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  • 1
    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 different short-chained carboxylic acids, formic, acetic, and propionic acid, were compared as additives to increase the green strength of wet particle networks produced with the direct coagulation casting process, which allows the internal coagulation of a suspension. Small acid additions do not alter the favorable low viscosity of the stabilized slurry, and yet increase the compressive strength of wet coagulated bodies. The strengthening effect increases with increasing chain length of the carboxylic acid. The maximum effect was observed upon addition of propionic acid (0.3 wt% to alumina), which resulted in a sixfold increase in compressive strength of wet coagulated bodies compared with that without propionic acid.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 85 (2002), 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: This paper proposes a novel direct casting method of alumina suspensions using alginic acid salt and the coagulation agent hydroxyaluminum diacetate (HADA). These two compounds allowed the consolidation of alumina suspensions through a simultaneous time-delayed physical and chemical gelation process. The physical gel was formed by the gradual release of aluminum and acetate ions from the HADA in water, while the chemical gel originated from the cross-linking of alginate molecules by the polyvalent aluminum ions. Wet alumina green bodies displayed enhanced mechanical properties with the addition of minimal contents of organic material (〈0.1 wt%).
    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 84 (2001), 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: Alkali-swellable thickeners (ASTs) such as Acusol 820 and Acusol 830, as well as poly(acrylic acid) homopolymers of various molar mass, have been used as additives in aqueous electrostatically stabilized alumina suspensions. These suspensions have been destabilized by internal enzyme-catalyzed reactions (a direct coagulation casting process) to form viscoelastic solids. The ASTs increase the strength and modulus of the wet green bodies on coagulation. The effect of their molecular architecture on the mechanical properties of wet particulate networks has been studied. At low pH (pH 4.5), ASTs are small insoluble polymer particles that have only minor influence on the low viscosity of the high-solids-loading suspensions. After shifting the pH toward the isoelectric point of α-Al2O3, the suspension coagulates and the AST polymer particles swell, thereby increasing the compressive strength and modulus of the alumina-particulate wet green bodies. The presence of small amounts of ASTs (0.4 wt%, based on the solids loading) results in a 10-fold increase in the strength of the wet green bodies. The compressive strength of the wet green bodies that contain ASTs correlates with the size of the expanded AST molecules at pH 9. A possible explanation is that swelling of the AST particles locally decreases the interparticle distance, which leads to increased van der Waals forces between the ceramic particles.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 84 (2001), 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 aim of the present work is the preparation of thin (〈20 μm) zirconia layers on porous substrates with the electrophoretic deposition process. The preparation was completed with a cosintering step of substrate and layer. Through adjustment of shrinkage and the shrinkage rate of the deposited zirconia layer on the presintered porous substrate, thin, dense layers without cracks were prepared. A method for direct control of the layer thickness during the electrophoretic deposition process was developed. The solid oxide fuel cell application with porous anode substrates and thin zirconia electrolytes was chosen to demonstrate the potential of the electrophoretic deposition process.
    Type of Medium: Electronic Resource
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  • 5
    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: Direct coagulation casting is a novel near-net-shape method for forming ceramic green bodies from homogenous high-solids-loaded particle suspensions. It is based on the principle of the in situcoagulation of a powder suspension via a reaction-rate-controlled internal-enzyme(urease)-catalyzed reaction after casting. Low-viscosity (〈3 Pas) suspensions with a high solids loading (〉62 vol%) of SiC, boron, and carbon powder mixtures with a high surface area (〉7-10 m2/g) have been prepared at pH = 10. Salt ions (up to 1-2 mol/L) are created by the urease-catalyzed decomposition of urea, to destabilize the suspensions. The coagulation kinetics and the strength of the wet green bodies have been investigated. The reaction rate is strongly dependent on the temperature (in the range of 5°-30°C) and the enzyme concentration (for the range of 4-16 units/g SiC) and is independent of the substrate (urea) concentration for urea concentrations of 〈2 wt%, based on the powder content. The resulting green bodies show no shrinkage during coagulation and 1%-2% linear shrinkage during drying. The compressive strengths of the wet green bodies are as high as 60 kPa and increase as the coagulation time increases. The wet green strength of the coagulated suspensions scales with the solids content, according to a power law with an exponent of 11, in the range of 56-61 vol% solids content. The possibilities of fabricating high-solids-containing complex SiC green and sintered components with homogenous microstructures and high sintered densities are demonstrated.
