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  • Wiley-Blackwell  (72)
  • Oxford University Press  (12)
  • American Institute of Physics (AIP)
  • American Chemical Society (ACS)
  • 1980-1984  (74)
  • 1955-1959  (10)
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Years
Year
  • 11
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 1 (1980), S. 1-1 
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 90 (1957), S. 957-962 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Kondensation, welche Catechine unter der Einwirkung von Säuren erleiden, besteht in der Substitution einer reaktionsfähigen CH-Gruppe des einen -Moleküls durch das Kohlenstoffatom 2 (Phenylcarbinoläthergruppe) des anderen. Dieses Ergebnis wird an vereinfachten Modellen aus der Gruppe der Catechine abgeleitet.
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  • 13
    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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  • 14
    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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  • 15
    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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  • 16
    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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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 1439-1445 
    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 surface contact angle of glycerol and of water on polystyrene (PS) films has been found to depend on the extent of uniaxial draw for atactic PS. The contact angle depends on direction for the smooth films of PS drawn by solid state coextrusion. Results as a function of draw ratio to values over 4 on these noncrystalline PS samples, Mw = 6 × 105, have also been interrelated with other measures of orientation such as the anisotropy of surface and bulk properties measured, respectively, by dichroic reflectance infrared spectroscopy and by birefringence.
    Additional Material: 4 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 173-185 
    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: A poly(vinyl acetate) (PVAc) of M̄w 750,000 and M̄w/M̄n 5.10 in toluene solution was sheared in a Virtis-60 homogenizer. The polymer concentration was 3.0 to 12.0 g/100ml, and test temperature was 10 ± 0.5°C. The extent of degradation was measured by gel permeation chromatography (GPC). It was concluded that on shearing (i) the molecular weight decreases rapidly at the beginning of shearing and thereafter decreases ever more slowly toward a limiting value, (ii) the molecular weight distribution is narrowed, (iii) no degradation occurs up to 5000 rpm and thereafter increases with stirring speed, (iv) degradation is more at lower concentrations but concentration is not a sensitive variable, and (v) the chain scission occurs randomly. The Mark-Houwing relationship for PVAc in THF at 25°C was derived as [η] = 2.47 × 10-4 × M̄v0.644.
    Additional Material: 11 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2841-2851 
    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: Polystyrene with a 60% isotactic dyad content (iPS) was subjected to two-stage solid-state coextrusion at 124 and 160°C. It was shown that only shear-induced crystallization occurred with the amount of crystallinity strongly dependent on draw ratio. The steep increase in crystallinity from 0 to 29% is accompanied by a marked increase in the absolute total birefringence from 0 to 30 × 10-3 and the tensile properties, from 2.5 GPa to 4.5 GPa, giving strong evidence for the necessity of a crystalline phase to achieve higher tensile moduli. Wide-angle X-ray scattering showed a higher crystal orientation for the extrudate produced at 124°C than for the one produced at 160°C. Thermal shrinkage experiments support a partial dissipation of orientation after extrusion at 160°C and on reextrusion in general. Electron microscopy revealed a fibrous nature for the solid-state coextrudates produced at both temperatures.
    Additional Material: 10 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 2307-2315 
    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: Nuclear magnetic resonance spectroscopy has been used to study the dissociation and reaction of N,N′-(2-propyloximino)-4,4′-methylenebis(phenylcarbamate), as a crosslinking agent for polymers containing labile hydrogens. The crosslinking of poly(acrylic acid), polyacrylamide, and poly(vinyl alcohol) was found to result upon heating each to 150°C for 10 min with this component at 2-10 wt %.
    Additional Material: 6 Ill.
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