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  • 1
    Publikationsdatum: 1977-10-01
    Print ISSN: 0372-820X
    Digitale ISSN: 1435-1536
    Thema: Chemie und Pharmazie , Maschinenbau
    Publiziert von Springer
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 255 (1977), S. 1022-1022 
    ISSN: 1435-1536
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1919-1933 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new phenomenon in necking of some polymers, including poly(ethylene terephthalate) (PETP) was detected. It was found that extension of PETP films under certain conditions results in periodic stress oscillations and a periodic change in appearance of the sample. The conditions at which self-oscillations appear have been determined, and the principal regularities of this regime of deformation are described. The following factors are critical for the appearance of self-oscillation: speed of straining and compliance of the sample. The self-oscillation of stress and formation of the periodic transverse bands is attributed to heat dissipation during necking corresponding to local temperature jumps and periodic strong variation of elasticity modulus due to poor heat conductivity of the polymer. Changing the external conditions of heat transfer influences the possibility and development of the effect. The phenomenon is common for various crystallizing polymers, being dependent on physical properties of the polymer and conditions of deformation.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: New structural phenomena which can be produced in polymers at low temperatures or by the action of high forces are described and discussed. Experimental evidence supports the argument that the deformation of polymers can develop not only as a result of conformational changes of the macromolecules proper but also by transformation of more complex structural formations. The consequence of this phenomenon is the possibility of large deformations far below the glass-transition temperature in a crystalline polymer with well-developed supermolecular structure. This type of deformation takes place without molecular orientation. Another phenomenon discussed is the sharp change of supermolecular structure in crystalline polymers caused by the action of a shock wave. These effects ought to be connected with an energetic rather than entropic deformation mechanism because the transformations occur at a supermolecular level. Thus, there can be two extreme types of deformation processes: the well-known conformation changes that occur at a molecular level, and the deformation of supermolecular structures. Examples of the pure form of the latter type of mechanism obtained under extreme conditions are given.
    Zusätzliches Material: 17 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 95-112 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The viscosity of a number of molten polystyrenes and polypropylenes obtained in various ways from solutions is found to be very strongly dependent on the history of dissolution of the polymer (the concentration of the solution and the “goodness” of the solvent), and on the presence of certain organic oligomeric compounds in very small amounts. The viscosity of the melt may be orders of magnitude less than that of the original samples. The present discussion of these effects is based on the concept of structure formation in amorphous polymers. The structure formed on the solution appears to be very stable with respect to heating and prolonged standing at elevated temperature, although it (and hence the viscosity) strongly depends on the initial concentration of the solution and the nature of the solvent. The role played by additives, present in amounts of small fractions of a percent, is accounted for by the fact that the melt retains the microheterogeneity of the medium. The material moves without its micromosaic structure being disturbed, and the role of the additives is reduced to surface (with respect to structural elements) phenomena.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1139-1154 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Heat effects and structural transformations in amorphous crystallizable poly(ethylene terephthalate) (PET) during uniaxial stretching accompanied by neck formation, have been investigated by calorimetric and x-ray methods over a wide range of temperatures and deformation rates. At small deformation (not exceeding 1-2%) and at temperatures below the glass transition temperature of the polymer, PET behaves as an elastic body. Upon stretching at a constant rate, constant heat power is absorbed, heat effects during loading and unloading coincide completely, and no hysteresis is observed. At large deformations (of the order of 50%), cold drawing develops in this temperature range. The internal energy change in cold drawing is zero within experimental error. A periodic heat release during the self-oscillation regime of drawing PET corresponds to periodic changes in stress, in the rate of the neck formation, and in the appearance of the sample. The temperature limits of the region where crystallization resulting from an uniaxial drawing of the polymer is possible, have been determined, and the heat effect of this phase transition has been measured. Orientation crystallization develops only from 70 to 94°C. These limits are insensitive to changes in deformation rate within one decimal order. The structure of PET in this temperature range has been investigated. The heat of phase transition of orientation crystallization of PET has been determined from the relationship between the measured values of the internal energy change during this process and the limiting degree of crystallinity for the stretched samples. This heat proves to be 5.5 ± 0.1 cal/g.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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