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  • Physics  (8)
  • 1975-1979  (8)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 2595-2605 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decomposition of hydrogen peroxide by a polymer complex of Fe3+ and poly(acrylic acid) partially amidated by diethylenetriamine has been studied. The molecular mechanism of catalysis is discussed. The rate constant of the reaction is k = 6.9 × 107 exp {-2.300/RT}. Decomposition of hydrogen peroxide proceeds via activation by the diethylenetriamine which is a cofactor.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 2199-2215 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoinitiated homophase polymerization of methyl methacrylate (MMA) at 25°C in the presence of a complexing agent, orthophosphoric acid (H3PO4), was studied. It was found that in addition to the increase in initial polymerization rates and molecular weights of PMMA the system MMA/H3PO4 reveals postpolymerization that does not retard with time and is accompanied by an increase on average molecular weight. Macroradicals, lifetimes of which grow considerably in the presence of the complexing agent, are shown to be responsible for the termination-free postpolymerization in this system by the living chain mechanism. The effect of various factors on the kinetics of postillumination polymerization was studied. A drastic decrease in the rate of bimolecular termination of poly(methyl methacrylate) radicals was shown to be related to the change in conformational properties and to the association of propagation chains via complexing with H3PO4. The mechanism of polymerization in this system was discussed.
    Additional Material: 10 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 1777-1778 
    ISSN: 0360-6376
    Keywords: Physics ; 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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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 613-616 
    ISSN: 0360-6376
    Keywords: Physics ; 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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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1255-1266 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced grafting polymerization of phenylacetylene and 2-methyl-5-vinylpyridine (2M-5VPy) onto low-density polyethylene has been investigated under strict identical conditions, using crude and thoroughly dried monomers. In the case of thoroughly dried monomers, the radiation-induced grafting is performed by the combined (radical + anionic) mechanism. The kinetics of radical and anionic grafting of 2M-5VPy are investigated in detail. The activation energies are 4.8 ± 0.3 and -2.7 ± 0.3 kcal/mole for the radical and anionic grafting, respectively. The initial rate of grafting is approximately proportional to the dose rate to the 0.47 ± 0.03 and 0.92 ± 0.03 power for the radical and anionic grafting, respectively. The initial rate of grafting is approximately proportional to monomer concentration to the 1.55 ± 0.05 and 2.1 ± 0.05 power for the radical and anionic grafting, respectively. These data conform to the contribution of the anionic mechanism in a thoroughly dried system. The mechanism of radiation-induced anionic grafting is discussed.
    Additional Material: 10 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 1773-1775 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 2351-2356 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zwitterionic matrix stepwise polymerization of 4-vinylpyridine (VP) using isotactic poly(acrylic acid) (i-PAA) as a template results in formation of crystalline polycomplexes consisting of i-PAA and of ionene (I): Depending on the concentration of VP and i-PAA, the two types of crystalline polycomplexes can be prepared. The complex containing long ionene sequences with n ≫ 2 is formed when [VP]0 = [i-PAA]0 ≥ 0.05M. At [VP]0 = [i-PAA]0 ≤ 0.01M, the complex formed evidently contains the ionene dimer (n = 2). The x-ray structures of the crystalline complexes are identical with those obtained by mixing of i-PAA and the corresponding dimer and polymer presynthesized in the absence of the template. The matrix polymerization of VP in the presence of syndiotactic and atactic PAA at the same conditions results in formation of amorphous polycomplexes.
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 1825-1828 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced grafting of acrylonitrile, 4-vinylpyridine, and styrene was carried out by both radical and ionic mechanisms. Grafted polymers with equal percentages of graft were obtained by the radical and ionic propagation of the grafted chains. The molecular weight of homopolymers has been determined. The thermomechanical properties of the graft polymers were investigated. The yield temperatures for the graft polymers obtained by ionic propagation of the grafted chains is higher than that of graft polymers obtained by a radical mechanism. This is attributed to the higher molecular weight of the grafted chains obtained by the radiation-induced grafting by the ionic mechanism. The radiation-induced grafting of polyacrylonitrile increases significantly the thermal stability of polyethylene. The differential thermal analysis shows no marked differences in properties of the polymers.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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