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  • Journals
  • Articles  (65)
  • Wiley-Blackwell  (65)
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (65)
  • 1
    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 characterization of network segment density of elastomers is discussed. Normally equilibrium solvent swelling is used as long as the polymer-solvent interaction parameter χ is available. However, χ is often not known or may be a function of the network segment density, or composition for a polymer whose structure is changed upon aging. The technique of measuring the modulus in tension or compression on solvent-swollen samples allows the network segment density to be calculated from the theory of rubber elasticity. This circumvents the problems associated with the solvent swelling technique. The modification of a commercially available thermomechanical analyzer is described, to enable compression modulus measurements on solvent swollen elastomers to be performed.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. S23 
    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
    Additional Material: 1 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1837-1844 
    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 viscoelastic properties of some polyester-urethanes are compared with the properties of other polymers. The behavior observed is anomalous in that these polyurethanes exhibit an unusually high value of modulus well above their Tg, unaccounted for by either crosslinking or crystallinity. Various experiments including incorporation of plasticizes of widely varying chemical composition have suggested interpretation of the system as a block copolymer, each block having its own Tg. Each of the two types of blocks seems to associate with similar blocks from other molecules.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 3035-3061 
    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 compatibility, morphology, and mechanical properties of poly-∊-caprolactone (PCL) blended with poly(vinyl chloride), nitrocellulose, and cellulose acetate butyrate are described in this study. Methods used in this investigation included differential scanning calorimetry, dynamic mechanical testing, small-angle light scattering, light microscopy and stress-strain testing. Blends of PCL with poly(vinyl chloride) (PVC) are shown to be compatible in all proportions. In the PCL concentration range 40-100%, the PCL crystallizes in the form of negative spherulites. The spherulites were found to be volume filling with as much as 35% PVC. The nitrocellulose blends with PCL exhibited the glass transition behavior of a compatible system over the composition range of 50-100% PCL. At lower PCL concentrations, phase separation was apparent. The PCL crystallinity was present only in the nitrocellulose blends with more than 50% PCL, and it was in the form of rod-like super-structures. Blends of PCL with cellulose acetate butyrate were shown to be phase separated, with one phase having nearly equal proportions of the two polymers. The PCL crystallinity was in the form of negative spherulites and was formed with PCL compositions as low as 50%. Stress-strain results show polycaprolactone to be an effective plasticizer for poly(vinyl chloride) and the cellulose derivatives studied.
    Additional Material: 17 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 201-214 
    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 diffusivities of simple gases through a series of polyurethane block copolymers of differing aromatic urethane content and type of soft segment were measured using a quadrapole mass spectrometer as a detecting device. Although an Arrhenius expression generally described the temperature dependence of diffusion in this system, a discontinuity was observed in the Arrhenius plots for some materials, and the discontinuity was found to be related to the onset of the glass transition in the hard domains. Increasing the hard segment content of the materials decreased the diffusivity due to the increase in the activation energy of diffusion. Increasing the soft segment length brought about a decrease in the activation energy with an increase in diffusivity. Polyster urethanes had lower activation energies for diffusion than polyether urethanes of similar hard segment composition. Finally, as the penetrant diameter was increased, a decrease in the diffusivity and an increase in the activation energy was noted.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2989-3006 
    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 objective of this research was to study the morphology and properties of PVC-polyurethane blends. Studies on blends of a segmented polyether polyurethane with PVC were carried out utilizing differential scanning calorimetry, Rheovibron, stress-strain, infrared peak position studies, and infrared dichroism experiments. This thermodynamically incompatible system was made kinetically compatible by precipitation from tetrahydrofuran (THF) solutions. THF-dioxane solution casting and melt processing produced an incompatible system. The compatible polyurethane-PVC system contains a well-mixed PVC-polyether matrix phase as evidenced by Tg shifts, orientation characteristics, and infrared peak position changes. The aromatic urethane segments which exhibit microphase separation in the pure polyurethane are not solubilized by blending with PVC by any of sample preparation methods used in this study.
    Additional Material: 13 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4735-4744 
    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: Experimental measurement of the change in coefficient of friction with sliding distance of a carbon-black-reinforced rubber on either glass or Perspex surfaces increases monotonically to a constant value as required by Saibel's theory. However, this general stochastic model does not allow for a fully satisfactory physical interpretation of the effects of run-in on rubber friction. The present measurements for rubber on a glass surface agree well with those of Roth and co-workers reported many years ago. The observation of these effects on Perspex does not appear to have been reported previously. It is found that a material, probably stearic acid or zinc stearate, is deposited from the rubber onto a glass surface when the rubber slides on it.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 2115-2135 
    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 series of polydimethylsiloxane-urea acrylate prepolymers was synthesized by reacting aminopropyl-terminated polydimethylsiloxane (ATPS) with isocyanatoethyl methacrylate (IEM). The oligomers were cured using ultraviolet radiation in the presence of different reactive diluents. Three systems were prepared with varying ATPS soft segment molecular weight. All of the samples were transparent. However, microphase separation was indicated by the observation of two glass transition temperatures attributed to separate ATPS and IEM/reactive diluent phases. Increasing ATPS molecular weight led to a lower rubbery phase transition temperature and a smaller rigid phase volume fraction. These effects were reflected in lower modulus and tensile strength at room temperature, and higher elongation at break. An increase in the reactive diluent content resulted in an increase in Young's modulus and the ultimate tensile strength of these materials. Increasing reactive diluent content caused the rubbery phase transition peak to decrease in magnitude without changing its position and shifted the hard segment transition to higher temperature. The tensile strengths and moduli of these materials were higher than those reported in the literature for other polydimethylsiloxane and urethane acrylate materials.
    Additional Material: 14 Ill.
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  • 9
    ISSN: 0935-9648
    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
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 2-12 
    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 aging and lifetimes of polymeric materials depend on the reaction of these materials to the particular stresses which are applied. In many cases the molecular weight of the polymer is changed and this affords a way to follow aging phenomena. In the simplest case a homopolymer is subjected to a stress which increases or decreases its molecular weight without any chemical changes. As the situation becomes more complicated, changes in chemical composition occur and different sized molecular species are generated. These new species may be of extremely low molecular weight or they may be in the form of crosslinked gel. This paper reviews methods which are available for the determination of molecular weight and molecular weight distribution of polymeric materials. Recently developed or modified techniques are treated in more detail. Techniques which may be used to characterize the oligomer region or analyze for the presence of crosslinked gel are included.
    Additional Material: 24 Ill.
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