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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1113-1125 
    ISSN: 0887-6266
    Keywords: polyethylene ; tensile necking ; plastic instability ; chain orientation ; strain hardening ; strain rate sensitivity ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The development of a plastic instability in a high-density ethylene-butene copolymer under tensile drawing was monitored by means of a video-controlled optical extensometer in order to study the mechanism of initiation and propagation of necking. True-stress true-strain curves measured along the neck at various times of the drawing are compared with the curve recorded as a function of time at the locus where the neck started. A strain rate gradient is shown to build up during the stage of neck initiation. Evidence is given of tensile normal stress in the concave part of the neck shoulder. X-ray diffraction reveals an oblique preferred orientation of the crystal c-axis that is governed by the lower energy-consuming pathway for the deformation. This is responsible for the plastic flow localization owing to an improved shear ability. The gradual c-axis orientation towards the draw direction as the neck grows involves a strain-hardening effect that leads to neck stabilization. The conclusion is put forward that neck propagation lies in the gradation of the preferred orientation along the neck shoulder rather than in stress triaxiality. Comparison with a parent low-density copolymer shows a better trend for oblique preferred orientation of the c-axis and a reduced propensity for localized plastic flow thanks to a more homogeneous distribution of the stress over the crystallites. © 1996 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 4 (1983), S. 417-421 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2151-2164 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: EPDM terpolymers with ethylidene norbornene as diene monomer could be prepared by means of a soluble Ziegler catalyst formed from biscyclopentadienyl zirconium dimethyl and methylaluminoxane. The overall activities lie between 100 and 1000 kg EPDM/(molZr h bar), obtainable at zirconium concentrations as low as 5 × 10-7 mol/L. After an induction period (0.5-5 h) the polymerization rates increased and then leveled to a value which was constant for several days. From copolymerization kinetics reactivity ratios r12 = 31.5, r21 = 5 × 10-3, and r13 = 3.1 could be derived, and by 13C-NMR spectroscopy r12 · r21 = 0.3 was found (1: ethylene, 2: propylene and 3: ethylidene norbornene). The regiospecifity of the catalyst toward propylene leads exclusively to the formation of head-to-tail enchainments. The diene polymerizes via vinyl polymerization of the cyclic double bond, and the tendency to branching is low. Molecular weights were estimated between 40,000 and 160,000. The average molecular weight distribution of 1.7 is remarkably narrow. Glass transition temperatures of -60 to -50°C could be observed. The cure behavior and the physical properties of cured samples were also tested.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    International Journal of Numerical Modelling: Electronic Networks, Devices and Fields 11 (1998), S. 307-316 
    ISSN: 0894-3370
    Keywords: Engineering ; Numerical Methods and Modeling
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: This paper presents an FE modelling approach for the calculation of transient eddy currents in thin conductive layers, where the complexity of the geometry prohibits both a detailed FE modelling and the use of analytical tools. The method allows an estimation of the maximum values of eddy currents at a highly reduced modelling effort and the use of a commercial FE software package. A prerequisite is a slowly varying magnetic field that can be assumed to be unaffected by the eddy currents. It is shown that neither the source of the magnetic field nor the insulating environment has to be modelled. The model is built up exclusively from 2D elements and is excited via the magnetic vector potential. The spatial distribution of the latter is calculated separately in a magnetostatic calculation based on Biot-Savart's law. It is then applied in time-varying form as a dynamic boundary condition at every node of the model. The method was applied to a simple problem for which the results of a detailed FE calculation were available, to document its validity. Further numerical results are presented for the plasma vessel and the heat radiation shield of the Wendelstein 7-X fusion experiment in the case of an emergency discharge. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2151-2159 
    ISSN: 0887-6266
    Keywords: ethylene/butene copolymer ; tensile deformation ; volume change ; mechanical relaxation ; Raman spectroscopy ; mesomorphic phase ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This article deals with the characterization of the structural changes induced by uniaxial extension in the amorphous phase of an ethylene/butene copolymer. Volume change measurements indicate a reversible densification relevant to a strain-induced organization in the amorphous phase. The dynamic mechanical behavior shows an improvement of the β relaxation that reveals an important immobilization of the amorphous chains. The vibrational behavior investigated by means of Raman spectroscopy suggests that the strained amorphous chains are structurally analogous to the mesomorphic interfacial component. A discussion is made about the mechanism of the transformation of the amorphous phase into a mesomorphic structure compared to the more common strain-induced crystallization phenomenon. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2151-2159, 1997
    Additional Material: 6 Ill.
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