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  • 1
    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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  • 2
    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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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 549-568 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As part of a continuing study of ion-containing polymers, a comparison has been made on styrene-based sulfonate ionomers obtained by two different processes. Copolymers of styrene with sodium styrene sulfonate (SSS) have been compared with corresponding polymers obtained by the sulfonation/neutralization of preformed polystyrene (S-PS). The former system covered a range of sulfonate level from 1 to 30 mol %, while the latter ranged from about 1 to 7 mol %. The characterization of these materials has been conducted using solubility behavior, dilute solution viscometry, thermal mechanical analysis, density measurements, and water adsorption studies. At low (ca. 1%) levels the solubility behavior of the SSS copolymers and the sulfonated polystyrenes were similar. However, at higher sulfonate levels the solubility behavior in different solvents and the dilute solution viscometry were significantly different for the two systems. Similarly, thermal analysis studies (DSC) showed that the glass transition of the sulfonated polystyrene increased linearly with sulfonate level, while the Tg for the SSS copolymer increased modestly, up to about 7 mol % sulfonate content, and then remained constant. Significant differences in the softening behavior and water absorption characteristics were also observed for these two classes of ionomers. Although molecular weights and molecular weight distributions are not now available for these ionomers, the differences in their behavior does not appear to be due simply to differences in molecular weight. It is postulated that the differences in the copolymer and the S-PS ionomers may originate with differences in sulfonate distribution. It is suggested that the SSS monomer units are incorporated as blocks in the copolymer as opposed to a more random distribution in the S-PS ionomer. Indirect evidence in support of his argument is found, for example, in the case of the copolymer in the solubility behavior, the relative independence of Tg on sulfonate concentration and the apparent existence of a second, high temperature transition tentatively attributable to an ion-rich phase. Additional studies are required to confirm this hypothesis.
    Additional Material: 14 Ill.
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  • 5
    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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  • 6
    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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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 10 (1972), S. 2397-2407 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyethylene single crystals deformed on copper and NaCl single-crystal substrates by the method of Gleiter and Argon were examined in transmission electron microscopy attached to carbon film carriers constraining them to their deformed state and also after they have been removed from the deformed substrates and were allowed to relax. It was observed that the imposed shear strains can be accommodated by the polyethylene crystals by a combination of debonding from the substrate, elastic flexing, extensive inplane twinning and martensitic shear transformations, buckling, and tearing. No contrast effects suggestive of slip lines could be observed in dark field studies, and the gold droplet decoration technique failed to detect any unambiguous slip lines. From this it is concluded that the critical shear stress for slip is always higher than that for twinning and martensitic shear transformations, and that crystals will deform preferentially by these latter modes.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 10 (1972), S. 2461-2473 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Samples of a phenol-formaldehyde polymer with a deliberately introduced flaw were fractured in tension. The appearance of the fracture surface near the flaw suggested the disruption of particles pre-existing in the polymer. At a greater distance from the flaw, a featureless surface was observed which was succeeded by one showing interference colors. At still greater distances, linear features were observed to be lying in the direction of crack propagation which, in most areas, were regular and evenly spaced. There were indications that these features were formed by the curling of a surface film. The above observations are interpreted as providing evidence that tensile fracture is accompanied by plastic defórmation at the fracture surface.
    Additional Material: 12 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1949-1961 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cast samples of a phenol-formaldehyde polymer with a crack of length defined by a metallic foil inclusion were fractured in tension. The stress at fracture was inversely proportional to the square root of the crack length, in agreement with the Griffith equation for brittle fracture. The behavior did not conform to the Griffith equation with respect to the experimental value of surface free energy, which was several orders of magnitude higher than a theoretically calculated value. However, as the temperature of tensile testing was raised, the experimental value did approach the calculated value. Consistently the appearance of the fracture surface was observed to change from one showing evidence of plastic deformation at room temperature to a featureless appearance, characteristic of brittle fracture, at higher temperatures.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 557-560 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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