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  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 1731-1741 
    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 areas under the linear loss modulus versus temperature curves (loss area, LA) and tan δ versus temperature curves (TA) were evaluated for a number of acrylic, methacrylic, styrenic and butadiene based copolymers and interpenetrating polymer networks, IPNs, as a function of crosslink density and comliosition, and were compared with values predicted by group contribution analysis. The LAs of the sequential IPNs, cross-poly(n-butyl methacrylate)-inter-crosspolystyrene, were found to exhibit up to 30% larger LAs than the poly(n-butyl metacrylate-stat-styrene) copolymers, which had LAs slightly less than the values predicted from the group contribution analysis. At constant chemical composition (50% n-butyl methacrylate, 50% styrene), LA equals 14.4 GPa K for the IPN, attributed to a synergistic effect resulting from the IPN's microheterogeneous morphology, as compared with 10.7 GPa K for the single phase, miscible copolymer. Increases in the LA with increased concentration of polymer, network II were also observed for cross-poly(ethyl acrylate)-inter-crosspolystyrene and cross-polybutadiene-inter-cross-polystyrene IPNs. On the other hand, cross-polybutadiene-inter-cross-poly(methyl methacrylate) IPNs had LAs much lower than were predicted by the group contribution analysis, which were attributed to lower miscibility in this system relative to the other systems evaluated. In general, decreased crosslink densities and lower concentrations of network II increased TA. These findings demonstrate how the morphology of a multiphase polymeric material can affect LA and TA, with significant increases In damping capability over the average of the component polymer values.
    Additional Material: 13 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 53 (1994), S. 1425-1434 
    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: Semi-interpenetrating polymer networks based on two elastomers, cis-1,4-polyisoprene (PI) and thermoplastic polyurethane elastomers (TPUs) were prepared in varying compositions. The PI component was cross-linked using peroxide initiators. Modulus and mechanical properties were investigated as a function of composition and temperature. Slight synergisms were observed in mechanical properties, particularly for compositions containing 10% PI by weight. Little or no molecular mixing is shown by differential scanning calorimetry (DSC) for these two-phase materials. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 1379-1390 
    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: Two crystalline melting peaks have been observed by differential scanning calorimetry for low molecular weight poly[3,3-bis(ethoxymethyl) oxetane] (polyBEMO) samples, Mn 〈 1 × 104 g/mol, whereas only one melting peak has been observed for samples of higher molecular weight, Mn 〈 1 × 104 g/mol. Crystallization of low molecular weight samples at large supercoolings produces the lower melting form while low supercooling or annealing favors the higher melting species. Enthalpy of fusion values obtained by DSC for a multiple melting endotherm sample range from 28 to 39 J/g for crystallization temperatures from 58 to 35°C, respectively. Optical microscopy studies indicate that the lower melting peak corresponds to a spherulitic type morphology and the higher melting peak correlates to a fine grained crystal structure. Wide angle X-ray powder diffraction studies do not detect differences in the crystal structures of samples exhibiting either one or two melting peaks, which suggests that the multiple melting phenomenon is due to differences in morphology rather than the presence of different crystal forms.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 1321-1329 
    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: At a constant isothermal crystallization temperature (Tc), the crystalline morphologies of several polymers have been found to be a function of the melt-liquid temperature (T1). At a constant Tc below a critical crystallization temperature (T*c [about 0.9 T*m(K)], a transition from a nonspherulitic to a spherulitic morphology occurs when the melt liquid is heated above a melt-liquid transition temperature, (Tlt) [approximately 1.03 Tm (K)], where Tm is the observed melting temperature of the sample. The melt-liquid transition temperature, Tlt, which experimentally affects the visible morphology of a semicrystalline polymer, is apparently indistinguishable from the thermodynamic melting temperature, T*m, determined by the Hoffman-Weeks procedure. The X-ray powder diffraction patterns of spherulitic and nonspherulitic morphologies were identical, independent of the heating-cooling cycle. This suggests that the transition that occurs at TIt does not affect the arrangement of polymer molecules in the crystallite, but only the manner in which the crystallites are arranged in the supermolecular morphology. The evidence suggests, at least for the polymers studied, that a residual order exists in the melt until the T*m or TIt of the particular polymer is reached. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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