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  • 1980-1984  (9)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 13 (1980), S. 399-409 
    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
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 371 (1981), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 24 (1984), S. 1138-1141 
    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: Cylindrical specimens of poly(methyl methacrylate) (PMMA) were quenched from above the glass transition and subsequently tested in torsion. Torque and normal-force relaxation responses were recorded simultaneously. The experiments were performed at 40, 60, and 80°C, at increasing aging times and at deformations ranging from γ = 0.0027 to γ = 0.074. It was found at 40 and 60°C, that, contrary to the classical picture of aging, the small-deformation torque-relaxation curves could not be superposed by any combination of vertical and horizontal shifts. On the other hand, at 80°C, and in the nonlinear deformation range even at lower temperatures, the relaxation curves are superimposable simply by horizontal shifts, but as γ increases they involve decreasing values of the double-logarithmic shift rate. At the same deformation level, however, the shift rate for the normal force is significantly higher than is that for the torque over most of the γ range investigated.
    Additional Material: 5 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. 1087-1103 
    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 response of glass-forming systems to isobaric three-step thermal cycles involving cooling, isothermal annealing, and subsequent reheating has been investigated comprehensively using numerous combinations of the experimental and material parameters. The latter include the retardation spectrum or response function and the parameter x which determines the relative contributions of temperature and structure to the retardation times. The results show that, on heating, multiparameter systems can display three kinds of peak in the expansion coefficient α or the heat capacity Cp originating from the interactions of the elementary retardation processes with the thermal history of the glass. The conditions under which these peaks occur, their shifts with x, and the experimental variables have been investigated in detail. In particular, it has been shown that for a thoroughly stabilized glass reheated rapidly, the temperature at which the main peak occurs is strongly dependent on the experimental variables and on x, and that this dependence can lead to an estimate of the value of x. For poorly stabilized glasses reheated slowly, on the other hand, the main peak apparently vanishes and allows an upper peak to appear, which is small and insensitive to x and the experimental variables. Intermediate situations in which the main and the upper peaks occur separately give rise to a range of effects which may become quite complicated as the two peaks approach each other. The occurrence of such multiple peaks, which has usually been overlooked or misinterpreted in the past, is discussed and explained in detail and is compared with some experimental observations reported in the literature.
    Additional Material: 19 Ill.
    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 26 (1981), S. 2665-2677 
    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 formation of a polymer/polymer composite by solid-state polymerization of trioxane (TOX) crystals grown within binary trioxane/polycaprolactone or trioxane/poly(oxythylene) mixtures is reported. At present, such composites have been formed with trioxane-rich (hypoeutectic) mixtures. It is observed that in this composition range, much higher yields are obtained through thermal orientation of the TOX crystals which result in very highly ordered systems as revealed by optical and electron microscopy. These POM-rich composites were not, however, amenable to mechanical testing.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2485-2500 
    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 solid-state polymerization by γ-radiation and postpolymerization of bulk samples of trioxane has been investigated. Different thermal treatment results in radically different initial morphologies of the melt-crystallized trioxane which in turn have a profound influence on the yield and morphology of the resulting poly(oxymethylene) (POM). The polymerization yield increases in the following series: melt-crystallized trioxane with an “opaque” (small grains) morphology, as-grown needles, trioxane with a “quasi-transparent” morphology, and finally thermally oriented crystals. Furthermore, little additional POM is formed during repeated polymerization cycles. The observation of an extensive nodulation of the polymer fibrils when the yield is high is consistent with a multiple-stage growth model for the solid-state polymerization of trioxane.
    Additional Material: 13 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 20 (1982), S. 1341-1353 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A number of characteristic liquid-crystalline textures can be obtained in binary and ternary systems (i.e., including one or two solvents) based on polystyrene-poly(ethylene oxide) (PS-PEO) and polystyrene-polyisoprene block copolymers. These textures include oily streaks, myelinic figures, and vesicles, all characteristic of a lamellar structure; fan-shaped textures of cylindrical structure; and isotropic domains indicative of a cubic structure. Experimental conditions used to systematically produce the mesomorphic textures are described, and the rather critical solubility conditions which the solvents must meet are indicated. The rules and described procedures should be quite general and applicable to other copolymers as well. Finally, highly unusual examples of “pseudomorphosis” typical of liquid-crystalline textures occurring in bulk upon melting and crystallization of the PEO sequences in PEO-PS copolymers are also reported.
    Additional Material: 11 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 22 (1984), S. 1655-1696 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The behavior of the multiparameter KAHR model (put forward by Kovacs, Aklonis, Hutchinson, and Ramos) has been investigated using a single-box retardation spectrum to describe the kinetics of volume and enthalpy recovery of glasses in three-step thermal cycles involving colling, isothermal annealing, and subsequent reheating. It has been shown that during the heating stage, the system may display up to three peaks in the expansion coefficient and the specific heat. The shifts of the peak temperatures Tp with respect to each of the four experimental variables Yi defining the thermal history are analyzed systematically in terms of a set of reduced variables, scaled by two of the material constants of the system. These shifts, from which the various partial derivatives (∂Tp/∂Yi)j≠i are estimated, are determined for five values of another material parameter x, which characterizes the relative contributions (O ≤ x ≤ 1) of temperature and structure to the retardation times. the results show that the upper peak is always small and is insensitive to the characteristics of the spectrum and to the value of x, while the relevant peak temperature depens only slightly on the cooling and heating rates. On the Other hand, the magnitude and the shifts of the main peak depend on all the experimental variables and the material constants in a rather complex manner. It is shown, however, that in limiting situations, involving fast heating of well-stabilized glasses, the shifts of the relevant peak temperature T̂all reduce to a linear function of x-1. since this relationship is rather insensitive to the shape of the spectrum, the experimental determination of any one of the nonzero partial derivatives of T̂ provides a simple means for an independent estimate of the value of the important material constant x. Finally, the shifts of the upper and main peaks relative to each other will be analyzed in terms of the pertinent experimental variables and compared with actual data reported in the literature for polymer glasses.
    Additional Material: 15 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 21 (1983), S. 2419-2424 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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