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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 264-268 (Feb. 1998), p. 1129-1132 
    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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  • 2
    ISSN: 1090-6509
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The magnetic properties of the intermetallic compounds Gd1−x YxMn2Ge2 (0≤x≤0.5) (tetragonal crystal structure of the type ThCr2Ge2) have been measured in fields up to 40 T in the temperature range 4.2–120 K on free powders (whose particles are free to rotate in a magnetic field), fixed powders, and polycrystalline bulk samples. The temperature dependence of the crystal structure parameters of some of these intermetallic compounds was determined from x-ray diffraction measurements. It was found that the temperatures of magnetic disordering of the gadolinium magnetic subsystem and the transition of the manganese subsystem from the ferromagnetic to the antiferromagnetic state decrease as the gadolinium content is decreased, so that in compositions with x〈0.3 this transition is a first-order phase transition, and with further decrease of the gadolinium content it becomes second-order. In intermetallic compounds of this system with x=0.3 and 0.4 another spontaneous first-order transition is observed at lower temperatures. In a magnetic field the magnetization of all the investigated intermetallic compounds except for the composition x=0.5 undergo a metamagnetic transition. The T-x, H-x, and H-T magnetic phase diagrams are constructed. The experimental data are interpreted with allowance for the fact that according to the results of previous studies, the Mn-Mn exchange interaction is antiferromagnetic, and thus the examined intermetallic compounds are two-sublattice ferrimagnets with negative exchange interaction in one of the sublattices. Calculations performed within the framework of this model in the Yafet-Kittel approximation, which assumes that the sublattice with negative exchange can be divided into two sub-sublattices, permit a quantitative description of the experimental results in most cases.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 71 (1997), S. 122-124 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Strain effects on critical current densities have been examined for conductors containing nearly stoichiometric Nb3Al filaments with fine grains. The Nb3Al phase in these multifilamentary conductors are prepared by phase transformation from supersaturated Nb(Al) bcc solid solution and show high-field critical current densities much larger than those for conventionally prepared Nb3Al conductors, where the Nb3Al phase is known to be off-stoichiometric. The degradation of critical current densities with −0.7% intrinsic strain is ca. 20% at 12 T, comparable with those for conventional Nb3Al conductors of high strain tolerance. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 69 (1996), S. 677-678 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We have found the effects of HgTe layers on dislocations of (111)B HgCdTe layers grown on Si substrates by metalorganic vapor phase epitaxy. The dislocations in HgCdTe layers were reduced by inserting thin HgTe layers between HgCdTe and CdTe buffer layers. Using this method, the dislocation density of 2.3×106 cm−2 was obtained, which is less than quarter that of HgCdTe layers without HgTe. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 69 (1996), S. 2876-2878 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: CdTe(1¯ 1¯ 3¯)B epilayers were grown on Si substrates oriented (112)5° off toward the [1¯ 1¯ 1] direction by molecular beam epitaxy (MBE). A Zn irradiation process was developed in order to obtain a (1¯ 1¯ 3¯)B face. HgCdTe(1¯ 1¯ 3¯)B epilayers were grown on 20 μm-thick CdTe/Si(112) 5° off, and characterized. These layers have double-crystal x-ray rocking curves with full width at half-maximum as low as 64 arc s, and etch pit densities of 4.4×106 cm−2 and 2.6×105 cm−2 for as-grown and thermal-cycle annealed films, respectively. Photodiodes were also fabricated to demonstrate the capability of large-area MBE-HgCdTe/Si focal-plane arrays. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 8 (1997), S. 431-435 
    ISSN: 1573-4846
