0.15 and 0.68 atm in oxygen, a total pressure of 1 atm, and flowing gas velocities of 4.4 cm/s. The water vapor pressure dependence of sapphire volatility was consistent with Al(OH)3(g) formation. The enthalpy of reaction to form Al(OH)3(g) from sapphire and water vapor was determined to be 210 ± 20 kJ/mol, comparing favorably to other studies. Microstructural examination of tested sapphire coupons revealed surface rearrangement consistent with a volatilization process.
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  • 2
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 87 (2004), 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: Stress-rupture tests were conducted in air, under vacuum, and in steam-containing environments to identify the failure modes and degradation mechanisms of a carbon-fiber-reinforced silicon carbide (C/SiC) composite at two temperatures, 600° and 1200°C. Stress-rupture lives in air and steam-containing environments (50–80% steam with argon) are similar for a stress of 69 MPa at 1200°C. Lives of specimens tested in a 20% steam/argon environment were about twice as long. For tests conducted at 600°C, composite life in 20% steam/argon was 30 times longer than life in air. Thermogravimetric analysis of the carbon fibers was conducted under conditions similar to the stress-rupture tests. The oxidation rate of the fibers in the various environments correlated with the composite stress-rupture lives. Examination of the failed specimens indicated that oxidation of the carbon fibers was the primary damage mode for specimens tested in air and steam environments at both temperatures.
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  • 3
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 86 (2003), 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: Two commercially available additive-containing silicon nitride materials were exposed in four environments which ranged in severity from dry oxygen at 1 atm pressure, and low gas velocity, to an actual turbine engine. Oxidation and volatilization kinetics were monitored at temperatures ranging from 1066° to 1400°C. The main purpose of this paper is to examine the surface oxide morphology resulting from the exposures. It was found that the material surface was enriched in rare-earth silicate phases in combustion environments when compared with the oxides formed on materials exposed in dry oxygen. However, the in situ formation of rare-earth disilicate phases offered little additional protection from the volatilization of silica observed in combustion environments. It was concluded that externally applied environmental barrier coatings are needed to protect additive-containing silicon nitride materials from volatilization reactions in combustion environments.
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  • 4
    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: A high-pressure sampling mass spectrometer was used to detect the volatile species formed from SiO2 at temperatures between 1200° and 1400°C in a flowing water vapor/oxygen gas mixture at 1 bar total pressure. The primary vapor species identified was Si(OH)4. The fragment ion Si(OH)3+was observed in quantities 3 to 5 times larger than the parent ion Si(OH)4+. The Si(OH)3+ intensity was found to have a small temperature dependence and to increase with the water vapor partial pressure as expected. In addition, SiO(OH)+, believed to be a fragment of SiO(OH)2, was observed. These mass spectral results were compared to the behavior of silicon halides.
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  • 5
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 86 (2003), 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: At high temperatures, SiC and Si3N4 react with water vapor to form a SiO2 scale. SiO2 scales also react with water vapor to form a volatile Si(OH)4 species. These simultaneous reactions, one forming SiO2 and the other removing SiO2, are described by paralinear kinetics. A steady state, in which these reactions occur at the same rate, is eventually achieved. After steady state is achieved, the oxide found on the surface is a constant thickness, and recession of the underlying material occurs at a linear rate. The steady-state oxide thickness, the time to achieve steady state, and the steady-state recession rate can be described in terms of the rate constants for the oxidation and volatilization reactions. In addition, the oxide thickness, the time to achieve steady state, and the recession rate also can be determined from parameters that describe a water-vapor-containing environment. Accordingly, maps have been developed to show these steady-state conditions as a function of reaction rate constants, pressure, and gas velocity. These maps can be used to predict the behavior of SiO2 formers in water-vapor-containing environments, such as combustion environments. Finally, these maps are used to explore the limits of the paralinear oxidation model for SiC and Si3N4.
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  • 6
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 86 (2003), 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: Three Si3N4 materials were exposed to dry oxygen flowing at 0.44 cm/s at temperatures between 1200° and 1400°C. Weight change was measured using a continuously recording microbalance. Parabolic kinetics were observed. When the same materials were exposed to a 50% H2O–50% O2 gas mixture flowing at 4.4 cm/s, all three types exhibited paralinear kinetics. The material was oxidized by water vapor to form solid SiO2. The protective SiO2 was in turn volatilized by water vapor to form primarily gaseous Si(OH)4. Nonlinear least-squares analysis and a paralinear kinetic model were used to determine parabolic and linear rate constants from the kinetic data. Volatilization of the protective SiO2 scale could result in accelerated consumption of Si3N4. Recession rates under conditions more representative of actual combustors were compared with the furnace data.
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  • 7
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 86 (2003), 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
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 83 (2000), 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 oxidation kinetics of CVD SiC were measured by thermogravimetric analysis (TGA) in a 4H2·12H2O·10CO·7CO2·67N2 gas mixture flowing at 0.44 cm/s at temperatures between 1300° and 1450°C in fused quartz furnace tubes at 1 atm total pressure. The SiC was oxidized to form solid SiO2. At ≥1350°C, the SiO2 was in turn volatilized. Volatilization kinetics were consistent with the thermodynamic predictions based on SiO formation. These two simultaneous reactions resulted in overall paralinear kinetics. A curve fitting technique was used to determine the linear and parabolic rate constants from the paralinear kinetic data. Volatilization of the protective SiO2 scale resulted in accelerated consumption of SiC. Recession rates under conditions more representative of actual combustors were estimated from the furnace data.
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  • 9
    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: The oxidation kinetics of CVDSiC were monitored by thermogravimetric analysis (TGA) in a 50% H2O/50% O2 gas mixture flowing at 1.4 cm/s for temperatures between 1200” and 1400°C. Paralinear weight change kinetics were observed as the water vapor oxidized the SiC and simultaneously volatilized the silica scale. The long-term degradation rate of SiC is determined by the volatility of the silica scale. Rapid SiC surface recession rates were estimated from these data for actual aircraft engine combustor conditions.
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  • 10
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 82 (1999), 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: In combustion environments, volatilization of SiO2 to Si-O-H(g) species is a critical issue. Available thermochemical data for Si-O-H(g) species were used in the present study to calculate boundary-layer-controlled fluxes from SiO2. Calculated fluxes were compared to volatilization rates of SiO2 scales grown on SiC, which were measured in a high-pressure burner rig, as reported in Part I of this paper. Calculated volatilization rates also were compared to those measured in synthetic combustion gas furnace tests. Probable vapor species were identified in both fuel-lean and fuel-rich combustion environments, based on the observed pressure, temperature, and velocity dependencies, as well as on the magnitude of the volatility rate. Water vapor was responsible for the degradation of SiO2 in the fuel-lean environment. SiO2 volatility in fuel-lean combustion environments was attributed primarily to the formation of Si(OH)4(g), with a small contribution of SiO(OH)2(g). Reducing gases such as H2 and/or CO, in combination with water vapor, contributed to the degradation of SiO2 in the fuel-rich environment. The model to describe SiO2 volatility in a fuel-rich combustion environment gave a less satisfactory fit to the observed results. Nevertheless, it was concluded-given the known thermochemical data-that SiO2 volatility in a fuel-rich combustion environment is best described by the formation of SiO(g) at 1 atm total pressure and the formation of Si(OH)4(g), SiO(OH)2(g), and SiO(OH)(g) at higher pressures. Other Si-O-H(g) species, such as Si2(OH)6, may contribute to the volatility of SiO2 under fuel-rich conditions; however, complete thermochemical data are unavailable at this time.
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