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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 4181-4190 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Vinyl anthraquinone has been polymerized, via radiation-induced initiation, in dimethyl-sulphoxide and in dichloromethane. Solvent to monomer ratios of 1 : 0.030 to 1 : 0.0167 mol have been examined for dose rates in the range 0.035 to 0.129 Gy s-1 and exposure times in the range 1.44 × 104 to 4.32 × 106 s. Rates of polymerization were found to lie in the range from 2.4 × 10-8 to 1.92 × 10-6 mol L-1 s-1. Values for the chain transfer constant to dimethyl-sulphoxide and to dichloromethane have been calculated. In addition, values of the kinetic ratio kp2/kt, for the polymerization of 2-vinyl anthraquinone have been estimated. The dependence of Rp on the monomer concentration and on the radiation intensity have been shown to be in broad agreement with a simplified steady-state kinetic scheme. A value of G(radical) for 2-vinyl anthraquinone was obtained via electron spin resonance studies, and shown to be 0.24. This G(radical) value and those obtained indirectly from kinetic data are discussed in relation to the molar mass values obtained from the poly(2-vinyl anthraquinone) products.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3165-3178 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Vinyl anthraquinone was synthesized as described previously. In this article, three approaches to polymerization of 2-vinyl anthraquinone are examined bulk thermal, chemical, and γ-radiation-induced. Polymerization in both the bulk phase and in solution were attempted. Thermal characterization has been carried out using differential scanning calorimetry (DSC), x-ray diffraction (XRD), scanning electron microscopy (SEM) and hot-stage optical microscopy (HSOM). Thermogravimetric analysis (TGA) has been used to provide procedural “apparent” activation energies for decomposition of the polymer.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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