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  • American Institute of Physics (AIP)  (2)
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 3894-3904 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have investigated the thermodynamic interactions as functions of component volume fraction φ and temperature T in six binary polymer blend systems. The components in all cases were model polyolefins, made by saturating the double bonds of nearly monodisperse polydienes. Small-angle neutron scattering measurements for single-phase melts, analyzed with the incompressible random phase approximation, were expressed in terms of the Flory–Huggins interaction parameter χ for 27 °C≤T≤167 °C and 0.1≤φ≤0.9. In most systems we found a characteristic upturn in χ at the composition extremes that diminished with increasing temperature. We also found that the component chain dimensions were unaffected by the strength of the interactions. Several theoretical attempts to explain the dependence of χ on component volume fraction were examined. Most were qualitatively inconsistent with the results, and none were fully satisfactory.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 3905-3910 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Partially deuterated polymers, made by saturating the double bonds of polydienes with deuterium, have been found to produce weak but significant coherent patterns in small-angle neutron scattering (SANS) experiments. The results suggest the presence of slight differences in deuteration levels among the chains. The scattering profiles for such materials and for blends containing them were calculated with the multicomponent random phase approximation (RPA). The coherent intensity for the deuterated component alone is predicted to be proportional to the variance of its scattering length distribution and to have a q dependence corresponding to the pure component structure factor. The SANS data for a variety of partially deuterated polyolefins are shown to be consistent with these predictions. The theory also predicts that the scattering from their blends with an hydrogenous component is enhanced by this scattering length inhomogeneity, that the enhancement is additive, and that the conventional two component RPA may be used to analyze the data after this contribution is subtracted. Experimentally, we find that uncorrected scattering from blends rich in such deuterated components lead to anomalous estimates of chain dimensions and thermodynamic interactions. The anomalies disappear when the proposed correction is applied.
    Type of Medium: Electronic Resource
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