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  • Polymer and Materials Science  (6)
  • Analytical Chemistry and Spectroscopy  (2)
  • COMPOSITE MATERIALS
  • 1985-1989
  • 1980-1984
  • 1970-1974  (8)
  • 1970  (8)
Collection
Keywords
Publisher
Years
  • 1985-1989
  • 1980-1984
  • 1970-1974  (8)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 277-287 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies have been made on the dynamic and steady-shear melt rheology of an ethylene-methacrylic acid copolymer and two of its salts obtained by partial neutralization with sodium and with calcium bases. Measurements were made with a Weissenberg rheogoniometer over a broad range of shear rates and frequency in the temperature interval mainly from 100 to 160°C. The temperature coefficients of dynamic and steady shear viscosity are evaluated at both constant shear rate and constant stress. Likewise, complex dynamic viscosities and apparent high steady-flow viscosities and intercompared at equivalent frequencies and shear rates. The un-ionized acid copolymer shows good correlation between the frequency dependence of the complex viscosity and the shear rate dependence of the apparent viscosity. This is not true for either the sodium salt or the calcium salt. These results are consistent with the two-phase structural model for these materials, i.e., a matrix of hydrocarbon in which are embedded ionic domains.
    Additional Material: 12 Ill.
    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 14 (1970), S. 2697-2706 
    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: A survey of viscoelastic data on amorphous polymer melts indicates that the steady-state shear compliance, Je, of many systems can be approximated from a knowledge of their flow response. For systems with monomodel molecular weight distributions, the absolute value of the reduced complex viscosity, η*/η0, is found to equal 0.67 ± 0.03 at the frequency ω, where ωη0Je = 1. This result applies to a variety of polymer systems and to a wide range of molecular weights and distributions as long as the highest molecular weight dispersion of the distribution constitutes more than 20 weight per cent of the sample. This relationship determines Je from non-Newtonian flow data and thus provides a consistent way to relate differently shaped reduced variable curves and to calculate compliances from characteristic times reported in the literature. The connection between some commonly used times and Je is given. The method of calculating Je is successfully applied to capillary measurements of melt viscosities and to characteristic times determined from steady-state shear measurements of concentrated polymer solutions.
    Additional Material: 6 Ill.
    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 14 (1970), S. 879-896 
    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: An investigation was made of the magnitude and mechanism of shear degradation of a narrow distribution, high molecular weight (Mw = 670,000) polystyrene. An Instron rheometer was used to perform the extrusion at temperatures from 164° to 250°C. The change in molecular weight distribution was studied by gel permeation chromatography. The maximum shear stress employed was 5.83 kg/cm2. It was found that degradation could be induced at high stress at temperatures of 50°C lower than degradation of polystyrene would occur exclusively due to thermal forces. An activation energy for the degradation, calculated at constant shear rate, was +20.2 kcal/mole. The direction and magnitude of this value are consistent with degradation induced through a mechanical reduced activation for thermal degradation.
    Additional Material: 15 Ill.
    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 14 (1970), S. 2305-2317 
    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: High-density commercial polyethylenes have been crystallized under the combined orientation and pressure effects available in the Instron capillary rheometer. The samples so formed were found to have a high degree of crystal perfection and crystal orientation in combination with the unusual property of transmitting visible light. The procedure for forming the crystal structure is elucidated. X-Ray and differential scanning calorimetry techniques were utilized to initiate a study of the structure. Evidence is presented that is consistent with the presence of an extended chain component in the crystal structure.
    Additional Material: 6 Ill.
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  • 5
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The m/e 226 peak in the mass spectrum of 1,1-dimethyl-2,2-dibenzoylhydrazine is formed by loss of C2H4N from the molecular ion, a process involving concerted transfer of two hydrogen atoms from the same methyl group as an accompaniment to N—N bond fission.
    Additional Material: 1 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 1259-1282 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of C-alkylaziridines show that generally β-cleavage is the most important fragmentation, although α-cleavages also occur as do γ-, and δ- and ∊-cleavages in appropriate examples. A surprising rearrangement of the β-cleavage ions has been explained as the result of a four-centre cyclization followed by fragmentation. Other decompositions occur via transannular cleavages with and without hydrogen transfer. α-Cleavage appears to be the most important fragmentation of N-alkylaziridines. N-Phenylaziridine shows very marked 1,2-phenyl-migration before fragmentation.
    Additional Material: 13 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 8 (1970), S. 177-181 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 8 (1970), S. 671-675 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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