NIPPON GOMU KYOKAISHI
Print ISSN : 0029-022X
Volume 59, Issue 10
Displaying 1-8 of 8 articles from this issue
  • [in Japanese]
    1986 Volume 59 Issue 10 Pages 545-551
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL FREE ACCESS
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  • [in Japanese]
    1986 Volume 59 Issue 10 Pages 552-554
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL FREE ACCESS
    Download PDF (447K)
  • [in Japanese], [in Japanese]
    1986 Volume 59 Issue 10 Pages 555-564
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL FREE ACCESS
    Download PDF (1254K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    1986 Volume 59 Issue 10 Pages 565-567
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL FREE ACCESS
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  • Taiji MIYAKE, Shuuji MORIUCHI, Yoshihiro MASUDA, Fumikazu YAMAGATA
    1986 Volume 59 Issue 10 Pages 568-573
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL FREE ACCESS
    The mechanism for crosslinking of various EPDM rubbers has not yet been clearly established, though the mechanism is assumed to be based on the recombination of two polymer radicals produced by the extraction of hydrogen from activated methylene, methyne or methyl groups neibouring the olefinic double bond in EPDM molecules. This study was intended to elucidate the crosslinking mechanism of three tyeps of EPDM, i. e., dicyclopentadiene, ethylidene norbornene, and 1, 4-hexadiene types by using an electron spin resonance spectrometer. The experimental procedure was based on the so-called spin trapping method by using 2, 4, 6-tri-tertbutylnitrosobenzene as a radical trapping agent and benzoyl peroxide as a radical initiator for EPDM in n-heptane solution to afford the molecular structure of polymer radicals. This study enables us to elucidate the moleculer structure of the crosslinking point. The difference hed seen the cure rates of the three types of EPDM was referred from the results.
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  • Study on Structual Changes Caused by Fatigue Due to Three-Dimensional Stresses
    Kunihiko FUJIMOTO, Naoto MIFUNE, Haruhisa KOFUJI, Tadahiro UEKI
    1986 Volume 59 Issue 10 Pages 574-583
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL FREE ACCESS
    We investigated structual changes in rubber molecular chain phases and in carbon black aggregated phases in carbon black filled NR vulcanizates, casued by fatigue due to three-dimensional stresses developed by round projections, by measuring the mobility of rubber molecule, amount of weak physical bonds, thermodynamic properties of modulus and dispersed structure of carbon black particules. We inferred that the rubber molecular chain phases of high mobility (A phase) and rubber molecular chain phases of low mobility (C phase) come to form different thermodynamic structures, thereby producing a heterogeneous structure of the system. And carbon black aggregates structures are oriented in the direction of principal tensile stress, forming layers of about 0.5μm at regular intervals in the direction of principal compression stresses. Meanwhile, structures of rubber molecules within a layer are oriented in the direction of a layer and rubber molecules between layers come to form random structures of increased free volume.
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  • Study on Temperature Dependences of Dynamic Properties of Rubber Vulcanizates Fatigued with Three-Dimensional Stresses
    Kunihiko FUJIMOTO, Naoto MIFUNE
    1986 Volume 59 Issue 10 Pages 584-589
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL FREE ACCESS
    In the previous paper, it was inferred that rubber molecular chain phases and carbon black aggregated phases form the anisotropic layer structure on account of fatigue due to three-dimensional stresses. Along the direction of tensile stresses, rubber molecular chain phases within the layer are oriented and in consequence they acquire low mobilities, whereas along the direction of compression stresses, rubber molecular chain phases between layers form random structures and they acquire high mobilities.
    In this paper is investigated in detail the influence of the anisotropic layer structure on the mobilities of rubber molecular chains by measuring the dependence of the dynamic properties on temperature. Temperatures, exhibiting maxmal tan δ, shift to high temperature side along the parallel direction of layer and to low temperature side along the perpendicular direction of layer. Thus it is seen that rubber molecular chain phases have low mobilities and high mobilities along different directions.
    Consequently, it is confirmed that the rubber molecular chain phases form oriented structures within a single layer and random structures between different layers.
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  • [in Japanese]
    1986 Volume 59 Issue 10 Pages 590-591
    Published: 1986
    Released on J-STAGE: July 09, 2007
    JOURNAL RESTRICTED ACCESS
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