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  • Wiley-Blackwell  (47)
  • American Institute of Physics  (23)
  • American Geophysical Union (AGU)
  • American Chemical Society (ACS)
  • 1975-1979  (70)
Collection
Year
  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 527-532 
    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: Filaments of ultra-oriented high density polyethylene were solid-state extruded at an extrusion (draw) ratio of 26 and subsequently irradiated under vacuum by a cobalt-60 source at doses of 10,15, 20, 40 and 60 megarads (MRad). Several identically prepared but unirradiated strands were also tested. One set of samples at each dose was immersed in a silicone oil bath for one half hour at 128°C and one set was given no post-irradiation thermal treatment. Characterization of the resultant morphologies included differential scanning calorimetry (DSC), birefringence, thermomechanical analysis (TMA), and tensile testing. Results from DSC measurements indicate that initial radiation crosslinking only slightly disrupts the crystal lattice, but on subsequent melting and re crystallization, the chains are unable to recrystallize effectively in their former habit. In all cases, melting point and crystallinity decrease with increasing radiation dose. Birefringence and TMA results indicate that orientation is not disrupted by irradiation. For unannealed samples, Young's modulus increases slightly then levels off while tensile strength and elongation at break increase initially, then drop, For annealed irradiated samples, Young's modulus rises at first, then levels off at higher doses. Tensile strength and elongation at break increase significantly with increasing radiation treatment, then essentially reach constant values at highest doses.
    Additional Material: 10 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 17 (1977), S. 221-221 
    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
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 24 (1979), S. 1371-1382 
    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: Reversible plasticization of nylons with anhydrous ammonia is a new concept. In the present studies, nylons 6 and 11 have been plasticized with anhydrous ammonia and subsequently were solid-state coextruded below the melting point. The plasticization is attained by a temporary disruption of the strong hydrogen bonding between amide groups of adjacent nylon chains. Thermogravimetric and infrared analysis show that for the nylons 6 and 11 the amount of ammonia absorbed is 18% and 10% of the weight of the dry samples, respectively. The ammonia incorporation to preformed nylon ribbons prior to extrusion alleviated significantly the processing difficulties encountered with untreated nylons and aided the rapid extrusion of highly oriented states (EDR 12). The extent of orientation is documented by the high total birefringence values (8.25 × 10-2 for nylon 6 and 5.8 × 10-2 for nylon 11), by the significant increase in crystallinity (23.5%-53% for nylon 6 and 25.7%-40% for nylon 11), and by the enhanced tensile moduli (13 GPa for nylon 6 and 4 GPa for nylon 11).
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 517-527 
    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: Steady shear viscosities, dynamic viscosities and moduli, and the corresponding activation energies for flow were examined for a branched polyethylene, a linear polyethylene, and three of their blends at 150° and 190°C. The polyethylenes were chosen to have closely matched molecular weights and distributions. An R-17 Weissenberg rheogoniometer and an Instron capillary rheometer were used. At lower stress, the branched polymer had a higher viscosity than the linear one, possibly because of the contribution of long branches to entanglements. At high stress, this contribution is reduced and the inherently smaller coil dimensions likely become responsible for the lower viscosity of the branched polymer. The activation energy for the branched polymer is high and decreases with stress, in contrast to the low and almost-constant value for the linear polymer. The effects here of pressure on compression are considered. The entanglements of long branches may also decrease with increasing temperature. With decreasing stress, the activation energy for branched polymer tends to become constant, corresponding to an absence of pressure effects and an equilibrium entanglement of long branches for a given temperature range. The linear relationship between activation energy and blend composition problably means that any compressional effects, like free volume, are additive and that long-branch entanglements rearrange with added linear molecules. The linearity may be the result, in part, of a broad distribution for the lengths of long branches.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 15 (1975), S. 213-218 
    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 general properties of a novel process for producing high modulus polyolefins are discussed. The technique is an extrusion drawing involving a crystal-crystal transformation. The principal tests have been made on polyethylene and the guidelines have been established for extending the technique to other polyolefins. The characterization of such materials is extensively discussed, particularly in the light of the concept of continuous crystals.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 17 (1977), S. 535-543 
