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  • Chemistry  (29)
  • Lunar and Planetary Science and Exploration  (12)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemical Engineering & Technology - CET 12 (1989), S. 262-269 
    ISSN: 0930-7516
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Studies of flow characteristics and residence time distribution, (RTD), have been undertaken in a range of geometrically similar, laboratory nozzle-type reactors. High-speed cine-photography was employed to record the complex phenomena of liquid mixing in the reactor and also to record on film the colour of an injected tracer solution leaving in the effluent. A novel atomic absorption spectrophotometric (AAS) technique was applied to transform the results of the latter film into response curves. This technique provide detailed quantitative data on the residence time distributions (RTD) for different feed rates. A multiparameter model, comprising a network of CSTR's and plug flows, was developed to simulate the experimental response data. Good agreement was obtained between model predictions and experimental results. The experimental technique and theoretical approach are recommended for analyzing the flow patterns and mixing mechanisms in such reactors.
    Additional Material: 13 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemical Engineering & Technology - CET 15 (1992), S. 186-192 
    ISSN: 0930-7516
    Keywords: Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A study was made of mass trasfer rates from single large oscillating drops of pure liquid-liquid systems, in the size range of 5 to 10 mm. A thrermostatically-controlled, 50 mm in diameter, 1000 mm long, rising drop column was used, in which mirrors in the jacket enabled front and side views of drops to be photographed simultaneously. The systems studied were (1) toluene and acetone (dispersed)-water (continuous), and (2) n-heptane and acetone (dispersed)-water (continuous). High concentrations of acetone (up to 3.75 kmol/m3) were used to examine the effect of different parameters on the mass transfer rate, frequency and amplitude of oscillation in countercurrent operation. Previous theories and empirical correlations [2-6, 12, 13, 15] for the prediction of overall mass transfer coefficients showed large deviations from measured values. These may have aarisen because the models do not represent droplet oscillation accurately, and/or apply only to oscillations of small droplets. Fair agreement was obtained for small oscillating droplets as low solute concentrations. The oscillations of a travelling drop were asymmetrical; the period of oscillation was uniform for mutually-saturated systems but changed when mass transfer was taking place. The periods were longer than those predicted by the Lamb [7] and Shroeder and Kintner [37] correlations. Terminal velocities predicted from literature correlations [32, 34] did not give reasonable agreement with experimental data when there was mass transfer of solute. The drag coefficient increased with increasing mass transfer rate from the drop. Correlation of the results and the dispersed phase mass trasfer coefficients by dimensional analysis resulted in the correlation List of symbols at the end of the paper. \documentclass{article}\pagestyle{empty}\begin{document}$$ k_d = 1.6 \times 10^6 \varepsilon ^{2.82} Eo^{1.15} Sc^{ - 2.0} \sqrt {D_d \omega _{\exp } } $$\end{document} with a mean deviation of ±23%, by insertion of experimental oscillation frequency data. This will facilitate more accurate prediction of the dispersed phase mass transfer coefficients relating to equipment containing droplets in the oscillating regime, e.g. pulsed columns or agitated tanks.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 254-254 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 255-256 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 329-335 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Molecular weight distributions of homopolymer and graft polymer obtained from the gamma and photoinitiated polymerization of methyl methacrylate with natural rubber latex have been determined. Broad distributions were found with peaks of low and high molecular weight polymer. The distributions were insufficiently defined to make definite assignments to the speeds of the reactions involved but were not inconsistent with the mechanism proposed in an earlier paper from kinetic considerations. Details are given of the column fractionation apparatus employed.
    Additional Material: 7 Ill.
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  • 6
    ISSN: 1040-0397
    Keywords: Hydrogen peroxide ; Palladium ; Thin-film ; Electrocatalysis ; Sensors ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A thin-film composite metal electrode is described for the amperometric measurement of hydrogen peroxide. By thermally evaporating a 27 μM layer of gold/palladium through a copper mask onto a plastic substrate a number of chemically equivalent sensing elements can be prepared. On these electrodes, hydrogen peroxide can be oxidized at a voltage of 0.4V (SCE). A model for the oxidation of peroxide at these electrodes is described based upon reversible binding of hydrogen peroxide to electrochemically generated palladium oxide sites.
    Additional Material: 10 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 445-445 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 417-427 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The use of ultrafein filters as osmotic membranes has been investigated in various solvents. It has been found that, at 30°C., measurements can be made in benzene, toluene, ethanol, water, and, with difficulty, methyl ethyl ketone, but not in chloroform or dimethylformamide. In benzene it has been found that all grades of the membranes are more selective than the corresponding ultracella filters and that, with the allerfeinst grade, molecular weights of the order of 2000 can be determined. With solutions of pentaerythritol tetrastearate (M.W. 1200), tristearin (M.W. 891), and sucrose octaacetate (M.W. 679), the osmotic pressures developed were less than the theoretical values. The ratios of observed to theoretical osmotic pressure decreased with molecular weight, and these ratios appear to be examples of the reflection coefficients predicted by Staverman.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 37 (1959), S. 241-250 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Gamma- radiation induced graft copolymerization of methyl methacrylate with natural rubber is characterized by high yields of grafted polymer even at relatively high monomer concentrations. The rates are first order except at low monomer concentrations; above 95% rubber concentration the polymerization rates are very low. A reaction mechanism has heen proposed in which it is shown that these results are consistent with a relatively slow initiation step between rubber radicals and methyl methacrylate and a rapid crossed termination reaction between methacrylate radicals and rubber radicals. In order to explain the high yield of grafted polymer, it has been assumed that radicals produced from methyl methacrylate by gamma-radiation are, unlike the growing methacrylate chains, capable of attacking the rubber molecule and thus from sites for grafting to occur, and also that monomer transfer is negligeable.
    Additional Material: 4 Ill.
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  • 10
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Linear polybutadienes, prepared with butyllithium as catalyst, and polybutadienes branched by exposure to γ-radiation have been fractionated and the fractions examined by osmometry and light scattering. Turbidimetric second virial coefficients (A2τ) of mixed polymer fractions are virtually the same as those of the higher molecular weight components of the mixtures for most compositions. This is true both for mixtures of linear with linear and linear with branched polymer. The higher the molecular weight of the fraction, the greater the effect; the addition of 1% microgel to a linear polymer reduced A2τ by a factor of three. The presence of microgel or high molecular weight branched polymer has been shown to be responsible for the very high molecular weights previously reported for polybutadienes from light scattering measurements. It is conveniently removed by shaking the solutions with calcium sulfate. Second virial coefficients obtained either by light scattering or osmometry are, within the limits of experimental error, uninfluenced by branching in the polymer. In general those factors which lead to increased branching also result in increased polydispersity, and it is the latter which results in the decrease in A2τ. The fall of the osmotic second virial coefficient (A2τ) with molecular weight is much smaller than would be calculated theoretically, and the fall in A2τ is greater than would be expected, notwithstanding the fact that for some of the fractions M̄u/M̄n 〈 1.1. This indicates that A2π is sensitive to the low molecular weight species presented in the fractions, whereas the reverse must apply to A2τ. Natural of synthetic trans-polyisoprene showed analogous behavior to polybutadiene, although, owing to experimental difficulties, sharp branched fractions could not be obtained. The following viscosity-molecular weight relationships were obtained in benzene solution: [η] = 1.45 × 10-4M0.76 for butyllithium-catalyzed polybutadienes, and [η] = 4.37 × 10-4M0.65 for natural and synthetic trans-polyisoprenes.
    Additional Material: 12 Ill.
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