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  • Wiley-Blackwell  (9)
  • Periodicals Archive Online (PAO)  (5)
  • Institute of Physics  (2)
  • Oxford University Press  (2)
  • American Chemical Society (ACS)
  • American Institute of Physics (AIP)
  • American Society of Hematology
  • 2015-2019
  • 1980-1984
  • 1975-1979  (18)
  • 1935-1939
  • 1976  (18)
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  • 2015-2019
  • 1980-1984
  • 1975-1979  (18)
  • 1935-1939
Year
  • 1
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    Cambridge : Periodicals Archive Online (PAO)
    History of science. 14:2=24 (1976:June) 140-141 
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  • 2
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    Detroit, Mich. : Periodicals Archive Online (PAO)
    Technology and Culture. 17:3 (1976:July) 594 
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  • 3
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    Boston : Periodicals Archive Online (PAO)
    Business History Review. 50:1 (1976:Spring) 122 
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  • 4
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    Boston : Periodicals Archive Online (PAO)
    Business History Review. 50:2 (1976:Summer) 229 
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  • 5
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    Berkeley, Calif. : Periodicals Archive Online (PAO)
    California Management Review. 19:2 (1976:Winter) 21 
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  • 6
    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.
    Type of Medium: Electronic Resource
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  • 7
    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.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 16 (1976), S. 200-203 
    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: A study has been made on the effects of molecular weight on the physical and mechanical properties of cold-extruded high density polyethylene. Prior data indicate that such ultra-drawn strands contain a significant fraction of extended-chain crystals. Four samples, spanning the molecular weight range of 59,000 to 147,000, were cold-extruded under the same conditions and were examined with respect to their melting point, degree of crystallinity, linear expansion coefficient, Young' modulus, strain to break, and tensile strength. The degree of crystallinity, linear expansion coefficient, and modulus did not change significantly with molecular weight. The melting point, strain to break, and tensile strength do increase with increasing molecular weight. This leads to the conclusion that the amount of extended-chain crystals is invariant with molecular weight. Higher molecular weight polymers are seen as providing a greater number of the chains, thus giving the fiber a higher tensile strength.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 20 (1976), S. 1199-1208 
    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: Several equations which are used to predict the pressure coefficient of viscosity for amorphous polymers have been examined on the basis of type of information required and equation reliability. These equations can be useful in accounting for pressure effects observed in tubular flow and in other shear geometries. The correlations of Penwell and Porter and of Miller are evaluated and in the perspective of expressions by Matheson and by Eyring. Data on linear amorphous polystyrene (PS), polyisobutylene, poly(vinyl acetate), poly(methyl methacrylate) (PMMA), natural rubber, and polycarbonate are examined and presented. Predictions from the Penwell-Porter and Miller equations are compared with experimental coefficients at one atmosphere for all data available. For PS and PMMA, it was found that Miller's equation tends to predict values somewhat higher than experiments but is closer to the data on PS and on a high molecular weight PMMA. The Penwell-Porter equation, on the other hand, tends to predict values somewhat lower than experiments and does a slightly better job for lower molecular weight PMMA. Both equations require WLF or Vogel coefficients and Tg-pressure-molecular weight data. Miller's equation also requires compressibilities at Tg and at the temperature of interest, although an alternate method can be used which only requires average “K” values without Tg-pressure or compressibilities at Tg.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 20 (1976), S. 1301-1312 
    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: An investigation has been made of the magnitude and the source of degradation of polystyrene in model extrusion experiments. A preformed solid plug of a narrow-distribution, high molecular weight polystyrene (M̄w = 2 × 106) was used for each experiment. The extrusions were performed with an Instron capillary rheometer at constant temperatures from 160° to 220°C. The molecular weight changes occurring in the capillary reservoir during the pass of the capillary and in the hot extrudate were evaluated. Molecular weights and distributions were obtained by gel permeation chromatography. A significant degradation was observed in the capillary reservoir. The degree of degradation was independent of polymer flow. The polystyrene near the walls reacted more extensively than that closer to the axis, but a constant degradation was observed along the axis. The molecular weight profile across the capillary reservoir was attributed to a selective thermo-oxidative degradation (160° and 190°C). Changes in molecular weight due to mechanical degradation in the capillary were observed only at 160°C. This reaction was referred to as a mechano-oxidative process, as no degradation could be detected in the absence of oxygen. At 160°C, selective migration of macromolecules (fractionation) during extrusion did not occur to any significant extent, nor could any thermo-oxidative degradation of the extrudate be detected. When a small amount of antioxidant (Ionol) was added to the polystyrene, no selective degradation did occur at the walls of the capillary reservoir during extrusion at 160° and 190°C.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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