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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 18 (1985), S. 1310-1314 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 60 (1977), S. 49-86 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Morphologie heterogener Polymermischungen aus Polybutadien (PBD) und Äthylen-Propylen-Dien-Terpolymeren (EPDM) wurde selektiv variiert, indem entweder die Rheologie der Mischungskomponenten während der Mischung oder die Zusammensetzung der Mischung geändert wurden. Bei gegebenen Mischungsbedingungen nähert sich das Mischungssystem einer „Steady-State-Morphologie“, die sich als relativ unabhängig von der Vorgeschichte der Probe erwies. Bei nachfolgender Formgebung kann sich jedoch die Morphologie wesentlich ändern, wobei in einigen Fällen Phasenumwandlung eintritt. Für das rheologisch-morphologische Verhalten wird ein Mechanismus vorgeschlagen.Die Dehnungsmoduln der durch Bestrahlung der Elastomermischungen hergestellten Vulkanisate glichen denjenigen, die durch die Takayanagi-Modelle vorausgesagt wurden. Ein positiver Synergismus hinsichtlich der Bruchenergie und der Zugspannung beim Bruch wurde speziell in den Fällen beobachtet, in denen die Mischungskoponenten ein ausgesprochen unterschiedliches mechanisches Verhalten zeigten. Die Empfindlichkeit des Zug-Dehnungsverhaltens dieser Mischungen bezüglich der änderungen in der Morphologie erwies sich geringer als vorher angenommen. Dies wird auf Einschränkungen in der Bewegungsmöglichkeit der weicheren durch die harte Phase in der Mischung zurückgeführt.
    Notes: The morphology of heterogeneous blends of polybutadiene (PBD) and EPDM was selectively varied by a change of either the rheology of the blend components during mixing or of the blend composition. Under a given set of mixing conditions, the blend system approaches a “steady state morphology”, which was found to be relatively independent of sample history. However, during subsequent compression molding, the morphology of the sample may be altered substantially with phase inversion occurring in some cases. A mechanism is proposed for the observed rheology-morphology behavior.The strain moduli of the vulcanizates prepared by irradiation of the elastomer blends were similar to those predicted using the parallel Takayanagi models. A positive synergism with respect to energy to break and stress at break was noted particularly in cases where the blend components showed a significantly different mechanical response. The sensitivity of the stress-strain response of these blends to changes in morphology was less than anticipated. This is attributed to restrictions imposed on the movement of the softer phase by the hard phase component of the blend.
    Additional Material: 19 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 30 (1985), S. 2021-2030 
    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: It is demonstrated that the improved tack and green strength accompanying the IAD modification of polybutadiene arise strictly from the introduction of bulky, polar groups. The fact that addition of 1,4-PB occurs in a blocked arrangement is not a factor in the development of high green strength, as can be seen by the large increase in strength of modified 1,2-PB, wherein the IAD groups are randomly attached. The tack is also elevated through random IAD addition; however, the relevance of blocked vs. random structure in this regard cannot be completely judged since it depends as well on the absolute IAD level and the polymer's Tg, as well as the test temperature. At high levels of IAD (about 38 mol %), the modified PB becomes a phase-separated material, exhibiting high stiffness and brittleness. This heterogeneous system is quite unlike the PB modified with only 15 mol % IAD. These latter elastomeric materials are homogenous, and remain so during deformation. The attainment of high tack and green strength relies upon maximal addition of the IAD groups, provided the molecules retain their flexibility. In blending the modified PB with other rubbers, optimum behavior in the blends appears to be achieved when the IAD-PB is present as a continuous phase.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 3193-3209 
    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 physical properties of radiation- and sulfur-cured poly(butadiene-co-styrene)-based stocks were compared. It was found that the measured lower ultimate strength of radiation-cured stocks is in part attributable to the difference in the glass transition temperatures of the stocks cured by the two methods (an increase in Tg is caused by sulfur curing). Another factor contributing to the difference in performance is the apparent nonuniform crosslink density distribution in radiationcured stocks containing carbon black filler. A higher crosslink density in the immediate vicinity of carbon black particles was postulated based on a to-be-expected distribution of secondary electron energy at interfaces with an appreciable change in density between neighboring phases. The invoked difference in network topology, supported by solvent swelling measurements on sulfur- and radiation-crosslinked vulcanizates can explain not only the slightly lower ultimate strength of radiation-cured stocks but also the superior fatigue and crack propagation performance measured for these culcanizates. Finally, theoretical arguments were presented to explain the inferred large strength deficiency of radiation-cured rubbers reported by other investigators on the basis of chain scissions encountered during radiation crosslinking.
    Additional Material: 13 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 29 (1984), S. 3803-3812 
    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 addition of IAD pendant groups to PB molecules results in a larger effective chain crosssectional area with consequent decrease in chain entanglements. This causes the rubber to be more complaint at low strains and strain rates. Simultaneously, the IAD structures give rise to polar and H-bond interactions which cause the material to exhibit strong adhesion and to possess high green strength. As a result, the IAD-PB is a relatively rare example of a synthetic polymer with good autoadhesive properties.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 7 (1969), S. 535-539 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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