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  • 1
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 microdomain structure of styrene-isoprene A-B type block copolymers having a nearly constant fraction of polyisoprene block segments (13 ∼ 22 wt percent) was investigated by small-angle X-ray scattering (SAXS) as a function of the molecular weights of the copolymers. The styrene-rich block copolymers all have spherical microdomains of polyisoprene block segments dispersed in a matrix of polystyrene block segments. The size of the spherical domains increases with increasing molecular weight of the polyisoprene segment with a power of ca. 0.6. The thickness of the domain-boundary interphase arising from a partial mixing of the incompatible segments at the domain-boundary interface is also estimated by analyzing a systematic deviation of the SAXS intensity distribution from Porod's law at large scattering angles on the basis of the infinite slit-height approximation. The results indicate the interfacial thickness to be about 20Å and to be almost independent of the molecular weight of the block copolymers studied. The applicability of the infinite-slit height approximation in the analysis of SAXS intensity distributions at large scattering angles is also discussed in an approximate fashion.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 24 (1984), S. 361-372 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 dynamic tensile deformation mechanism of spherulitic poly-alpha-olefins, high-density polyethylene, isotactic polypropylene, and isotactic polybutene-1, was investigated by dynamic X-ray diffraction at various temperatures and frequencies in order to assign the α and β mechanical dispersions explicitly. The uniaxial orientation distribution function qj(ζj, 0) of the j-th crystal plane and its dynamic response Δqj′(ζj, 0) in-phase with dynamic strain were observed for several crystal planes, and then the orientation distribution function ω(§, 0, η) of crystallites (crystal grains) and its dynamic response Δω′(§, 0, η), also in-phase with the dynamic strain, were determined by a mathematical transformation procedure proposed by Roe and Krigbaum on the basis of the Legendre addition theorem. The temperature and frequency dependences of Δω′(§, 0, η) were analyzed in terms of a spherulite deformation model combining affine orientation of crystal lamellae with several types of preferential reorientation of the crystal grains within the orienting lamellae. The following assignments are made: (1) the a mechanical dispersion must be assigned to the dynamic orientation dispersions of crystal grains within lamellae involving two types of preferential rotations of the grains associated with lamellar detwisting mostly in the equatorial zone of uniaxially deformed spherulites and with lamellar tilting mostly in the polar zone of the spherulites. Both processes are intralamellar grain-boundary phenomena, and the former process of lamellar detwisting is hardly activated for polypropylene and polybutene-1 spherulites in contrast to polyethylene spherulites. (2) The β mechanical dispersion must be assigned to the dynamic orientation dispersion of the crystal lamellae behaving as rigid bodies unaccompanied by reorientation of crystal grains within the orienting lamellae. This process is an interlamellar grain-boundary phenomenon.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Dynamic x-ray diffraction is employed to scrutinize the structural origin of the α mechanical dispersion of a highdensity polyethylene having preferentially oriented rownucleated cylindritic texture around the machine direction (MD). Results indicate that the α1 dispersion is associated with two kinds of orientation processes of crystallites: (1) the orientation process involving the rotation of crystallites around the crystal b-axis (lamellar axis) dominates in the MD specimen; (2) the other process accompanying the rotation of crystallites or lamellar segments around their crystal a-axis dominates in the TD (transverse direction) specimen. The complex apparent crystal lattice compliances show no frequency dependence in the real component and no appreciable value in the imaginary component, indicating that the α1 process is definitely associated with the intercrystalline process, but not relavent to the intracrystal process. However, at elevated temperatures, the complex lattice compliances exhibit a remarkable frequency dependence, suggesting that the α2 dispersion concomitant to intracrystalline nature takes place in this time scale. The α2 dispersion was found to be more pronounced upon stretching along the lamellar axis (TD) than normal to it (MD).
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
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