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  • 1980-1984  (5)
  • 1
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A small-angle neutron scattering method is presented for the determination of single-chain scattering functions in heterogeneous two-phase polymeric materials such as incompatible polymer blends and microphase-separated diblock copolymers. Development of the method makes use of both the discrete and continuum approaches to scattering theory. In this fashion it is shown that extraction of the single-chain scattering function requires only two experimental observations, regardless of the compressibility of the system. These experiments consist of small-angle neutron scattering profiles from two samples: an unlabeled two-phase material and a similar two-phase material in which a portion of the molecules in one phase have been replaced by molecules which are contrast labeled by isotopic deuterium substitution. Anticipated difficulties associated with actual application of the procedure and requirements of the necessary experimental samples are discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1439-1472 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The small-angle x-ray scattering (SAXS) technique has been used to characterize the detailed microphase structure of two crosslinked segmented polyurethane elastomers. Both copolymers contain trifunctional polypropylene ether triols in the rubbery elastomeric block, but are synthesized with different hard segments: a symmetric 4,4′-diphenylmethane diisocyanate (MDI) chain extended with butanediol (BD); and an 80/20 mixture of asymmetric 2,4-toluene diisocyanate (TDI) and symmetric 2,6-toluene diisocyanate (TDI) chain extended with ethylene glycol (EG). Calculations of SAXS invariants and determinations of deviations from Porod's law are used to examine the degree of phase segregation of the hard- and soft-segment domains. Results show that the overall degree of phase separation is poorer in the asymmetric TDI/EG-based copolymer than in the symmetric MDI/BD-based copolymer. Determination of diffuse phase boundary thicknesses, however, reveals that the domain boundaries are sharper in the asymmetric TDI/EG system. The contrasting morphologies found in the two systems are interpreted in terms of differences in hard-soft segment compatibility, diisocyanate symmetry, and diisocyanate length. Coupled with conformational considerations, this information is used to construct a new model for polyurethane hard-segment microdomain structure. Important features of the model are that it takes into account the effects of hard-segment sequence length distribution and allows for folding of the longer hard-segment sequences back into the hard-segment domain.
    Additional Material: 24 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 2181-2200 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The diffuse phase boundary thicknesses of two segmented polyurethane block copolymers have been determined by small-angle x-ray scattering analyses of deviations from Porod's law. A self-consistency test of these measurements is performed by comparing results of experiments carried out under a variety of collimation geometries, and using a number of different analytical procedures. Self-consistent values of the diffuse phase boundary thickness are obtained for both of the materials examined. The discrepancies between these values and previous literature values are discussed and possible origins of these differences are presented.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 24 (1984), S. 293-310 
    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 morphology of two series of polyurethane/polyvinyl interstitial composites is characterized by scanning electron microscopy, small-angle light scattering, and small-angle X-ray scattering. Thermal and mechanical properties are measured using differential scanning calorimetry and dynamic mechanical analysis. The polyurethane networks examined are microphase separated segmented block copolymers. A variety of linear and network vinylic components are studied including polymethacrylonitrile homopolymer and copolymer, and polyacenaphthalene homopolymer and copolymer. The polyurethane and polyvinyl components phase separate during the in situ polymerization resulting in a three-phase morphology. Detailed small-angle X-ray scattering analysis provides measurements of phase mixing, domain spacings, and diffuse phase boundary thicknesses. A comparison of these parameters for parent polymers and composites reveals only slight differences; indicating that the microdomain structures of the phase-separated polyurethane networks are preserved in the composite. Appreciable molecular interpenetration of components is not observed. Dynamic mechanical loss measurements for several of the composites demonstrate the presence of loss processes occurring over extremely broad ranges of temperature. The strong mechanical interaction between components observed suggest that the urethane and vinyl phases may be bicontinuous in these materials.
    Additional Material: 27 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An extension of Hartel's theory for multiple scattering has been applied to the case of small-angle light scattering from polymer films with random two-phase morphology. The scattering is treated in terms of Debye-Bueche theory from which values of the correlation length, an average phase size, and mean-square fluctuation in polarizability are determined. It is shown that multiple scattering leads to a reduction in the angular dependence of scattering due to an enhancement of scattering at high angles. This leads to an underestimate of the correlation length and an overestimate of the magnitude of the mean-square polarizability fluctuation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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