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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.
    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
    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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  • 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
    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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  • 6
    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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  • 7
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Infection of BHK cells with western equine encephalitis (WEE) virus resulted in rapid inhibition of cellular DNA synthesis. The rate of inhibition of DNA synthesis depended on the multiplicity of infection, and was closely related to virus replication. Cellular DNA synthesis was not inhibited in infected BHK cells that had been irradiated with ultraviolet radiation. These results indicated that a functional viral genome was required for the inhibition of DNA synthesis by WEE virus. The sharp decrease in thymidine incorporation into the acid-insoluble fraction was not due to a change in the intracellular pool of the acid-soluble fraction. Sedimentation analysis in alkaline sucrose gradients was used to show that cellular DNA was not degraded during WEE virus infection. DNA polymerase activity in infected cells was not significantly reduced.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The characteristics of an avian influenza virus were compared in detail with those of human Asian (H2N2) influenza viruses. Antigenic analysis by different antisera against H2N2 viruses and monoclonal antibodies to both the hemagglutinin and neuraminidase antigens showed that an avian isolate, A/duck/München/9/79 contained hemagglutinin and neuraminidase subunits closely related to those of the early human H2N2 viruses which had been prevalent in 1957. However, this avian virus gave low HI titers with absorbed and non-absorbed antisera to different human H2N2 viruses isolated in 1957. Like human Q phase variant, such as A/RI/5−/57 (H2N2), hemagglutination of the above avian strain was not inhibited by the purified non-specific γ-inhibitor from guinea pig serum. Growth behavior at restrictive temperature (42° C) clearly differentiate the avian H2N2 virus from human influenza viruses, showing that the former virus grew well in MDCK cells at 42° C but not the latters. Genomic analysis of these viruses revealed that the oligonucleotide map of H2N2 virus isolated from a duck was quite different from those of human H2N2 viruses from 1957 to 1967. The oligonucleotide mapping also indicated that different H2N2 influenza virus variants had co-circulated in humans in 1957.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Specific antisera for the isolated HN proteins of eight reference strains of avian paramyxoviruses could be prepared in guinea pigs by intraperitoneal injection of guinea pig red blood cells (GRBC) coated with purified HN proteins. In the hemagglutination inhibition (HI) tests, all reference strains reacted strongly with each homologous antiserum to the isolated HN showing that a low level of cross-reactivity among the reference strains was greatly diminished by using specific antisera. Immuno-double-diffusion (IDD) tests showed that all antisera except those to turkey/Wisconsin/68 and duck/Hong Kong/D3/75 gave single well-defined lines only with the homologous viruses. The remaining two antisera developed a single definite precipitin line together with weak lines with homologous virus. Two isolates in Japan were clearly identified in HI and IDD tests with specific antisera to the HN subunits of the reference strains suggesting that the antisera were useful for identification of avian paramyxovirus isolates. Two isolates in Japan, H-70 from a munia-bird and Y-7 from a duck were found to have HN proteins related closely to those of finch/N. Ireland/Bangor/73 and duck/Hong Kong/199/77, respectively.
    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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