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  • Wiley-Blackwell  (34)
  • Oxford University Press  (7)
  • American Society of Hematology  (6)
  • American Chemical Society (ACS)
  • American Institute of Physics (AIP)
  • Annual Reviews
  • 2010-2014
  • 2000-2004
  • 1980-1984  (49)
  • 1955-1959
  • 1984  (13)
  • 1981  (18)
  • 1980  (18)
Collection
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  • 2010-2014
  • 2000-2004
  • 1980-1984  (49)
  • 1955-1959
Year
  • 1
    Electronic Resource
    Electronic Resource
    The Proteolytic Activation Systems of Complement (1981)
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Biochemistry 50 (1981), S. 433-464 
    Details
    ISSN: 0066-4154
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Chemistry and Pharmacology , Biology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1146/annurev.bi.50.070181.002245
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  • 2
    Electronic Resource
    Electronic Resource
    Solution NMR study of the post-polymerization crosslinking agent N,N′-(2-propyloximino)-4,4′-methylenebis(phenylcarbamate). I (1984)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 2299-2305 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1984.070290706
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  • 3
    Electronic Resource
    Electronic Resource
    Solid state extrusion of ultra high molecular weight polyethylene. Processing and properties (1980)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 555-561 
    Details
    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 techniques of solid state coextrusion and powder extrusion have been employed for the deformation of ultra high molecular weight polyethylene. Chain folded and chain extended morphologies obtained under different crystallization conditions were coextruded within a nylon 11 casing acting as a processing aid at an extrusion draw ratio (EDR) of 5 at ≤ 120°C and 0.20 GPa. The powder was compacted and extruded at ≤ 128°C and 0.23 GPa up to an EDR of 24. The physical and mechanical properties of the extrudates were evaluated and found to be dependent on intial morphology. An extrudate from the chain-folded morphology gave a low modulus of 0.71 GPa, the chain-extended morphology a modulus of 6.7 GPa, and the compacted powder a modulus of 15 GPa.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760200808
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  • 4
    Electronic Resource
    Electronic Resource
    Microhardness of extruded high density polyethylene fibers (1980)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 393-395 
    Details
    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 of high tensile modulus has been produced by solid state extrusion using an Instron capillary rheometer. Microhardness measurements on these ultraoriented fibers have been made to assess their perfection from values of the tensile elastic modulus and shear strength. The microhardness tests were measured using a Vickers square diamond. The microhardness increased with the common temperature for crystallization and extrusion, likely due to improvement in the lateral packing of microfibrils. The variation of microhardness with draw ratio is also illustrated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760200603
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  • 5
    Electronic Resource
    Electronic Resource
    A study of the structural integrity of graphite composite structure subjected to low velocity impactPresented at the 35th Annual Technical Conference, 1980 Reinforced Plastics/Composites Institute, the Society of the Plastics Industry, Inc. (1981)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 493-498 
    Details
    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: An analysis for the transient deflections, bending strains, and interlaminar shear stresses in a simply supported laminated composite plate subject to low velocity impact has been obtained using a series solution of the plate governing equations. Results are presented showing the effect of plate geometry and impact location on damage mode. Computed stresses and strain are compared with impact test data to verify, the analysis.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760210809
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  • 6
    Electronic Resource
    Electronic Resource
    Shear degradation of poly(vinyl acetate) in toluene solutions by high-speed stirring (1980)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 173-185 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1980.070250205
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  • 7
    Electronic Resource
    Electronic Resource
    Ultradrawing and crystallization of isotactic polystyrene and blends with atactic polystyrene (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2373-2379 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260723
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  • 8
    Electronic Resource
    Electronic Resource
    Push-pull extrusion: A new approach for the solid-state deformation illustrated with high density polyethylene (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 1309-1326 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260423
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  • 9
    Electronic Resource
    Electronic Resource
    Blends of poly(ethylene terephthalate) and a polyarylate before and after transesterification (1984)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 1629-1638 
    Details
    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: Blends of poly(ethylene terephthalate) (PET) and a copolyester of bisphenol A-terephthaloylisophthaloyl (PAr) (2:1:1) have been studied both before and after transesterification. The physical blends exhibit phase separation in their amorphous states: a pure PET phase and a mixed PAr-rich phase. In spite of this phase separation, PET crystallinity in blends, normalized to PET fraction, surprisingly goes through a maximum at 25% PAr content. The transesterfied copolymers are noncrystallizable and exhibit a single Tg between those of starting polymers, PET and PAr.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1984.070290517
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  • 10
    Electronic Resource
    Electronic Resource
    Ultradrawing of polystyrene by solid-state coextrusion: Shear-induced crystallization in isotactic polystyrene (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2841-2851 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260903
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