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  • 1
    Unknown
    New York, NY : Springer
    Keywords: Polymers ; Surfaces (Physics)
    Edition: Third Edition
    ISBN: 9780387726281
    Language: English
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 4575-4582 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 58 (1985), S. 2822-2830 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Polyethylene single-crystal mats 20 μm thick were heated to the annealing temperatures (120–132 °C) in less than 1 s. The Cornell High Energy Synchrotron Source (CHESS) and a TV detector system were used to obtain wide- and small-angle x-ray scattering patterns from these mats during annealing with a time resolution of 0.3 s. Both whole polymer and a molecular weight fraction showed rapid melting and recrystallization, with a minimum crystallinity at 2–4 s after reaching the annealing temperature. Recrystallization was essentially complete in 60–90 s and most curves could be fitted to the Johnson–Mehl–Avrami equation with exponent n=1. Two-thirds of the material could be molten before there was any loss of the original crystal orientation. The increase in long period was discontinuous at high annealing temperature. The original small-angle long-spacing peak quickly lost intensity as crystallinity fell and a new peak appeared at larger long spacing. This new long spacing increased with time for the whole polymer and was constant for the fractionated material. At lower annealing temperatures the amount melting was small and the small-angle intensity and long period increased continuously.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 381-403 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectra of four gel-spun high-strength polyethylene fibers were recorded as a function of stress, with detailed study of the 1063 cm-1 band. The change in the peak position of this band was linear at low stresses, but there was little change at high stresses. The center of mass of the band moved linearly with stress until fracture, and the shift per unit stress was almost the same for all the fibers studied at 4.0 ± 0.5 cm-1/GPa. The line shape is symmetric at low stresses, and the full width at half maximum increases with stress. When plastic deformation begins the band develops a broad low intensity tail extending to 1000 cm-1. This corresponds to stresses of up to 15 GPa, and the tail contains up to 18% of the band intensity when the maximum stress is applied. Equivalent wide-angle x-ray studies showed no such tail, so the highly stressed material is not crystalline, although it must be in the all-trans form to contribute to the Raman peak. Such load-bearing extended-chain-disordered material is described as taut tie molecules. The amount is much larger than that usually derived from mechanical modelling, it is essentially all the amorphous material if the DSC crystallinity of 85% is correct. It is thought to be interfibrillar, stressed when fibrils slide past each other in creep. On unloading the fiber, the band became more symmetrical again but did not always return to its initial position at zero stress. The peak moved to a wave number greater than its initial value on unloading and then over time relaxed to its original value. Thus tensile stresses in the disordered material, balanced by compression in the crystals, are slow to relax. Lower molecular weight fibers (Mn = 8 × 105) had small anelastic effects, probably because they relaxed within the time of the experiment.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1159-1161 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: No abstract.
    Additional Material: 1 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 41 (1990), S. 2189-2198 
    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 tensile deformation of Kevlar fibers has been studied using Raman spectroscopy. The Raman bands shifted to lower wavenumbers and broadened with stress. The shift of the 1610 cm-1 Raman band per unit stress was about -2.5 cm-1/GPa in both Kevlar 29 and Kevlar 49. A simple one phase paracrystalline model is used to explain the observed shifts. The total increase in the width of the 1610 cm-1 Raman band was about 2.5 cm-1 and the increase in width was negligible till a stress of about 0.5 GPa.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 39 (1990), S. 695-705 
    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: Poly(vinyl alcohol) fibers which were drawn from dried gels were chemically treated with formaldehyde to induce crosslinking in the amorphous phase. The room temperature storage modulus decreased early in the treatment, to an almost constant value of 50-60% of the initial modulus of the fiber. This behavior was independent of the concentration of formaldehyde used. The modulus at low temperature was also reduced, and no Tg peak could be seen in heavily treated fibers. The modulus above the original Tg, 70°C, was much less affected. The crystallinity determined by DSC fell by one third as the room temperature modulus decreased, and X-ray diffraction indicated a reduction in the crystal length along the chain direction at the same time. Thus, under the conditions of treatment used, the loss of properties due to destruction of crystals outweighs the stiffening and reduced water sensitivity of the crosslinked amorphous phase.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 2071-2078 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(vinylidene fluoride), PVF2, has been zone drawn to extensions up to 7 times. Well oriented β phase tapes are produced when the draw neck moved out of the hot zone, at extensions over six times and zone temperatures =〈155°C. Other conditions give α phase tapes. The dynamic mechanical spectra of highly drawn PVF2 is exactly the same for both phases, with Tg at -25°C and a sharp rise in tan δ at 50°C. Isotropic α and β phase sheets gave different mechanical spectra, but with similar features at different strengths. As the isotropic sheets were prepared in very different ways, no specific features of the spectra could be assigned to the different phases.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 2199-2212 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Synchrotron x-ray radiation was used to study structural changes during deformation of a single high-modulus, high-strength fiber of polyethylene (Spectra 1000, Allied Corp.) 20-40 μm in diameter. The high brightness of the synchrotron beam allowed x-ray diffraction patterns to be obtained from 0.5 μg fiber samples in ca. 1 min. The (002) chain axis reflection shifted and broadened when the fiber was loaded in tension. When a model of crystals and disordered material in series was used for the fiber, the measured lattice strain at stresses up to 1 GPa gave a crystal modulus of 250 GPa. At stresses above 1 GPa the (002) reflection no longer shifted with increasing load. A noncrystalline part of the material deforms and takes up the load; this effect has been observed by Raman spectroscopy. The (002) peak also broadens under stress. When fiber bundles were used as samples, broadening could be due to uneven loading of fibers, but with a single fiber sample, one can be sure that the loading at the fiber level is uniform. Broadening of the (002) reflection then indicates inhomogeneities within the fiber. Deconvolution with the line profile of the fiber at zero stress should give the distribution of crystal strains. The strain distributions are symmetric and during loading the full width at half maximum (fwhm) is approximately equal to the mean strain. With an assumed constant crystal modulus this describes the stress distribution as extending from zero to twice the mean stress.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 2509-2523 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The α relaxation of isotropic and drawn poly(vinyl alcohol) dried gel films was studied using dynamic mechanical analysis. The temperature of the relaxation Tα increased from 160°C in the isotropic gel to 220°C in a fiber drawn 19 ×. The relaxation, which is associated with the crystalline regions of the material, also decreased continuously in magnitude as drawing proceeded, although crystallinity increased. At draw ratios over 12 ×, the relaxation became difficult to resolve, and no relaxation was observed in fibers drawn over 19 ×. The melting points of the fibers increased with draw ratio, but not enough to account for the large change in Tα. Crystal thickness in the fiber direction also increased with draw ratio. An analogy is drawn to the case of polyethylene where crystal thickness has been found to control Tα. The absence of a resolvable α relaxation is one reason why it is difficult to draw poly(vinyl alcohol) gels to extremely high ratios.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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