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  • 2020-2024
  • 1960-1964  (5)
  • 1935-1939
  • Polymer and Materials Science  (5)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 62 (1962), S. 73-82 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal oxidative degradation of an inhibited butadiene-acrylonitrile copolymer has been studied kinetically by means of infrared spectroscopy and color formation in the temperature range 100-200°C. In this type of degradation hydroxyl- and carbonylcontaining groups are formed from the decomposition of hydroperoxide or hydroperoxide radicals. The carbonyl groups are ketonic, resulting from a vinyl ketone initially formed by oxidative attack on the tertiary hydrogen and from a competing attack on α-hydrogen. The interaction of the product of the latter competing reaction forms an intermediate, the decomposition of which requires an activation energy of 18 kcal./mole and yields a carbonyl and hydroxyl group. The radicals and hydroperoxides may also react to give either scission or aggregation. The oxidative products from these reactions give many types of oxygenated groups and radicals.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 315-321 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 425-442 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of propylene polymerization catalyzed by α-titanium trichloride-diethyl-aluminum chloride in heptane diluent were studied. Initiation and transfer processes were followed by using C14-labeled (C2H5)2AlCl. There was no important termination process in this system. The initial C14 activity found in the polymers gave the concentration of active ethyl groups on the surface, [C]. The propagation step was first order in [monomer] and [C], with an activation energy of 13.0 kcal. mole-1; kp at 50°C. was 0.426 ± 0.018 l. mole-1 sec.-1. There were two transfer processes: (1) Rtr1 = ktr1[C] - [(C2H5)2AlCl]1/2, with an activation energy of 18.6 kcal. mole-1, and a value of ktr1 at 50°C. of 6.54 × 10-5 mole-1/2 sec.-1; and (2) Rtr2 = ktr2 [C] [α-TiCl3], with an activation energy of 7.6 kcal. mole-1, and a value of ktr2 at 50°C. of 9.45 × 10-4 l. mole-1 sec.-1. These kinetic data were used to calculate number-average molecular weights M̄n, which agreed well with the ones obtained directly from the C14 specific activity in the polymer. Furthermore, fractionation of four polypropylene samples gave values of M̄n in agreement with those obtained above. At low temperatures, [C] is sensitive to the Al/Ti ratios. This dependence was interpreted as the result of an equilibrium between an active complex containing (C2H5)2AlCl and a much less active complex containing (C2H5)AlCl2. At higher temperatures, [C] is insensitive to the Al/Ti ratios, and polymerization to give amorphous polymers becomes important. Qualitative information was obtained about the processes which give amorphous polymers.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An investigation into the nature of the structural and molecular changes during the bulk oxidation of polystyrene has been conducted by light-scattering and viscometric methods. Oxidations were conducted on films in an air oven at 0, 2, 4, and 5 hr. at 200°C. The oxidized films were dissolved and various parameters obtained on the resulting solutions. Fractionation of unoxidized and oxidized thermally polymerized polystyrene showed a narrowing of the molecular weight distribution during oxidation. The weight-average molecular weight decreased from 1,090,000 to 33,000. That of an unfractionated commercial polystyrene, Styron 683K, decreased from 281,000 to 16,000. These results show that random chain scission of oxidize polymer occurs along with the formation of carbonyl groups giving polymer molecules of shorter chain length most of which probably retain the initial linear random coil structure. In addition to the chain scission, branching and crosslinking are indicated by the distortion of Zimm plots by microgel.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 1839-1856 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method for rapid determination of the nonuniformity coefficient, Mw/Mn, of linear polyethylenes and crystalline polypropylenes is described. The number-average molecular weight Mn was determined by counting the number of C14-labeled alkyl groups introduced into the polymers during the initiation step. The weight-average molecular weight Mw was calculated from viscometric data. The errors in these calculations were estimated. The values of Mw/Mn thus obtained for eleven samples of linear polyethylenes and three samples of crystalline polypropylenes are compared with the corresponding results obtained by polymer fractionations. The agreement was good for all the polyethylene and polypropylene samples studied except for three high viscosity polyethylene samples with high Mw values and low Mn values from fractionation data. The Mw/Mn values were determined for polymer samples taken during ethylene polymerizations initiated by the (C5H5)2TiCl2-(CH3)2AlCl system. This ratio at first decreased with the polymerization time, then reached a minimum as the concentration of growing chains reached a maximum. Comparison of polyethylene produced at various temperatures reveals that the width of polymer distribution decreases with rising polymerization temperatures. This decrease is attributed to the increase in the rates of initiation and termination and the higher activation energy for the termination processes. High catalyst concentrations yielded polyethylenes of broad distributions. At high catalyst concentrations, the concentrations of growing chains are also high. Consequently, more low molecular weight chains terminate early to give products with large Mw/Mn. On the other hand, increase of the Al/Ti ratio increases chain transfers giving polyethylenes having a low Mw/Mn. An additional effect of increasing the Al/Ti ratio is the decreased variation of Mw/Mn with t. The Mw/Mn values of crystalline polypropylene samples taken during polymerizations initiated by α-TiCl3-(C2H5)2AlCl are also presented. They were high at the beginning of the polymerizations and decreased gradually to a lower constant value. At higher temperatures, this variation was less pronounced; and the Mw/Mn values were lower than those for the polymers obtained at lower temperatures. The Mw/Mn values were insensitive to experimental variables such as the catalyst concentrations, the Al/Ti ratios, and the monomer pressures in agreement with the kinetic results. The Mw/Mn values of amorphous polypropylene samples taken during propylene polymerizations did not vary with t or with the other polymerization conditions. These results support the earlier kinetic interpretation that extensive chain transfers occur during the formation of amorphous polypropylenes.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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