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  • Polymer and Materials Science  (2)
  • 1965-1969  (2)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 1053-1074 
    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 model polyurethanes and polyureas, a polyamide, and a polyimide were prepared by reacting 4,4′-diphenylmethane diisocyanate or polyisocyanates having similar polybenzyl structures with aliphatic or aromatic coreactants. Thermogravimetric analyses indicated that the flammability of the polymers was related to the formation of volatile flammable products during early stages of decomposition. Determinations of the heat evolved during differential thermal analyses and of the thermodynamic heats of combustion suggested that the extent and rate of reaction were among the important factors governing flame propagation. Flame-resistant polymers were prepared by use of structural elements which were thermally stable and nonvolatile or which formed nonflammable decomposition products.
    Additional Material: 12 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 13 (1969), S. 1277-1288 
    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 development of new and more sensitive techniques in thermal analyses aids in a more complete understanding of the contributions of individual components in urethane elastomers regarding their mechanical and thermodynamic behavior. The behavior of various segments of the elastomers reported in this work illustrates a clearer interpretation of reasons for changes in mechanical behavior caused by changes in heat capacity, volume and tensile properties; the gross changes previously reported for polyurethane properties as a function of temperature are also confirmed with a more exact definition of their origin.The sub-ambient temperature behavior and response of physical measurements near the melting point of the backbone polyol are largely a function of the so-called “soft block.” The soft block does not contribute to the mechanical properties above the melting point of the polyol unless some urethane segments from the diisocyanate and extender are structured into the soft block, that is, excess diisocyanate and extender are added to build in the “hard” block. The extender and isocyanate influence for both low and high temperature properties is observed by the lack of molecular fit imparted to the backbone polyol as well as some crystallinity in the polymer hard block. The usual Tg transition reported in urethane elastomers corresponds to a first-order transition in the polyester or polyether backbone.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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