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  • Electronic Resource  (2)
  • 1955-1959  (2)
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  • Electronic Resource  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 22 (1956), S. 184-185 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 471-485 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly-n-octyl methacrylate, prepared by the emulsion technique, was fractionated three times by the fractional precipitation procedure to obtain eight fractions. Relationships between viscosity and weight-average molecular weight were obtained in both an ideal solvent, n-butanol, and a nonideal solvent, methyl ethyl ketone. These relationships are represented by the equations, [η]16.8Θ = 2.68 × 10-4M0.50w [η]23 = 4.47 × 10-5M0.69w, respectively. The effect of the size of the pendant groups (-methyl, -ethyl, n-butyl, -n-hexyl, and -n-octyl ester) on the degree of extension of macromolecules in ideal solvents is discussed. It was found that, initially, as we progress from polymethyl to poly-n-butyl methacrylate, the degree of flexibility of the macromolecule increases as the size of the pendant group increases. These results are believed to be due to the short-range interference effect of the solvent molecule on the degree of free rotation of the macromolecule. However, it was found that poly-n-hexyl methacrylate chains have considerably greater chain extension than any of the other three polymers. This expansion of poly-n-hexyl methacrylate chains is a result of the steric effect of large pendant units. From the results obtained for n-octyl polymer, it is evident that, in spite of further increase in the size of the pendant group by —(CH2)2—, there is a substantial contraction in the n-octyl polymer chain. The reason for this reversal in the polymer chain expansion is not clearly understood at present.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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