    Type of Medium: Electronic Resource
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  • 6
    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: The Ag-Bi-O system has been experimentally studied using differential thermal analysis (DTA) and scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDX), and thermodynamically optimized. The temperatures of the eutectic, monotectic, and Bi2O3 allotropic transformations have been measured in N2, in air, and in O2 by DTA. There are no ternary phases stable at ambient pressure. Presently measured transformation temperatures have been combined with existing oxygen activity measurements in the metal liquid to optimize thermodynamic parameters describing the liquid phase. The resulting fit is excellent. EDX measurements of the composition in the oxide liquid have a rather low precision but confirm the thermodynamic optimization. However, some uncertainties remain concerning the liquid composition at the eutectic transformation and the shape of the miscibility gap at higher temperatures.
    Type of Medium: Electronic Resource
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  • 7
    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: Phase equilibria in the Ag-CuO-Cu2O system were experimentally determined using thermal analysis, and structural and compositional studies. Three reactions were observed in air: (1) L1= CuO + Ag, (2) L2= CuO + L1, and (3) Cu2O = CuO + L2. The evolution and absorption of oxygen accompanied these reactions. At oxygen partial pressures below 0.02 bar, the reactions L1= Cu2O + Ag and L2= Cu2O + L1 were found. Based on isobaric projections in the Ag-CuO-Cu2O system, two invariant reactions, L1= CuO + Cu2O + Ag and L2= CuO + Cu2O + L1, were deduced.
    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 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: The phase relations in the silver-strontium-copper-oxygen (Ag-Sr-Cu-O) and silver-calcium-copper-oxygen (Ag-Ca-Cu-O) systems were studied in oxygen, air, and nitrogen environments, using differential thermal analysis and energy-dispersive X-ray spectrometry. The presence of silver reduces the melting temperature of the oxide liquid to a monotectic in the strontium- and calcium-containing systems by 62 and 82 K, respectively (to 1222 and 1244 K, respectively) in oxygen. The oxide liquid dissolves silver (up to a metallic ratio of 0.17) in the Ag-Sr-Cu-O system in oxygen at a temperature slightly higher than that required for monotectic reaction. In the Ag-Ca-Cu-O system, the silver content has been measured to be 0.29 (metallic ratio). The oxide systems have been optimized using the experimental data from monotectics and those from lower-order systems that have been published previously. This work is part of a project to evaluate the phase relations within the silver-bismuth-strontium-calcium-copper-oxygen (Ag-Bi-Sr-Ca-Cu-O) system and, in particular, to focus on the influence of silver on the phase equilibria around the superconducting phases during partial-melt processing.
    Type of Medium: Electronic Resource
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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: An assessment of the silver–oxygen system has been made, and a consistent set of thermodynamic parameters has been optimized. The calculated thermodynamic properties and phase relations are in good agreement with the experimental data. Ag2O is the only phase that is commonly found within the system. In air, it decomposes to silver and oxygen gas at 420 K. There is a eutectic between silver and Ag2O at a temperature of 804 K, an oxygen partial pressure (PO2) of 526 bar (5.26 × 107 Pa), and an oxygen mole fraction in the liquid phase of 0.25. Uncertainties remain on the Ag2O liquidus for PO2 〉 108 Pa. An ionic two-sublattice model has been used to describe the liquid phase. This work is part of a study of interactions between compounds from the bismuth-strontium-calcium-copper-oxygen system and silver.
    Type of Medium: Electronic Resource
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  • 10
    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 experimental data on the oxide part of the Bi-Ca-O system have been reviewed, and an optimized thermodynamic description is presented. There are six known stable ternary oxide phases, two of which show considerable solid-solution ranges. At least two phases—delta–Bi2O3 and the rhombohedral ß-phase–are good oxygen-ion conductors. Because all oxide phases are found on the Bi2O3–CaO line, the Bi2O3-CaO system can be treated as a true binary system. Most experimental data are in reasonable agreement with each other; however, there are fairly large uncertainties on the extension of the solid-solution phases and on the thermodynamic properties.
    Type of Medium: Electronic Resource
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