    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: Dynamic viscosity and elastic modulus for a low molecular weight styrene-butadiene-styrene (SBS) block copolymer ate measured as a function of temperature (80-170°C) and frequency using the eccentric rotating disc geometry. These linear properties are superimposed to yield master curves each of which exhibits two branches below different (critical) reduced frequencies. At lower temperatures, the non-Newtonian behavior characteristic of SBS block copolymers is observed. In contrast, Newtonian response occurs at higher temperatures. As a consequence, plots of the viscoelastic properties vs temperature exhibit discontinuities below the critical frequencies, reflecting a narrow transition at about 142°C. Above this temperature, it is inferred, consistent with the equality of dynamic and steady state viscosities, that the polystyrene (S) blocks, existent in dispersed domains at low temperatures, exceed a critical degree of compatibility with the continuous polybutadiene phase. The activation energies indicate that the S blocks affect the temperature dependence of the dynamic properties in proportion to their presence in an interphase which is assumed to continuously grow in size as temperature is raised to the transition temperature. Below the critical reduced frequencies, it is inferred that S domain disruption may increasingly occur in conjunction with the observed property enhancement due to these domains, relative to the miscible blocks, as reduced frequency is lowered. However, above these frequencies, the presence of frequency-temperature superposition implies that the S domains and the miscible blocks are equivalent in their effects on properties. At still higher reduced frequencies, the domains present at the low temperatures studied are assumed to remain intact, but plateau behavior similar to the response characteristic of homopolymers is observed.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 537-545 
    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: High density polyethylene has been ultradrawn at 80°C by a novel radial-compression method which involves the gradual buildup of highly-stretched elastic (spandex) filaments around the circumference of a solid polymer cylinder. The sheath of tightly-wound filaments generates a high-radial pressure which forces the polyethylene cylinder to neck down, uniaxially extend, and ultradraw. The physical and mechanical properties of radially-compressed polyethylene of maximum draw ratio, 40-45X, were evaluated and compared with the same polymer ultradrawn in other stress fields. In most physical property categories, the radially-compressed samples are virtually indistinguishable from samples prepared by solid-state extrusion at higher temperature and pressure. The transparency and the maximum tensile modulus, 62 GPa, further confirm the effectiveness of radial compression in achieving ultradraw. An experimental technique for measuring the radial pressure generated by the winding of the highly-stretched elastic filament is presented. The upper-bound pressure in the radial-compression experiments was less than 100 MPa.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 921-922 
    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
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 149 (1976), S. 33-51 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The mature annelid cuticle contains orthogonally oriented collagen in a matrix capped superficially by a dense epicuticle with external corpuscles. The underlying epidermis is a simple columnar epithelium with two major cell types, mucous-secreting cells which secrete through channels in the cuticle to the exterior of the worm, and “supportive” cells which presumably produce and increase the cuticle by secreting into it.The structures of supportive cells, previously interpreted as specialized for establishing interfibrillar collagen order, are revealed by glutaraldehyde fixation as common cellular components without the qualities deemed useful to align collagen. Cell processes which penetrate and sometimes pass completely through the cuticle are not stable, not in geometric order, and lack cilia-like structure. Cilia, unlike the ubiquitous cellular processes, are highly restricted to regions of the epidermis with specialized functions. Cellular control, or other control, of collagen fibrillogenesis remains unestablished.
    Additional Material: 16 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 149 (1976), S. 53-71 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Appearance of collagen fibrils in the cuticle was seen by electron microscopy to be preceded by fonnation of a finely filamentous matrix material. At first, the fine filaments of the matrix are unorganized. However, signs of orthogonal ordering soon appear in the most superficial portion of the cuticle, and subsequently appear more basally and closer to the underlying epidermis. Meanwhile, fibrils of different staining properties and identifiable as collagen begin to be deposited in the superficial portion of the cuticle, the same region which first showed organized fine filaments. Then, like the fine filaments before them, the collagen fibrils polymerize more basally. Collagen appears to polymerize on the preformed skeleton of fine filaments as though the fine filaments caused the collagen to assemble. Neither the polymerization nor ordering of collagen fibrils seems to require direct cellular intervention but occur first in that portion of the cuticle which is furthest away from the underlying epidermis. The fine filaments may be self ordering, extracellular macromolecules which in turn determine the polymerization of collagen fibrils.
    Additional Material: 11 Ill.
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