    Keywords: lithium borate ; addition of acid ; suppressor mechanism of crystallization ; boron-containing species ; residual carbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Lithium borate films in amorphous and crystalline(Li2B4O7)states were prepared from alkoxide solutions hydrolyzed in thepresence or absence of hydrochloric acid or acetic acid. The acidssuppressed crystallization of the amorphous films intoLi2B4O7, with acetic acid being the stronger suppressor. Inorder to determine the suppressing mechanism, we investigated thedistribution of boron-containing species in the solutions by 11B-NMR. Boron in the non-acidified solution existed as bothB(OH) $$_4^ - $$ and polyborate species, includingB4O5(OH) $$_4^{2 - } $$ , which is easilytransformed into the crystalnucleous of Li2B4O7. In the solutionscontaininghydrochloric acid or acetic acid, however, boron was present mainlyas B(OH)3 and the formation of the polyborate species wassuppressed, leading in turn to the suppression of crystallizationinto Li2B4O7. X-ray fluorescence analysis showed thatacetic acid produced a larger amount of residual carbon in the filmsthan did hydrochloric acid. We concluded that the residual carbonalso inhibited crystallization of the films intoLi2B4O7.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 8 (1997), S. 431-435 
    ISSN: 1573-4846
    Keywords: lithium borate ; addition of acid ; suppressor mechanism of crystallization ; boron-containing species ; residual carbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Lithium borate films in amorphous and crystalline (Li2B4O7) states were prepared from alkoxide solutions hydrolyzed in the presence or absence of hydrochloric acid or acetic acid. The acids suppressed crystallization of the amorphous films into Li2B4O7, with acetic acid being the stronger suppressor. In order to determine the suppressing mechanism, we investigated the distribution of boron-containing species in the solutions by11B-NMR. Boron in the non-acidified solution existed as both B(OH) 4 − and polyborate species, including B4O5(OH) 4 2− , which is easily transformed into the crystal nucleous of Li2B4O7. In the solutions containing hydrochloric acid or acetic acid, however, boron was present mainly as B(OH)3 and the formation of the polyborate species was suppressed, leading in turn to the suppression of crystallization into Li2B4O7. X-ray fluorescence analysis showed that acetic acid produced a larger amount of residual carbon in the films than did hydrochloric acid. We concluded that the residual carbon also inhibited crystallization of the films into Li2B4O7.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 13 (1998), S. 223-227 
    ISSN: 1573-4846
    Keywords: lithium boracite ; lithium-ion conductor ; complex impedance method ; by-products ; morphology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The electrical properties of polycrystalline lithium chloroboracite, Li4B7O12Cl, prepared by the sol-gel method were investigated in connection with their structure. Li4B7O12Cl pellets were prepared with different amounts of hydrochloric acid or ammonium chloride. The kind and amount of the chlorine source affected the formation of by-products (Li2B4O7, LiCl, a glass phase) and the morphology of the Li4B7O12Cl pellets. Thus their conductivity, which is dominated by grain boundary response owing to the high porosity of the materials, was also affected. The formation of Li2B4O7 as a by-product led to a higher activation energy and lower conductivity. In those pellets in which Li2B4O7 did form, an increase of the amount of glass phase led to higher conductivities.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 150 (Feb. 1998), p. 121-128 
    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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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 31 (1996), S. 537-544 
    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 The reaction sequences in the synthesis of aluminium borate whiskers from the raw material mixtures (Al2(SO4)3/H3BO3/K2SO4, K2SO4 as a flux) were investigated by differential thermal analysis-thermogravimetric analysis (DTA-TG), X-ray diffraction analysis (XRD), and a direct observation of the reacting mixture. DTA of a mixture with the optimum composition for obtaining well-grown whiskerswith a high yield, and XRD of the same mixtures quenched at various temperatures, showed that the reaction proceeds through formation and decomposition of double salts of aluminium: first tripotassium aluminium sulphate and then monopotassium aluminium sulphate. This reaction sequence and the DTA results of mixtures with different K2SO4/(Al-B) ratios were successfully explained by the phase diagram of the Al2(SO4)3 K2SO4 system. Direct observation of the reacting mixture confirmed the explanation. The compositions of reacting mixtures were then calculated from the TG data and traced on the phase diagram. The tracing showed that the decomposition of aluminium salts occurred in different physical states, depending on the K2SO4/(Al+B) ratio, in solid, solid and then liquid, or liquid phase. This difference in decomposition explained well the effect of the K2SO4/(Al+B) ratio on the morphology of the whiskers. The effect of the B/Al ratio in the mixture was similarly explained by the correlated change in the K2SO4/Al ratio.
    Type of Medium: Electronic Resource
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