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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 22 (1989), S. 3443-3451 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 11 (1978), S. 879-888 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 11 (1978), S. 101-107 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 12 (1979), S. 354-354 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 5597-5617 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The rheological behavior of partially hydrolyzed poly(vinyl acetate-co-ethylene) (VAE) was investigated, using a Rheometrics Dynamic Mechanical Spectrometer. For the investigation, measurements of storage modulus (G′), loss modulus (G″) and loss tangent (tan δ) of the materials were recorded as functions of temperature at a fixed frequency (i.e., using temperature scans) and, also, as functions of frequency at a fixed temperature (i.e., using frequency scans). For the hydrolysis, three different grades of copolymer (containing 34, 47, 62 mol% of vinyl acetate) were used to yield poly(vinyl acetate-co-ethylene-co-vinyl alcohol) (VAEOH) with varying amounts of hydroxyl group. For comparison purposes, the viscoelastic properties of blends of VAE copolymer with poly(vinyl alcohol) (PVOH), having varying blend compositions, were also measured. The blends were prepared by first mixing a solution of VAE copolymer, which was dissolved in a toluene/dichloroethane mixed solvent, and an aqueous solution of PVOH, and then freeze drying the mixture to a constant weight. Also measured were the glass transition temperature (Tg) of the VAE copolymers and the Tg and melting point (Tm) of the VAEOH terpolymers, using a DuPont Thermal Analyzer equipped with a 910 DSC Module. It has been found that (1) introduction of hydroxyl group into the backbone of the amorphous VAE copolymer has made the resulting VAEOH terpolymer semicrystalline; (2) the Tm, Tg, G′, and the complex viscosity (η*) of the VAEOH terpolymers increase with increasing amounts of hydroxyl group; (3) the physical blending of PVOH with VAE copolymer has not affected the Tg of the VAE copolymer; (4) the G′ and η* of the VAE/PVOH blends are found to increase with the amount of PVOH in the blend. The use of logarithmic plots of G′ versus G″ has been found to be very useful for discerning the differences in the structure of the materials tested.
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 677-701 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelastic behavior and order-disorder transition in mixtures of a block copolymer and a midblock-associating resin were investigated. The block copolymers investigated were polystyrene-block-polysioprene-block-polystyrene (SIS) copolymers (Shell Development Company), specifically Kraton D-1107, with the block molecular weights 10,000S-120,000I-10,000S, and Kraton D-1111, with the block molecular weights 15,000S-100,000I-15,000S. The midblock-associating resin investigated was a resin polymerized from C5 hydrocarbon, referred to as Piccotac 95BHT (Hercules Inc.), which is an aliphatic hydrocarbon containing considerable amounts of cyclic structures, with a weight-average molecular weight of 1,100 and a glass transition temperature Tg of 43°C. In the investigation, mixtures of the block copolymer and Piccotac 95BHT were prepared with toluene as solvent. Temperature scans of the samples were made to obtain information on dynamic storage modulus G′, dynamic loss modulus G″, and loss tangent tan δ, using a Rheometrics dynamic mechanical spectrometer. It was found that Piccotac 95BHT decreased the plateau modulus G0N and increased the Tg of the polyisoprene midblock of the SIS block copolymer in the mixture. This experimental observation led to the conclusion that Piccotac 95BHT associates (or is compatible) with the rubbery polyisoprene midblock of the SIS block copolymer. The order-disorder transition behavior of mixtures of SIS block copolymer and Piccotac 95BHT was also investigated by a rheological technique proposed by Han and Kim (Ref. 21). The order-disorder transition temperature Tr (i.e., the temperature at which the ordered microdomain structure of the block copolymer completely disappears) of the SIS block copolymer decreased steadily with increasing amount of Piccotac 95BHT in the mixture. With the information determined on Tr, a phase diagram for the mixture was constructed, showing the boundary between the mesophase and homogeneous phase in the mixture. The phase diagram is in qualitative agreement with the theoretical predictions of Whitmore and Noolandi (Ref. 28).
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 15 (1977), S. 1163-1175 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The method of sedimentation equilibrium was used to obtain values of the thermodynamic interaction coefficient χ as a function of concentration. Five samples of polystyrene with molecular weights ranging from 36,000 to 1,750,000 were studied in benzene over the concentration range up to the volume fraction equal to 0.03. The experimental data were used to test the theory of Koningsveld et al. (Macromolecules, 7, 73, 1974). This theory predicts that the interaction term in the free enthalpy of mixing may be split into one term common for all molecular weights and another term, which depends on molecular weight and vanishes exponentially at high concentrations. It is concluded that the functional form proposed by the theory gives a fair description of experimental data. However, the phenomenological coefficients obtained from the experiment differ significantly from the values predicted by the theory.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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