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  • Polymer and Materials Science  (40)
  • Wiley-Blackwell  (40)
  • American Institute of Physics (AIP)
  • Oxford University Press
  • American Chemical Society (ACS)
  • 1980-1984  (35)
  • 1955-1959  (5)
Collection
Publisher
  • Wiley-Blackwell  (40)
  • American Institute of Physics (AIP)
  • Oxford University Press
  • American Chemical Society (ACS)
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 447-455 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nitrosation of nylon 66, with the use of four different nitrosating agents, has been investigated. By the more vigorous nitrosating reactions, heterogeneous nitrosation of nylon yarn occurs rapidly and proceeds to completion in a few hours. In this reaction the amide hydrogen is substituted by a nitroso group to give the structure By heating the nitrosated polyamides, nitrogen is evolved, and polyesters are formed. The kinetics of this change have been fully investigated. Caustic alkali reacts rapidly with nitrosated nylon. Free radicals are produced on exposure of the nitrosated nylon to visible radiation. Partial nitrosation of nylon yarns has been carried out with the use of a running threadline system; the physical properties of the resulting yarns have been examined.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 18 (1980), S. 743-750 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 18 (1980), S. 824-824 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 20 (1982), S. 602-602 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 21 (1983), S. 1005-1010 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 18 (1980), S. 148-148 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    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 26 (1981), S. 1309-1326 
    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 crystalline state deformation of high density polyethylene has been examined at an extrusion draw ratio of 30 over a range of temperatures and pressures. The experiments involve combined pushing (extrusion) and pulling through a conical die. The pressure dependence of the extrusion rate through conical dies is given by a logarithmic relation and the temperature dependence by an activation energy of ∼95 kcal/mole. An equation established for the total applied force linearly relates the pulling and extrusion pressure components and represents a force balance at the die entrance and exit. Steady-state extrusion, with or without pulling, was feasible in a pressure range beyond which fractures occurred owing to strain rate and shear or tensile failure. Under some circumstances the extrusion rate was increased by ten times. The mechanical properties and mode of deformation were not affected by pull load and fibers with a tensile modulus of 55 GPa were produced at T 〈 110°C.
    Additional Material: 14 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4471-4476 
    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: This paper further illustrates the applicability of multiple internal reflectance infrared spectroscopy to the analysis of near-surface photooxidation. The results are compared with transmission infrared spectra to evaluate compositional gradients resulting from photooxidation and the influence of oxygen diffusion. The sample was a solvent-cast film of atactic, narrow distribution polystyrene, Mw of 100,000, that had been drawn to a ratio of 3.0 at 110°C by solid state coextrusion. Irradiation of these thin films, ∼25μm thickness, was performed on exposure to air at 35°C for periods of up to 6 h using a mercury source emitting at 254 nm. On photooxidation, a board peak appears at 3200-3500 cm-1, attributable to hydroperoxide formation. The most dramatic increase in the infrared spectra is found for a carbonyl band at 1730 cm-1. It appears to result from an aromatic acid group since it is shifted to 1660 cm-1 on immersion of the oxidized polystyrene films in aqueous ammonium hydroxide. It is confirmed that the photooxidation of polystyrene occurs preferentially at the surface and that this reaction rate is greatly reduced in the drawn polystyrene film.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2373-2379 
    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: Pure isotactic polystyrene (iPS, Mw = 8.89 × 104, Mw/Mn = 4.89) and its blends with an atactic polystyrene (aPS, Mw = 3.9 × 105, Mw/Mn 〈 1.13) were subjected to draw by solid state coextrusion at 127°C within polyethylene. The content of amorphous iPS in these blends was varied from 100 to 24.4 wt %. The extent of draw-induced crystallization was found to depend on the draw ratio and on iPS concentration. The blend with 24.4% iPS was coextruded in two stages. The highest effective draw ratio (EDR) was 7.6 and 13.7 for one- and two-stage draw, respectively. The highest crystallinity of 33.2% was obtained for pure iPS at the maximum EDR of 7.6. Considerable crystallinity was induced in blends, requiring successively higher draw ratio to reach similar crystallinity with increased aPS content. The tensile modulus increased from 1.5 to 3.2 GPa, independent of iPS concentration. Thermal shrinkage results indicate that the elastic recovery of draw in the blends is near quantitative for an EDR 〈 8. For pure iPS, extrudate elastic recovery was dramatically altered by the draw-induced crystallinity.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 2299-2305 
    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: Because of its possible use as a blocked “post-polymerization crosslinking agent” for polymers containing labile hydrogen, the structure of the acetone oxime adduct of 4,4′-methylenebis-(phenylisocyanate) has been determined. 13C and 1H nuclear magnetic resonance (NMR) spectroscopy has identified this product to be N,N′-(2-propyloximino)-4,4′-methylenebis(phenylcarbamate). Chemical shift assignments were based on information obtained by proton decoupled, off-resonance decoupled, and gated decoupled 13C-NMR, proton-NMR, and semiemperical substituent chemical shift (SCS) parameters.
    Additional Material: 7 Ill.
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