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  • 1
    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: The effect of germanium oxide (GeO2) addition on the anatase-to-rutile phase transition was investigated by differential thermal analysis (DTA), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). TiO2 xerogels containing up to 20 mol% GeO2 were prepared by refluxing and hydrolyzing titanium tetraisopropoxide (TTIP) and germanium butoxide (GB) using nitric acid as a catalyst. The following occurred with increasing amounts of GeO2 in the xerogels: (i) the crystallization temperature of anatase increased from 410° to 565°C and the DTA temperature of the anatase-to-rutile phase transition increased from 676° to 977°C in 20 mol% GeO2-containing xerogel; (ii) the crystallite size of anatase became smaller; (iii) the lattice a-parameter of the anatase showed little change, but the c-parameter decreased up to 20 mol% GeO2; (iv) both the lattice a- and c-parameters of the rutile decreased monotonically. From these results, the added GeO2 is considered to become incorporated into the anatase structure. The following occurred with increasing anatase heating temperature: (i) the lattice c-parameter of the anatase increased gradually and approached the value of pure anatase; and (ii) the chemical composition of the xerogel surfaces, measured by XPS, showed an increase in GeO2 content, indicating the expulsion of GeO2 from the anatase to form an amorphous surface layer. The formation of this amorphous GeO2 surface layer is thought to play an important role in retarding the anatase-to-rutile phase transition by suppressing diffusion between the anatase particles in direct contact, and limiting their ability to act as surface nucleation sites for rutile, as in the case of SiO2 additions. However, GeO2 addition is less effective than SiO2 in retarding the phase transition.
    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 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 mechanism of mullite crystallization in Al2O3-SiO2 glass fibers with compositions of 49 and 69 mass% Al2O3 was investigated using isothermal methods. The activation energies (Ea) of the nucleation and nucleation-growth of mullite were obtained from the temperature dependence of the incubation times and rate constants of mullite formation, respectively. The formation of mullite in both glasses occurred in two stages. The amount of mullite increased very steeply in the first stage within very short firing time, whereas the increase was more gradual in the second stage. The Ea values for nucleation and nucleation-growth in the first stage were 864 and 1288 kJ/mol in the 49-mass%-Al2O3 glass fiber and 980 and 1138 kJ/mol in the 69-mass%-Al2O3 glass fiber, respectively. Arrhenius plots of the second-stage data showed that the slope ratios were different at temperatures below and above 1200°C. The Ea values at 〈1200°C were 1195 and 1099 kJ/mol in the 49- and 69-mass%-Al2O3 glass fibers, whereas those at 〉1200°C were 696 and 645 kJ/mol, respectively. Observation of the microstructures and crystallite-size data indicates that the crystallization of mullite proceeds via three different mechanisms: nucleation, nucleation–growth, and coalescence of mullite grains.
    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 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: This paper focused on the effects of various phases of SiO2 additives on the γ-Al2O3-to-α-Al2O3 phase transition. In the differential thermal analysis, the exothermic peak temperature that corresponded to the theta-to-α phase transition was elevated by adding amorphous SiO2, such as fumed silica and silica gel obtained from the hydrolysis of tetraethyl orthosilicate. In contrast, the peak temperature was reduced by adding crystalline SiO2, such as quartz and cristobalite. Amorphous SiO2 was considered to retard the γ-to-α phase transition by preventing γ-Al2O3 particles from coming into contact and suppressing heterogeneous nucleation on the γ-Al2O3 surface. On the other hand, crystalline SiO2 accelerated the α-Al2O3 transition; thus, this SiO2 may be considered to act as heterogeneous nucleation sites. The structural difference among the various SiO2 additives, especially amorphous and crystalline phases, largely influenced the temperature of γ-Al2O3-to-α-Al2O3 phase transition.
    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 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 effect on the γ-Al2O3-to-α-Al2O3 phase transition of adding divalent cations was investigated by differential thermal analysis, X-ray diffractometry, and surface-area measurements. The cations, Cu2+, Mn2+, Co2+, Ni2+, Mg2+, Ca2+, Sr2+, and Ba2+, were added by impregnation, using the appropriate nitrate solution. These additives were classified into three groups, according to their effect: (1) those with an accelerating effect (Cu2+ and Mn2+), (2) those with little or no effect (Co2+, Ni2+, and Mg2+), and (3) those with a retarding effect (Ca2+, Sr2+, and Ba2+). The crystalline phase formed by reaction of the additive with γ-Al2O3 at high temperature was a spinel-type structure in groups (1) and (2) and a magnetoplumbite-type structure in group (3). In groups (2) and (3), a clear relationship was found between the transition temperature and the difference in ionic radius of Al3+ and the additive (Δr): The transition temperature increased as Δr increased. This result indicates that additives with larger ionic radii are more effective in suppressing the diffusion of Al3+ and O2− in γ-Al2O3, suppressing the grain growth of γ-Al2O3, and retarding the transformation into α-Al2O3.
