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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 2447-2460 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Use was made of differential absorption in the near-infrared region to follow the rates of copolymerization of acrylonitrile (AN, M1) with ethylenesulfonic acid (ESA, M2) in aqueous zinc chloride solution. The concentrations of the monomers were followed separately and simultaneously. It was found experimentally that the ratios d log [M1]/dt and d log [M2]/dt were each constant. This was interpreted to mean that the product of the reactivity ratios of the two monomers (r1,r2) is unity and that the ratio of termination rate constants is equal to the propagation reactivity ratio. It was found that d log [M1]/d log [M2] = r1 = 4.52. This value is in fair agreement with polymer composition data obtained independently. In the Q - e system the equality r1r2 = 1 is equivalent to the monomers having equal e values. Thus, in the AN - ESA system, P1/P2 = k11/k21 = k12/k22 = k1T/k2T, where P1 is the resonance constant of polymer radicals ending in units of M1; and k11, k12, and k1T are the rate constants involving the reaction of this radical with M1, M2, and T (terminating agent), respectively. A gel effect was not observed even at M1 conversions as high as 88%.
    Additional Material: 7 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 481-501 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photolysis of poly(ethylene terephthalate) films was studied in vacuo with light of wavelengths 2537 and 3130 A. A very stable filter system which cuts out the 3025 A. line was developed to isolate 3130 A. from a mercury spectrum. Despite the fact that the penetration of 2537 A. light was limited to a depth of a ca. 103 A. whereas 3130 A. light was more uniformly absorbed it was possible to demonstrate that the quantum yields for CO and CO2 formation were in agreement for the two wavelengths. Quantum yields for fractures and crosslinks were estimated by sol-gel analysis. An absorption maximum which develops near 13 μ after exposure of poly(ethylene terephthalate) to light or γ-rays was attributed to the formation of groups formed by elimination of CO and CO2. ESR spectra for trapped radicals were tentatively assigned to the components p-C6H3· and ·O—CH2—CH2—. It is suggested that the former radicals combine to form crosslinks. Quantum yields (× 104) with 3130 A. light are: CO, 6; CO2, 2; crosslinks, 5.5; trapped radicals, 1.5; With 2537 A. light, quantum yields are: CO, 6-9; CO2, 2-3; the network formed was not characterized as to crosslinks and fractures; trapped radicals were observed to exist but not determined.
    Additional Material: 11 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 1745-1762 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of γ-irradiation on the melting and two solid-solid transitions, occurring near 19° and 30°C, of polytetrafluorethylene was studied by differential scanning calorimetry. A continuous depression of all three transition temperatures, with increasing dose was observed in a first scan of highly crystalline samples at a heating rate of 20°C/min. Additional information was obtained about the accompanying heats of transition. Values for the number of CF2 units excluded from the crystal lattice per 100 eV energy deposition were calculated by using an equation for the depression of the melting point by chemical impurities. The value obtained of G(-units) = 3.3 ± 0.3 is in agreement with a value of G(chemically damaged units) = 3.0 ± 0.1 previously reported on the basis of scavenging techniques. It is concluded that chemical radiation-induced damage in this polymer may be estimated by reference to changes in the melting temperature. A value of G(-units) = 1.6 ± 0.2 was obtained by reference to the 19°C transition.
    Additional Material: 10 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 1167-1171 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 811-818 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methyl methacrylate containing a small amount of 4-methacryloxyethyl trimellitate anhydride (1.0-1.5 wt %) yielded an insoluble network when polymerized in the presence of various inorganic powders, such as lithium aluminum silicate. This unexpected result was obtained for polymerization initiated either by exposure to γ-rays or by heating with azobisisobutyronitrile. In contrast, polymerization in the absence of inorganic powder gave the expected soluble products. Therefore, it is concluded that the inorganic particles play a role in network formation. In order to account for network formation even in a supernatant layer of clear monomer, i.e., above the centrifuged sedimentation volume of the powder, it is suggested that the monomer reacts on the surface of particles to form a diffusive crosslinking agent.
    Additional Material: 1 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 535-548 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The emulsion copolymerization of styrene and sodium styrene sulfonate has been shown to be a feasible preparative route to ionomeric sulfonated polystyrene. The properties of these copolymers are reported elsewhere. The copolymerization rate was found to be dramatically enhanced when compared to that for the emulsion copolymerization of styrene under identical conditions. This copolymerization was studied in detail and two mechanisms were proposed to account for these rate differences. An increase in the number of polymerizing particles in the copolymerization with consequent rate enhancement was substantiated by electron microscopy. However, the data indicate that the rate differences cannot be fully accounted for by this effect. In addition, a gel effect is proposed as a second contributor to the enhanced rate. This gel effect is believed to result from the intermolecular association of the incorporated metal sulfonate units in the growing polymer particles. When a third monomer that plasticizes the ionic interactions is used the polymerization rate decreases. This supports the gel effect hypothesis.
    Additional Material: 12 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2281-2285 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 525-533 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sulfonated polystyrene (S-PS), which is of considerable scientific and technological interest, has been traditionally prepared by the sulfonation of preformed polystyrene. This report describes the preparation and properties of S-PS prepared by emulsion copolymerization of styrene and sodium styrene sulfonate. S-PS prepared by copolymerization gave solubility, solution behavior and thermal characteristics that are consistent with an ionomeric structure. The solubility characteristics indicated some chain-to-chain sulfonate heterogeneity. Thermal analysis studies indicated that the glass transition does not increase with increasing sulfonate content. This is contrary to what has been observed for S-PS prepared by sulfonation and suggests that the S-PS prepared by copolymerization is fundamentally different in structure than S-PS prepared by sulfonation of polystyrene.
    Additional Material: 5 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2137-2140 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 252-254 
    ISSN: 0449-296X
    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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