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  • cationic polymerization  (2)
  • Ethylene-propylene copolymers  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 259 (1981), S. 1190-1197 
    ISSN: 1435-1536
    Keywords: Ethylene-propylene copolymers ; crosslinking ; irradiation ; rheo-optical properties ; crystallinity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary The rheooptical behaviour of radiation crosslinked networks of four commercial ethylene-propylene (E-P) copolymers having different molecular masses and propylene contents from 20 to 35 mol. % was investigated in the main transition and rubbery regions.C p(T) of E-P copolymers prior to irradiation was determined in the range 240–370 K, and the degree of crystallinity was estimated. Crystallinity considerably affected the viscoelastic (mechanical, and particularly optical) behaviour of the networks with a lower propylene content (≈ 20 mol %) in the temperature range 120–338 K. Due to a form contribution of the crystallites to the birefringence, the stress-optical function exhibits a pronounced maximum depending on temperature and time connected with melting of the crystalline phase. In the rubbery region (T 〉 340 K) the dependence of the Mooney-Rivlin constantC 1 on the radiation doseD was the same for all series of networks; the composition of E-P copolymers and especially their molecular masses were reflected in the value of theC 2 parameter and in its dependence onD. Deep in the rubbery region, lightly crosslinked networks exhibited pronounced time dependences of mechanical and optical functions. The high values of extrapolated equilibrium parametersC 1 andC 2 e suggest an important contribution of trapped entanglements to the equilibrium modulus.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 651-663 
    ISSN: 0887-624X
    Keywords: cationic polymerization ; epoxide network ; theory of network formation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Network formation in cationic polymerization of polyepoxides was treated using a combination of kinetic theory and the statistical theory of branching processes (TBP). The complex reaction mechanism involved a degradative termination reaction affecting the molecular weight distribution of the primary chains. Moreover, formation of low-molecular-weight products, initiation, two mechanisms of propagation and transfer were taken into account. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 651-663, 1997
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 665-672 
    ISSN: 0887-624X
    Keywords: cationic polymerization ; epoxide network ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The theory of network formation developed for the cationic polymerization of diglycidyl ether of Bisphenol A was modified for the presence of a reactive diluent γ-butyrolactone and tested by comparison with experimental results. It was shown that the theory predicts quite reasonably the structure evolution during polymerization characterized by growth of the polymer fraction, gelation, increase in gel fraction, as well as the equilibrium rubber modulus of cured samples. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 665-672, 1997
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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