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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 3037-3042 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It was reported earlier that the copolymerization of acrylamide and styrene is strongly affected by the copolymerization medium. The effect was attributed to a change in the polarity of the ethylenic bond in the acrylamide monomer due to hydrogen bonding and/or dipole - dipole interaction, depending on the medium. In view of those findings, it was suggested that absolute values for the reactivity ratios for the copolymerization of these two monomers might be obtained only when the acrylamide monomer is unperturbed. Copolymerizations of these monomers at a number of ratios, therefore, were done in benzene, which does not undergo hydrogen bonding and has no dipole moment, at high dilution, when amide - amide interactions between acrylamide molecules should be essentially eliminated. The values of r1 and r2(M1 = acrylamide) were 9.14 ± 0.27 and 0.67 ± 0.08, respectively. There appears to be some indication in this system that high dilution adversely affects the reactivity of the acrylamide monomer while enhancing that of styrene. This aspect requires more study.
    Additional Material: 2 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 12 (1974), S. 133-140 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The spontaneous imidization of acrylamide during polymerization has been studied in three media: benzene, diglyme, and water. The data indicate that neither medium, time, nor temperatures below 140°C cause imidization to occur. The ascription of the low nitrogen found in polyacrylamide by some investigators to imide formation appears to be in error. The low nitrogen is due rather to retained solvent and/or water, for which polyacrylamide has a strong affinity. Imidization may be brought about by strong acids. The solubility of an imidized polyacrylamide decreases with increasing imide content.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 389-398 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition behavior of two sets of ABA poly(styrene-b-isoprene) block copolymers was examined by differential scanning calorimetry. In one series, the triblock copolymers had different total molecular weights and the same (30 wt %) polyisoprene content, in the other, the molecular weight was constant (30,000 g/mol) and the elastomer content was the variable. For all triblock copolymers studied, the data show an inward shift for the glass transition temperatures Tg of the corresponding homopolymers. This shift increases for the rigid-phase Tg as the polystyrene block length decreases. Depending on their molecular characteristics, two, three, or only one Tg were found. The third Tg was interpreted in terms of the existence of an interphase. Some of these conclusions could be confirmed by transmission electron microscopy.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 2217-2225 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structural evolution with temperature of an anionically synthesized ABA poly(styrene-b-isoprene) (SIS) lamellar block copolymer (total molecular weight 45,000; isoprene content 38% by weight) was studied by melt-rheological measurements, electron microscopy, and x-ray and light diffraction. Above 225°C, the dynamic viscosity was found to be independent of frequency up to a critical frequency. The variation of the elastic modulus confirmed the occurence of a transition between 215 and 225°C. For the temperature range considered, all results superimposed well on a two-branch master curve. It was concluded that above 225°C, our SIS behaves like a Newtonian material, whereas for lower temperatures and/or higher frequencies classical non-Newtonian behavior is found. The melt-rheological properties were explained by microscopy and diffraction investigations, which allowed us to follow morphological changes as the temperature was raised. It was found that the two-phase lamellar structure is progressively destroyed, and the transition temperature of 225°C corresponds to the temperature above which complete mixing occurs.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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