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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Economics Letters 35 (1991), S. 1-4 
    ISSN: 0165-1765
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Economics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Economics Letters 38 (1992), S. 399-403 
    ISSN: 0165-1765
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Economics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Polyhedron 5 (1986), S. 179-182 
    ISSN: 0277-5387
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Applied Surface Science 75 (1994), S. 213-219 
    ISSN: 0169-4332
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Ricerche Economiche 47 (1993), S. 363-383 
    ISSN: 0035-5054
    Keywords: Indivisibilities ; Nash implementation ; Walras equilibrium ; [JEL classification codes] O21 ; [JEL classification codes] O26
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Economics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 10 (1979), S. 207-211 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Ъыло найдено, что гндрат молибдата никеля является эффективным прекурзором в гидродесульфуризации тиофена. Прокаливание гидрата при 300°C и пресульфидирование с помощью H2S представляет собой обработку, благоприятствующую повышению активности.
    Notes: Abstract Nickel molybdate hydrate has been found to be an effective precursor catalyst for the hydrodesulfurization of thiophene. Calcination of the hydrate at 300°C and presulfidation with H2S are favorable treatments for higher activity.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-1858
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Technology
    Notes: Abstract  In the field of III–V-based compounds, new functionalities can be reached by integrating micromechanical structures with electro-optical functions, in order to fabricate Micro Opto Electro Mechanical Systems (MOEMS). A possible application is an InP-based integrated optical stress sensor. Such a system is based on a partly suspended waveguide that can be strained under the effect of an external stress. The photoelastic effect induces a phase shift that can be converted into an intensity shift of the signal if the device is configurated as a Mach-Zehnder interferometer. This system can be integrated monolithically with the optical source and the photodetector. The mechanical, photoelastic and optical properties of this structure has been simulated in order to configurate the alloy composition of the epitaxial layers and the geometry of the device. Micromachining processes have been developed in order to realize InP-based suspended microstructures by sacrificial layer etching and bulk micromachining. Preliminary results showed that the optical behaviour of the waveguides is close to the theoretical analysis. Characterisation of the complete interferometer is underway in our group.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-5225
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary Spruce wood (Picea abies) was disintegrated into extremely fine powder and the resulting particles were resolved according to their density by centrifugation into the following main fractions: M (middle lamella fraction) containing 49.1% lignin and S (secondary wall fraction) containing 23.1% lignin. These main fractions were further subjected to ball milling at -15°C and extraction (dioxane-water) after which the polysaccharides were hydrolyzed by enzymic treatment and lignin was extracted. Finally, the material representing the main fractions M and S was divided into two subfractions (soluble (s) and insoluble (i)) using 1,2-dichloroethane-ethanol (2:1) as solvent. The lignin in the subfractions (primarily the s fractions) was characterized by spectroscopic methods (1H NMR, 13C NMR, IR, and UV). Further information was obtained by methoxyl analyses and chromatography of the fragments obtained after methylation and permanganate and nitrobenzene oxidations of the main fractions. The molecular weight distribution of the isolated lignin was also determined (by GPC). Finally, the main fractions were hydrolyzed and the resulting monosaccharides were determined as alditol acetates by GLC. Because of uncertainties associated with the experimental techniques no strictly quantitative conclusions could be drawn from the results obtained and there were only few indications of structural differences in the lignins according to their morphological location. The rather small differences obtained allow the following tantative conclusions: Compared with secondary wall lignin, middle lamella lignin contained somewhat more open α-O-4 linkages as well as structures with β-β linkages but less structures containing β-O-4 linkages. No conclusive evidence was found for the differences in the content of either β-1 linkages or phenolic and aliphatic hydroxyl groups. However, somewhat fewer methoxyl groups and phenylcoumaran structures and more carbonyl groups (at least at α-position associated with free phenolic structures) were present in the middle lamella than in the secondary wall lignin and the data also indicated a slightly higher degree of condensation of the former lignin. Considerable differences were found in the carbohydrate composition: the middle lamella fraction contained more rhamnose, arabinose, and xylose moieties than the secondary wall fraction whereas the opposite was true for the content of mannose and glucose.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 28 (1994), S. 69-77 
    ISSN: 1572-879X
    Keywords: sulfided CoMo catalysts ; supported catalysts ; active carbon support ; vapor phase carbonylation ; methanol carbonylation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Methanol carbonylation has been carried out over carbon supported sulfided CoMo catalysts without addition of CH3I, as promoter, to the feed. A temperature around 250°C, and methanol concentrations higher than 5 mol% were found to be optimum for ester production. Sulfided Mo/C catalysts were inactive for methanol carbonylation, methane being the major product. While sulfided Co/C catalysts were as effective for ester production as CoMo/C catalysts, methanol conversion was higher in the latter. The selectivity to methyl acetate was found to be strongly dependent on the nature of the carbon support.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1572-879X
    Keywords: HDN ; carbon-supported catalysts ; NiMo catalysts ; sulfided catalysts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The hydrodenitrogenation (HDN) of pyridine over activated carbon-supported Mo and NiMo sulfided catalysts was studied. Without H2S in the feed the catalysts showed a high conversion of pyridine and of piperidine to C5 hydrocarbons at the beginning of reaction, followed by a strong deactivation. A large increase in the conversion of pyridine was observed when H2S was added to the feed at H2S/H2⩾0.006. The conversion of piperidine to C5 hydrocarbons was enhanced by H2S and it increased as the H2S pressure increases up to H2S/H2⩾0.006. The promotion effect of Ni was operative only when H2S was present and it increased with the H2S/H2 ratio. Without H2S, the degree of surface oxidation of the support affected the deactivation of the catalysts. When H2S was added to the feed, the conversion of pyridine was stable and independent of the acid treatment of the support. A more oxidized support enhanced the C-N bond breaking reaction.
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