    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 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: The binding energy of Si 2p electrons and the kinetic energy of the Si(KLL) X-ray-excited state were measured by using X-ray photoelectron spectroscopy (XPS) and X-ray Auger electron spectroscopy (XAES), respectively, for silicates with SiO4 tetrahedra of various polymerization types. The resulting Si 2p XPS binding energies varied from 101.3 eV in merwinite (monomeric structure) to 103.4 eV in quartz and cristobalite (three-dimensional framework structure). A clear chemical-shift relation was observed, relating the polymerization structures of SiO4 tetrahedra to the plots of their Si 2p XPS binding energy versus the kinetic energy of their Si(KLL) XAES spectra. Thus, the structural state of the surface silicates in various substances can be deduced from this chemical-shift relationship.
    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 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 sintering behavior of green compacts, in which coarse alumina particles formed a skeletal structure and fine alumina and/or fine titania particles filled the voids of the skeletal structure, was investigated. Sinterability of the green compacts changed according to the titania content in the fine powder. The titania content of 33 mol% was the most effective for the densification. The volume expansion due to the aluminum titanate formation occurred in the voids of the skeletal structure, and the densification of the skeletal structure progressed more because the grain growth between the fine and coarse alumina particles did not proceed. As the titania content decreased, the densification did not progress more than that of the compact with 33 mol% titania content because the grain growth proceeded more. As the titania content increased, the expansion of the compacts was larger, and large grains were formed by the reaction between the titania and coarse alumina particles. Therefore, densification became difficult.
    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 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 effect of monovalent cation addition on the γ-Al2O3-to-α-Al2O3 phase transition was investigated by differential thermal analysis, powder X-ray diffractometry, and specific-surface-area measurements. The cations Li+, Na+, Ag+, K+, Rb+, and Cs+ were added by an impregnation method, using the appropriate nitrate solution. β-Al2O3 was the crystalline aluminate phase that formed by reaction between these additives and Al2O3 in the vicinity of the γ-to-α-Al2O3 transition temperature, with the exception of Li+. The transition temperature increased as the ionic radii of the additive increased. The change in specific surface area of these samples after heat treatment showed a trend similar to that of the phase-transition temperature. Thus, Cs+ was concluded to be the most effective of the present monovalent additives for enhancing the thermal stability of γ-Al2O3. Because the order of the phase-transition temperature coincided with that of the formation temperature of β-Al2O3 in these samples, suppression of ionic diffusion in γ-Al2O3 by the amorphous phase containing the added cations must have played an important role in retarding the transition to α-Al2O3. Larger cations suppressed the diffusion reaction more effectively.
    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 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: The formation of a poorly crystalline layer-lattice type of magnesium silicate has been demonstrated in mixtures of magnesium hydroxide with hydrated silicic acid that has been intimately combined via grinding and then aged at room temperature for six months. X-ray diffractometry, Fourier transform infrared spectroscopy, and 29Si solid-state magic-angle spinning nuclear magnetic resonance show the product to be similar to that which has been obtained from the same mixture via hydrothermal treatment at a temperature of 80°C for 24 h. This reaction does not occur to any appreciable extent when the silicic acid is replaced by silica gel, which suggests that the hydration water has an essential role, probably in the dissolution of the silica in the alkaline environment of the magnesium hydroxide.
    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 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 effect of SiO2 addition on the anatase-to-rutile phase transition was investigated by DTA, XRD, FTIR, and XPS. TiO2 xerogels containing SiO2 up to 20 mol% were prepared by mixing and hydrolyzing titanium tetraisopropoxide (TTIP) and tetraethylorthosilicate (TEOS) with HNO3 as a catalyst. With increased amounts of SiO2 in the xerogels, the following results were obtained: (1) the crystallization temperature of anatase increased from 415°C in pure TiO2 to 609°C in 20-mol%-SiO2-containing xerogel in the DTA curves; (2) the formation temperature of rutile, according to quantitative XRD analysis, increased with increased SiO2 content up to 5 mol% SiO2 but became constant at higher SiO2 contents; (3) the crystallinity of anatase became lower; and (4) the lattice parameter a of the anatase decreased slightly, but the parameter c decreased greatly up to 20 mol% SiO2. Although the added silicon atoms were considered from these results to be incorporated into the amorphous TiO2 and anatase structures, the 29Si MAS NMR spectra of the xerogels containing 10 mol% SiO2 showed only tetrahedral silicon, with no indication of silicon in octahedral coordination. When calcined at higher temperatures, the xerogel showed polymerization of the SiO4 tetrahedra in the NMR spectra and the Si–O–Si vibration in the FTIR spectra. The chemical composition of the xerogel surfaces, measured using XPS, showed increased SiO2 content with increased calcining temperature, indicating the expulsion of silicon from inside the particles to form an amorphous SiO2 surface layer. The formation of this amorphous SiO2 surface layer was considered to be important in retarding the anatase-to-rutile phase transition by suppressing diffusion between anatase particles in direct contact and limiting their ability to act as surface nucleation sites for rutile. These effects of silicon additions were similar to those observed in the γ-Al2O3- to-α-Al2O3 transition.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 170-172 (Oct. 1994), p. 385-390 
    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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