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  • 1
    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: Phase equilibria in the Bi2O3-CaO system have been examined over the temperature range of 650°-1050°C in oxygen at a pressure of 1 atm. Direct electron microprobe analysis has been used to determine the compositions of several phases with fixed Bi:Ca ratios and to determine the extents of compositional ranges of the three solid solutions in the system. The face-centered-cubic solid solution (FCCss) phase extends from pure Bi2O3 to a maximum CaO content of 27 mol% at 816°± 4°C. In the bismuth-rich portion of the diagram, the FCCss phase is replaced by monoclinic Bi2O3 (which dissolves essentially no CaO) and a rhombohedral solid solution (Rhss) phase with 12 mol% CaO. The eutectoid is located at 6 mol% CaO and 684°± 3°C. A calcium-rich FCCss phase also coexists at a eutectoid with a Rhss phase (23.5 mol% CaO) and Bi2CaO4 at 766°± 3°C. There are two two-phase regions between the FCCss and Rhss phases that have a closure temperature that is estimated to be ∼840°C. The Rhss phase exists between these two-phase regions. The minimum CaO content of this solid solution is 12 mol%, and its maximum CaO content is 23.5 mol%; however, the extent of solid solution is highly temperature dependent at 〉700°C. All liquids with 0-23 mol% CaO may coexist with a FCCss phase. The stability field of the rhombohedral phase does not reach the solidus, and there is a thermal maximum on the liquidus that is estimated at ∼880°C at which a FCCss phase and a liquid phase, each with 17 mol% CaO, coexist. Liquid with 23 mol% CaO, a FCCss phase, and a body-centered-cubic solid solution (BCCss) phase with 27 mol% CaO coexist at a eutectic near 866°C. The BCCss phase has a maximum composition range of 27-42 mol% CaO, although the range is dependent on temperature. At temperatures below 816°± 4°C, the BCCss phase is replaced by a FCCss phase and Bi6Ca4O13. At 970 ± 3°C, the BCCss phase with 42 mol% CaO melts incongruently to CaO and a liquid. Thus, only three phases-FCCss, BCCss, and CaO-coexist with liquids in the Bi2O3-CaO system. However, several other phases are identified in the subsolidus region: Bi14Ca5O26, which is replaced by a Rhss phase and Bi2CaO4 at 745°± 5°C; Bi2CaO4, which decomposes to a FCCss phase and Bi6Ca4O13 at 776°± 3°C; Bi6Ca4O13, which is replaced by a BCCss phase and Bi2Ca2O5 at ∼878°± 3°C; and Bi2Ca2O5, which decomposes to a BCCss phase and CaO at 931°± 5°C.
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 199 (1994), S. 425-432 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 264-268 (May 2004), p. 2275-2278 
    ISSN: 1013-9826
    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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  • 4
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Advances in science and technology Vol. 51 (Oct. 2006), p. 60-63 
    ISSN: 1662-0356
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Natural Sciences in General , Technology
    Notes: SiC nanofibers were prepared by using polymer blend and melt-spinning techniques.Polycarbosilane (PCS) as a SiC precursor polymer was dispersed finely in novolac-phenolic resin(PF) as a carbon precursor polymer with a ratio of PCS/PF=3/7. The polymer blend was melt-spuncontinuously. The fibers were then soaked in an acid solution in order to stabilize them (to convertinto an infusible state) and finally heat-treated at 1000°C. The resulting fibers consisted ofPF-derived carbon matrix including elongated nanofibers derived from PCS. Finally, the fibers wereoxidized with nitric acid to remove the carbon matrix, and the released nanofibers were collectedwith a membrane filter. The resulting nanofibers were several 100 nm in diameter and 100 μm ormore in length. They were amorphous and contained a large amount of oxygen. A part of thenanofibers was further heated to 1500°C in a graphite tube resistance furnace, resulting incrystallization into β-SiC. The behaviors were quite similar to those of a commercially availableSiC fibers derived from PCS. In order to obtain optimum conditions, the processes were examined
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 46 (1996), S. 521-528 
    ISSN: 1572-8943
    Keywords: methacrylamide-montmorillonite intercalation ; thermal stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermal stability of methacrylamide intercalated octadecylammonium montmorillonite (OD-M/MA) is limited by rapid desorption of methacrylamide (MA) at 140°C. It was improved by γ-irradiation. The irradiation intercalation complex OD-M/MA γ shows significant shift of the whole desorption process towards higher temperatures. However, part of the adsorbed organic material is released at 50°C signalizing presence of some volatile fractions. Decomposition products of the intercalated material and long-chain alkylamides in the acetone extract indicate complex reactions between MA and octadecylammonium chains. An additional swelling of the silicate structure occurs after γ-ray initiation and is probably related to the reaction products with a certain degree of cross-linking in the interlayers.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Five saponites with various substitution degrees of the constituent OH by fluorine were subjected to complex formation with α-naphthylamine to examine the effect of substitution on the stabilities of the resulting complexes. Saponite with a larger substitution degree intercalated a lesser quantity of a-naphthylamine and was broken down more easily in the reaction process. The complexes were subsequently heated in nitrogen to examine their thermostabilities. The thermostability of saponite was enhanced with increasing degree of substitution. All saponite, especially those without substitution, enhanced their thermostabilities by intercalating with α-naphthylamine. The reasons for these phenomena are briefly discussed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 25 (1990), S. 4847-4851 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Powders of saponite/acriflavine complex (SAC) saponite/carbon black mixture (SKM) and saponite itself (Sap) were pressed into small discs (20 mm diameter × 3 mm), followed by heat treatment at 1073 to 1473 K under nitrogen or argon. Their chemical resistance to 10% NaOH, conc. HCl, conc. HNO3 and conc. H2SO4 solutions at room temperature was examined on the basis of weight loss. The resistance of the three samples to NaOH solution was found to increase with increasing heat-treatment temperature, and both SAC and Sap after heating to 1473 K exhibited only a slight weight loss even after soaking for 20 d. On the whole, SAC had the highest resistance among three. The three samples were more resistant to acid solutions than NaOH, the resistance of both SKM and Sap increasing with increasing heat-treatment temperature. The amorphous component and forsterite crystal in the samples after heating to high temperature were preferentially attacked by NaOH and acid solutions, respectively. These results are discussed on the basis of X-ray diffraction, SEM observation, carbon content, etc.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 9 (1990), S. 693-695 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 16 (1981), S. 263-265 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 20 (1985), S. 255-260 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A thin film of montmorillonite-α-naphthylamine complex (MNC) was prepared, and then subjected to γ-ray radiation and heating to 473 K for polymerization of the inserted naphthylamine. MNC was subsequently heated to various temperatures below 1473 K under nitrogen. Montmorillonite film (Mont) was also treated in the same way as the reference sample. Compared with Mont, the MNC-layered structure was remarkably thermally stable and remained so slightly, even after heating to 1273 K. MNC was found to have a homogeneous porous structure after heating to 1273 K. Through comparison with Mont, the thermal degradation behaviour of MNC is discussed on the basis of X-ray diffraction, FT-IR, TG-DTA, elemental analysis, mass spectrum and SEM observations.
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