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  • 1985-1989  (7)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 2581-2586 
    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: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 1933-1934 
    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: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 739-745 
    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: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2469-2475 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is proposed for examining differences in the predictive capabilities of three versions of the free-volume theory of polymer - solvent diffusion using only a small amount of diffusivity data. The utility of the method is illustrated using a limited diffusivity data set for the methanol-poly(vinyl acetate) system.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 289-304 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The predictive and correlative capabilities of two recent versions of the free-volume theory for self-diffusion in polymer-solvent systems are examined by comparisons with experimental data. Neither the Vrentas-Duda free-volume theory nor the Paul version generally provides satisfactory predictions for the temperature and concentration variations of solvent self-diffusion coefficients. However, the Vrentas-Duda theory does provide good correlations of solvent self-diffusion data, and, furthermore, this theory can provide good predictions if a small amount of solvent self-diffusion data is used to help estimate the parameters of the theory. New diffusivity and equilibrium data were collected for the toluene-PVAc system to provide a broader database for evaluation of the self-diffusion theories.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 18 (1987), S. 265-272 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Procedures for the quantitative treatment of Raman spectra are proposed for the investigation of gallium-chlorine gaseous mixtures. They are based on correlations between pressures and Raman band intensities and require a knowledge of reliable entropy and heat capacity data for the main gaseous species. For the ratio Cl/Ga=3 and between 590 and 690 K, the pressure determinations from the band intensity evolution corresponding to the symmetric vibrational modes ‘ν1’ of Ga2Cl6 and GaCl3 confirm the starting consideration of the single equilibrium Ga2Cl6(g)⇌2GaCl3(g). They lead to an enthalpy of dissociation of Ga2Cl6 very close to the literature data. For Cl/Ga3 and between 800 and 950 K, the treatment of the Raman spectra is performed by computation of the GaCl spectrum in order to discriminate between the GaCl3 ‘ν1’ band intensity and the GaCl ‘νs’ branch intensity. This intensity difference and the GaCl ‘νQ’ branch intensity are used for pressure determinations. The results are consistent with the proposed equilibrium 2Ga(l)+GaCl3(g)⇌3GaCl(g). They lead to a calculated reaction enthalpy that allow one to select a reliable value for the enthalpy of formation of GaCl.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular vibration frequencies of the gallium-chlorine gaseous species were selected. For the known species Ga2Cl6, GaCl3 and GaCl selection was performed by comparing previous experimental values with our own Raman spectrometric determinations. For the unidentified species Ga2Cl4, Ga2Cl2 and GaCl2 frequency values were evaluated from theoretical literature considerations. The Raman spectra of the vapours obtained by heating condensed gallium and chlorine mixtures are discussed using the selected frequencies and taking into account the Ga2Cl6 and GaCl3 detection limits. With our Raman recording conditions corresponding to well defined spectra, the species are detected up to 5 × 10-3 at. Under these conditions, for Cl/Ga = 3 and between 70 and 500 °C, the main gaseous species are GaCl3 and Ga2Cl6 and the system should be described by the single equilibrium: Ga2Cl6(g)⇌2GaCl3(g). For Cl/Ga = 0.122-3, and between 300 and 800 °C, the representation of the system should be simplified to a single heterogeneous equilibrium between the major species: 2Ga(I)+GaCl3(g)⇌3GaCl(g). In this case, the evolution of the Raman spectra with temperature is explained by taking into account contribution of Ga2Cl4 in very small amounts.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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