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  • 1970-1974  (11)
  • Chemistry  (11)
  • multicomponent
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 2317-2319 
    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 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 3041-3046 
    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: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 10 (1970), S. 177-184 
    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: Increases in modulus, tensile strength, and swelling caused by reinforcing silicone rubber with silica filler were correlated with the thermoelastic parameter, fe/f. A new semiempirical equation of state, containing a generalized front factor, was derived to explain the experimental results. While the retractive force in pure gum elastomers is largely entropic in origin, reinforcement in silicone rubber-silica systems appears to arise by greatly augmenting the deformational free energy change stored in energetic modes.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 12 (1972), S. 101-108 
    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: Interpenetrating polymer networks (IPN's) of polybutadiene (PB) and polystyrene (PS) were prepared using both random (containing 36% cis, 55% trans, and 9% 1,2 vinyl) PB and high-cis PB. For both series, a wide range of PB/PS compositions were synthesized. Using samples stained with osmium tetroxide, electron microscope studies revealed an irregular cellular structure of a few hundred Ångstrom diameter with the first component, PB, making up the cell walls. The size of the cells was found to depend on the PB crosslink density for the random materials. Modulus-temperature data revealed two distinct glass transitions, confirming the microscopy finding of two phases. However, the transition temperature and transition slope varied with composition, and with the microstructure of the polybutadiene, giving evidence of significant molecular mixing. Stress-strain data on the IPN's showed that materials rich in PB behave like self-reinforced elastomers. Charpy impact resistance experiments on materials rich in PS indicated values of 5 ft-lb/in. of notch, which compares well with graft-type polyblends of similar PB/PS composition. The results were interpreted in the light of the recent theoretical work of Bragaw, who considered the importance of the distances between domain boundaries with respect to crack acceleration mechanics. Although the IPN's considered herein exhibited somewhat less than the predicted optimum phase dimensions, the arrangement of the domains is different from ordinary impact resistant plastics.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 2785-2796 
    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: Light-scattering and optical microscope observations of silica-reinforced silicone rubber have shown that the filler is dispersed in a complex manner. Much of the original material appears agglomerated into particles several microns in size. These particles apparently further cluster to form agglomerates of about 20 μ in diameter. In an earlier paper in this series it was shown that the thermodynamic function fe/f (the fraction of the retractive force due to internal energy changes) was a measure of the reinforcement level. It is now proposed that the corresponding physical mechanism of reinforcement may have its origin in the large amounts of energy required to deform the filler particle agglomerates.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 73-78 
    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 interpenetrating polymer networks were prepared containing PMMA and PEA as their two components. Corresponding telomer mixtures and random copolymers were also prepared for comparison purposes. The glass-rubber transition studies were made via shear modulus and dilatometric measurements. The results indicate one very broad transition for the IPN's rather than two transitions expected for incompatible polymer pairs. An interpretation based on the compatibility or near-compatibility of the PEA/PMMA pair is offered.
    Additional Material: 4 Ill.
    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 17 (1973), S. 3811-3814 
    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 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 913-923 
    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: Using a modified interfacial polymerization route, a graft copolymer of nylon 6,10 and polystyrene was prepared. First, an aqueous suspension of styrene monomer was encapsulated with nylon 6,10, followed by polymerization of the styrene to form the graft copolymer. When the material was subsequently molded below the crystalline melting point of nylon 6,10 (220°C), modulus-temperature behavior intermediate between polystyrene and nylon 6,10 was observed. However, when this graft copolymer was molded above the melting point of nylon 6,10, behavior more like pure polystyrene was observed. Phase contrast microscopy revealed that material molded below 220°C showed a continuous cellular-phase structure of about 30 microns in diameter, the interior of the cells being composed of polystyrene and the cell walls being composed of nylon 6,10. Phase inversion phenomenon was observed in the graft copolymer as the molding temperature was raised above 220°C. The nylon 6,10 phase became discontinuous, small globules being formed. This behavior is analogous to spheroidization in steel. It is thought that molten nylon 6,10 spheroidizes to attain a lower surface-energy state.
    Additional Material: 8 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 14 (1970), S. 2815-2824 
    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 creep behavior of a series of poly(ethyl acrylate)-poly(methyl methacrylate) interpenetrating polymer networks was investigated. For comparison purposes, some stress relaxation data were included. Master curves containing a single broad transition covering approximately 20 decades of time were found for midrange compositions. Although the time-temperature superposition principle and the WLF equation should not strictly apply, reasonable agreement was found over a large portion of shift factor versus temperature plots. Application of a modified Tobolsky-Aklonis-Dupre glass-rubber theory suggested that the breadth of the transition could be attributed to a near continuum of phase compositions in the material, each phase composition making its specific contribution to the relaxation spectrum. Whether or not these phase regions are so small as to arise from random concentration fluctuations in an otherwise compatible polymer pair remains unknown.
    Additional Material: 11 Ill.
    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 17 (1973), S. 2443-2455 
    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: Interpenetrating polymer networks (IPN's) of poly(alkyl methacrylates) and poly(alkyl acrylates) have been synthesized in latex form. Dynamic mechanical spectroscopy studies on these materials revealed extraordinarily broad glass transition regions, illustrating the semicompatible nature of these materials. In a true synergistic effect, the value of tan δ remains high and nearly constant over a broad temperature range for select compositions, emphasizing their potential value in noise and vibration damping applications. Compositionally identical latex IPN pairs were prepared by slow and rapid addition of monomer. The mechanical behavior of the resulting materials was similar and can be explained in terms of the core-shell model. A 50/50 isomeric homologous series of compositions was examined. After taking into account the relative difference between the glass transition temperatures of the methacrylic/acrylic pair, no substantial change in compatibility was noted throughout the series. Because the acrylic monomer II is roughly equally solvated by both the previously formed methacrylic polymer I and the nascent acrylic polymer II, extensive polymer I/polymer II mixing is encouraged, and sharp phase separation discouraged in these materials.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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