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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 14 (1976), S. 749-757 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Styrene-acrylonitrile (St-AN) copolymers of three compositions - 27.4 mole-% (SA1); 38.5 mole-% (SA2); and 47.5 mole-% (SA3) acrylonitrile - and styrene-methyl methacrylate (St-MMA) copolymer (SM) of 46.5 mole-% methyl methacrylate were prepared by bulk polymerization at 60°C with benzoyl peroxide as the initiator, and were then fractionated. The molecular weights of unfractionated and fractionated samples were determined by light scattering in a number of solvents. The [η] versus M̄w relations at 30°C were established for SA1, SA2, SM, and polystyrene (PSt) in ethyl acetate (EAc), dimethyl formamide (DMF), and γ-butyrolactone (γ-BL), and for SA3 in methyl ethyl ketone (MEK), DMF, and γ-BL. Second virial coefficients A2 and the Huggins constant were determined. From values of A2 and the exponent a of the Mark-Houwink relation it is seen that the solvent power for samples SA1, SA2, and PSt is in the order EAc 〈 γ-BL 〈 DMF, while for sample SA3 the solvent power is in the order MEK 〈 γ-BL 〈 DMF. The solvent power decreases with an increase in AN content. The solvent power of the three solvents used for SM copolymer sample is practically the same within experimental errors. From the a values it is concluded that in a given solvent the copolymer chains are more extended than the corresponding homopolymers.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 277-282 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ethyl acrylate (EA) and n-butyl methacrylate (n-BMA) copolymers were prepared in solution and the composition of the copolymer samples was estimated by 1H-NMR spectroscopic techniques. Because the characteristic signals, which vary with the composition of the copolymer, were absent, the ratio of intensities of down-field protons to that of the total protons was used for the estimation of copolymer composition. Reactivity ratios were calculated from these values by using the Kelen-Tudos differential linear equation.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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