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  • 1
    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
    Type of Medium: Electronic Resource
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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
    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.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0264-410X
    Keywords: Cholera toxin ; E. coli heat-labile toxin B subunit ; adjuvant ; cholera toxin B subunit ; influenza ; nasal vaccine
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0264-410X
    Keywords: E. coli enterotoxin B subunit ; Influenza vaccine ; adjuvant
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    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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  • 7
    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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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 20 (1985), S. 516-523 
    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 heated to various temperatures below 1473 K for 5 min under nitrogen. The resulting samples were further heated to 1073 to 1473 K for 30 min or 5 h in air to examine their oxidation resistivities. A thin montmorillonite film was also treated in the same manner for reference purposes. The layered structure of MNC was retained up to 1273 K under nitrogen, although it changed gradually to an amorphous state with increase in temperature. MNCs after heating below 1073 K under nitrogen were changed to montmorillonite by subsequent heating to 1073 K for 30 min in air, whereas, MNCs heated to 1173 and 1273 K under nitrogen retained somewhat their layered structures, even after heating to 1173 K for 30 min in air. The causes for such differences are discussed on the basis of the results obtained from X-ray diffraction, thermogravimetry, FT-IR and SEM observation.
    Type of Medium: Electronic Resource
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  • 9
    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.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The hemagglutinin-neuraminidase (HN) subunits of NDV and NDV-like isolates were analyzed antigenically by monoclonal antibodies to the HN of Miyadera and Taka viruses. In immuno-double-diffusion (IDD) tests, all NDVs examined gave clear lines of precipitation with some of the potent monoclonal antibodies, but it was difficult to determine with certainty the immunological properties of HN subunits due to a rare disagreement with the results obtained in other immunological tests. Monoclonal antibodies used in the tests were found to show different immunological reactivities with the viruses. Monoclonal antibodies belonging to the 1st group (1/29) inhibited the hemagglutinating (HA) activity of all strains but not the neuraminidase (NA) activity. The second monoclonal antibody (5/205) inhibited both the HA and NA activities of the restrictive NDV strains, indicating antigenic changes in HN molecules. However, the inhibitory activity of this monoclone to neuraminidase appeared to be greatly diminished when neuraminyl lactose was used as substrate. Although the 3rd type of monoclonal antibody (5/220) showed HI activity against several strains, this antibody did not inhibit NA activity of any viruses. The remaining monoclone to the HN of Taka virus inhibited the HA activity of all reference strains of NDV and many NDV-like isolates but did not affect NA activity. Two inhibitory activities of four monoclonal antibodies against different viruses, HI and hemolysis-inhibition, were not always consistent with inhibition of virus growth. HI and NI tests with the above four monoclonal antibodies showed that the strains tested fell into five antigenic groups according to their reaction patterns with mouse hybridoma antibodies.
    Type of Medium: Electronic Resource
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