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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 1383-1395 
    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 mechanical properties of materials prepared by a new method for modifying the structure of polyurethane/poly(methyl methacrylate) (PU/PMMA) interpenetrating polymer networks (IPNs) by using a reactive azo initiator were investigated by means of tensile test, tear test, and dynamic mechanical thermal analysis (DMTA) measurement. The structures of these IPNs were similar to the particulate filled elastomers. It was found that the reactive initiator, which could form blocks of PMMA within the PU matrix (rubber), changed both the filler-matrix interface and the matrix structure. The mechanical properties of these IPNs were dominated by the matrix structure and the interface.
    Additional Material: 14 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 45 (1992), S. 1367-1382 
    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 use of functional azo initiators and the thermal history of the materials have been shown to exert significant effects on the properties of interpenetrating polymer networks (IPNs). The IPNs prepared with a reactive azo initiator from MDI and 1,2-PBD (1,2-polybutadiene diol) with PMMA have been found to exhibit greater ductility, lower rigidity, and lower moduli than IPNs prepared with AIBN. This probably resulted from the attached PMMA blocks modifying the properties of the PU matrix phases. Increasing thermal treatment of IPNs prepared from either the reactive or the normal azo initiators exhibited increased Tg values in both DSC and DMTA scans. These results have been explained by increased association from chemical reactions between the hard segments of the polyurethane and poly(methyl methacrylate) ester groups.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 1397-1409 
    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 tear strength and crack growth mechanism of PBD(1,2)-PU/PMMA (50%) IPN systems were studied by the trouser tear test and single edge notched (SEN) tensile test. It was found that these blend systems showed similar structures and properties to particulatereinforced elastomers. The tear strength was dominated by the structure of the rubber matrix. The PMMA phase increased the tearing resistance by increasing the hysteresis of the IPN systems. Chemical bonding between the PMMA-rich particle and PU-rich matrix prepared by using a reactive azo initiator inhibited the initiation of the fracture nucleus, decreased the intrinsic flaw size, and increased the tear strength. The crack growth of these IPNs was dependent on both the fracture energy available for crack propagation and the hysteresis of the material. The similar structure of these two blends resulted in the similar crack growth behavior.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Most of the reported polymerizations of ethylene at atmospheric pressures utilize heterogeneous catalysts. This paper summarizes some studies of the polymerization of ethylene at atmospheric pressure with nonprecipitate titanium+4 catalyst systems. The nature of the alkyl metal used to make the catalyst influences the occurrence of reduction of titanium which produces the usual heterogeneous state. The highly active alkyl metals must be modified to decrease their reducing power. Electrophilic materials which are normally produced during the reduction step in the Ziegler catalysts must be present to obtain optimum activity of the nonprecipitate catalyst. The homogeneous titanium+4 catalysts described here are more active than the usual heterogeneous Ziegler catalyst. The catalyst formation is explained as due to the formation of complexes.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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