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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physica C: Superconductivity and its applications 190 (1991), S. 53-56 
    ISSN: 0921-4534
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Progress in Crystal Growth and Characterization of Materials 23 (1992), S. 341-367 
    ISSN: 0960-8974
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geosciences , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Ionics 51 (1992), S. 101-107 
    ISSN: 0167-2738
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Ionics 47 (1991), S. 271-275 
    ISSN: 0167-2738
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 44 (1997), S. 271-274 
    ISSN: 1572-879X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The catalytic activities of Fe-MFI (88% exchange) and Cu-MFI (122% exchange) zeolite catalysts for the decomposition and mainly the selective reduction of nitrous oxide by propene have been studied in the temperature range from 523 to 773 K. In the presence of oxygen and water vapor, both materials reveal strong retardation of their activity. When propene is added as reductant, Fe-MFI showed very high activity even in the low-temperature region and at low propene concentrations, whereas Cu-MFI is strongly deactivated.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Tetrahedron Letters 20 (1979), S. 1781-1782 
    ISSN: 0040-4039
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 27 (1992), S. 1499-1504 
    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 Polycrystalline alumina fibre was successfully synthesized by pyrolysis of a preceramic fibre formed from aluminium compounds with alkoxy and chelate ligands. A mixture of ethyl 3-oxobutanoatodiisopropoxyaluminium (EOPA) and tri-sec-butoxyaluminium (SBA) was reacted with glacial acetic acid yielding a polymeric product. The IR absorptions at 630 and 700 cm−1 due to the Al-O bond changed from sharp to broad bands by treatment with acetic acid. The 27Al resonance at 35 p.p.m. increased in intensity when EOPA-SBA (7/3) was treated with 30 mol% acetic acid. An increase in the EOPA to SBA ratio 5/5 to 9/1 also raised the intensity of the signal at 35 p.p.m. The viscosity of the polymeric product increased in intensity as the amount of acetic acid increased. The viscosity of precursor increased with increasing the ratio of EOPA to SBA, and decreased with increasing measurement temperature from 45 to 75°C. The precursor polymer pyrolysed at 500°C in air was amorphous to X-rays, and crystallized in γ-alumina at 840°C. The precursor fibres were pyrolysed to yield finegrained fibres of α-alumina at 1200°C for 1 h.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 26 (1991), S. 5292-5296 
    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 Polycrystalline alumina fibre was successfully synthesized by pyrolysis of preceramic fibre formed from aluminium chelate compound. Ethyl 3-oxobutanoatodiisopropoxyaluminium (EOPA) was reacted with glacial acetic acid yielding a polymeric product. The absorption bands ascribed to Al-O from 630–705 cm−1 changed from a sharp to a broad band on treatment with acetic acid. The13CNMR spectrum of EOPA changed from sharp singlets to multiplets after the reaction with acetic acid. The viscosity of the polymeric product increased in intensity with increasing amount of acetic acid. The viscosity of the polymeric product formed from EOPA-30 mol % acetic acid was 450 Pa s at 30 °C, and decreased to 5.4 Pa s with increasing measurement temperature from 30–70 °C. The27Al resonance at 35 p.p.m. increased in intensity with increasing viscosity of the polymeric precursor. The molecular weight of the precursor was distributed from 400–800. The polymeric precursor pyrolysed at 500 °C in air was amorphous to X-rays, and crystallized in γ-alumina at 840 °C. The precursor fibres were pyrolysed, to yield fine-grained fibres of α-alumina, at 1300 °C for 1 h.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 28 (1993), S. 105-110 
    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 Polycrystalline alumina-zirconia fibres were successfully synthesized by pyrolysis of preceramic fibres formed from mixed aluminium-zirconium chelate compounds. Ethyl 3-oxobutanoatodiisopropoxyaluminium (EOPA) was reacted with zirconium tetrabutoxide (TBZ) in the presence of glacial acetic acid yielding a polymeric product. The infrared absorptions from 500–625 cm−1 due to Al-O and Zr-O bonds changed from sharp to coalesced bands by treatment with acetic acid. The signal at 40 p.p.m. in the 27Al spectra of EOPA-TBZ increased in intensity on treating with acetic acid. The viscosity of the polymeric product increased as the amount of acetic acid increased. The viscosity of the precursor decreased on increasing the measurement temperature from 60 °C to 75 °C. The precursor polymer pyrolysed at 800 °C in air showed a broad X-ray diffraction of γ-alumina, and crystallized in a mixture of γ-alumina and tetragonal zirconia at 1000 °C. The median diameter of tetragonal zirconia in the α-alumina matrix was 33 nm, when EOPA-TBZ (Al/Zr=9/1) was heat treated at 1300 °C for 1 h. The precursor fibres were pyrolysed at 1300 °C to yield fine-grained fibres of α-alumina including tetragonal zirconia, which was confirmed by Raman microprobe spectroscopy.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 26 (1991), S. 3758-3762 
    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 Cubic BN was synthesized under high temperature and pressure conditions from BN powder formed by reaction of triammoniadecaborane (TAD) with ammonia. The BN powder formed from TAD and ammonia had a low degree of ordering. The crystal lattice of the BN powder increased in regularity with increasing synthesis temperature and time for the reaction of TAD with ammonia. The conversion yield of cubic BN at 1300 °C and 6.5 GPa in the presence of AIN increased with decreasing of reaction temperature of TAD and ammonia from 1000–700 °C. Cubic BN decreased in yield with increasing reaction time of TAD and ammonia at 800 °C. BN powder pre-heat treated at 1550 °C had a crystallite size,L c, of 22 nm, and was converted to cubic BN in a 43% yield at 1300 °C and 6.5 GPa for 10 min. The activation energy for cubic BN synthesis from BN powder-20 mol% AIN was 97 kJ mol−1, when the starting BN was synthesized at 800 °C. The conversion yield of cubic BN from the disordered BN-20 mol% AIN was 100% after heat treatment at 1300 °C and 6.5 GPa for 20 min.
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