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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 159-169 
    ISSN: 0887-6266
    Keywords: polyethylene blends ; phase separation ; fracture toughness ; tensile properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Binary blends of unbranched polyethylene (PE) and 5-10% model ethylene-butene random copolymers are used to determine the effects of composition heterogeneity on phase separation in the melt, semicrystalline morphology, plane strain fracture toughness JC and tensile modulus and yield strength. Slowly cooled samples of melt-miscible blends are appreciably tougher (JC = 5.2 kJ/m2) than unblended PE (JC = 2.7 kJ/m2). A blend with the same average short chain branch concentration, but which is phase separated in the melt state, has JC= 3.3 kJ/m2; dispersed domains of amorphous polymer have little effect on toughness. Enhanced toughness is associated with nonuniform morphology formed on slow cooling “one phase” melts composed of chains with different amounts of branching. The relative number of chemically different chains, as opposed to absolute branch concentrations, seems most important. Tensile properties are relatively unaffected by blending at these levels. Results from these model blends are used to consider the properties of compositionally heterogeneous ethylene copolymers. © 1994 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 557-567 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The proton spin-lattice relaxation times (T1) of melt-crystallized, solution-crystallized, and solid-state-polymerized polyoxymethylene (POM) were measured between -60 and +150°C. The three types of samples each have a pronounced T1 minimum near room temperature which is a high-frequency manifestation of the γ process. From the quantitative dependence of the relaxation intensity on crystallinity as well as from the absolute magnitude of the relaxation times, it is concluded that the γ process in POM arises from hindered rotation of noncrystalline chain segments. The relation between the relaxation times and the long period indicates that these noncrystalline segments constitute disordered lamellar surface layers, the thickness of which depends on thermal history of the material. The temperature dependence of the motion of the relatively thin surface layers of solution crystallized POM is quite straightforward. The γ process in the bulk-crystallized material involves cooperative motion, however, leading to temperature-dependent kinetic parameters.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1749-1756 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polypropylene fibers prepared by quenching in ice-water were drawn at 25, 80, 120, and 140°C to a draw ratio between 6 and 8 at draw rates 0.05, 0.5, 5, and 50 cm/min. The long period increases almost linearly with the draw rate for drawing at 25°C and decreases for drawing at higher temperatures. The effect in the latter cases is an annealing effect. As a consequence of the shorter exposure of the drawn fibers to the high temperature at higher draw rate, the long-period growth proceeds for a shorter time and hence results in a smaller increase of long period. At 25°C, however, the long-period growth is negligible. The increase of long period with draw rate is the consequence of higher adiabatic heating as calculated from the energy input during the plastic deformation which transforms the spherulitic into the fibrous structure. One concludes that the long period established during this transformation depends on the maximum temperature reached in the micronecking zone and not on the macroscopically observed temperature of the sample in the neck.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1023-1045 
    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) patterns of a number of linear polyethylene (PE) and polyoxymethylene (POM) samples have been measured and compared to the intensity functions of one-dimensional paracrystalline lattices. It was found that the ratio of the angular positions of the second and first scattering maxima (θ2/θ1) is generally less than or equal to 2.0, implying that the paracrystalline lattice statistics are symmetric or moderately skewed to larger periods. The Bragg spacing (“long period”) of such samples is within 3% of the identity period of the macrolattice. With quenched POM the ratio θ2/θ1 is substantially larger than 2.0, which indicates either extremely asymmetric lattice statistics or coexisting structures within the material. From consideration of the reduced widths of the first scattering maxima, it was found that some broadening is present in addition to that from the paracrystallinity. This excess broadening could result from a finite lattice length of ∼1000 Å. The need for careful experimental technique for obtaining the actual position of the scattering maximum is emphasized. In addition, it is demonstrated that the scattering curve and the correlation function of the system yield essentially the same apparent structural periods.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 485-500 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Macromolecular chain rupture occurring during tensile deformation of semicrystalline polymers has been investigated by measuring changes in the viscosity-average molecular weight. When interpreted in terms of a random-scission scheme, the observed changes in molecular weight correspond to chain rupture concentrations β ≈ 1018/cm3 for high strength nylon and poly(ethylene terephthalate) fibers. Polypropylene fibers and isotropic samples of polyethylene, polypropylene, and nylon 6 had β ≈ 1016/cm3. The effects of stretching environment and thermal and mechanical history were noted. In all cases, the present study indicated bond rupture concentrations about 10 times larger than those obtained from electron spin resonance (ESR) experiments. The relation between viscometry, ESR, and infrared (IR) estimates of bond rupture and their relevance to mechanical properties are considered.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1329-1354 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small-angle x-ray scattering (SAXS) of isotropic or uniaxially oriented nylon 6 was investigated as a function of thermal and mechanical history. In addition to the peak position and linewidth of the SAXS maximum, the integrated SAXS intensity was measured. It was found that the radial intensity distributions of isotropic or arced patterns are controlled to some extent by the small width of the semicrystalline macrolattice, rendering the conventional long period and line shape analysis inapplicable to these patterns. A two-dimensional analysis is possible with well-oriented fibers; the major structural changes which are seen in fibers after annealing above 190°C are associated with melting and recrystallization. Extensive cold drawing and subsequent annealing cause rather modest (ca. ∼30%) changes in the integrated SAXS intensity. These effects are consistent with the generation of homogeneous interfibrillar regions during the latter stages of plastic deformation. On annealing a quenched film on nylon 6, the transformation of the crystals from a pseudohexagonal to a monoclinic habit occurs above 170°C.
    Additional Material: 14 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 17 (1979), S. 719-723 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1257-1270 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The intensity of the glass transition in semicrystalline polycarbonate was measured by differential scanning calorimetry and by thermally stimulated discharge of electrets. Solution-cast and bulk-crystallized samples possessing widely varying crystallinities and morphologies were investigated. It is shown that the intensity of the glass transition is governed by the extent of primary crystallization and is a linear combination of intensities from the bulk amorphous regions and from noncrystalline polymer within semicrystalline aggregates such as spherulites. The intensity of the glass transition within spherulites is about 0.1-0.3 as great as that in bulk amorphous regions. A three-phase model incorporating two distinct types of noncrystalline polycarbonate is proposed to account for the properties of this polymer.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 1001-1010 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In analyzing the shapes of diffraction peaks from polymers, it has been mistakenly assumed that it is possible to distinguish between models based on “microstrains” and on paracrystallinity. It is shown that either paracrystallinity or distortions due to dislocations give rise to disorder of the second kind and cannot be distinguished by current diffraction methods. Fourier analysis of shapes of peaks from polymers gives quite satisfactory results, despite comments in the literature to the contrary. The analysis can now be carried out with single peaks; multiple orders are not required.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hydrogenation of polybutadienes with from 8 to nearly 100% vinyl content was used to prepare a series of model copolymers of ethylene and butene-1 with uniform microstructures and narrow molecular weight distributions. They range from readily crystallizable to completely amorphous, depending on the frequency of ethyl side branches (2-50 per 100 skeletal carbons). Melting temperature, secondary transition temperature, density, plateau modulus for the melt, and elastic modulus for the solid were obtained as functions of branch content. The effect of crystallinity on the secondary transition and modulus of the solid is discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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