Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Akinori Kameyama"'
Autor:
Yoshihiro Takayama, Akira Matsumoto, Hirofumi Yamasaki, Hiroyuki Aota, Tsuneo Nakanishi, Akinori Kameyama, Masahiro Katsumoto
Publikováno v:
European Polymer Journal. 36:1741-1744
Triallyl isocyanurate (TAIC), a bulky monomer, was copolymerized radically with sterically unhindered monomers including 1-octene (Oc), vinyl caproate (VCa) and vinyl laurate (VLa). Fineman–Ross plots to evaluate the monomer reactivity ratios showe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fbb6fd56ee77b7edf46f9ffc49918d0
https://doi.org/10.1016/s0014-3057(99)00224-4
https://doi.org/10.1016/s0014-3057(99)00224-4
Autor:
Tsuneo Nakanishi, Yoshihiro Takayama, Hiroyuki Aota, Akinori Kameyama, Akira Matsumoto, Katsuyuki Watanabe
Publikováno v:
Polymer. 41:3883-3886
Cyclopolymerization of triallyl isocyanurate (TAIC) as compared with its isomer triallyl cyanurate (TAC) is discussed in terms of the nonterminal units effect caused by the sterically bulky isocyanurate side groups. Thus, the monomer concentration de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c8a949b3c6e5cca913debd49883d740
https://doi.org/10.1016/s0032-3861(99)00676-x
https://doi.org/10.1016/s0032-3861(99)00676-x
Autor:
Tsuneo Nakanishi, Tsuyoshi Kubo, Yoshihiro Takayama, Hiroyuki Aota, Akira Matsumoto, Akinori Kameyama, Katsuyuki Watanabe
Publikováno v:
European Polymer Journal. 36:673-677
The temperature effect on the polymerization of triallyl isocyanurate (TAIC) was explored in detail as compared with its isomer triallyl cyanurate (TAC), since TAIC and TAC are commercially important as crosslinking agents with comonomers, and for af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e73b1bd1221d0313fbc09e63f4cac47
https://doi.org/10.1016/s0014-3057(99)00129-9
https://doi.org/10.1016/s0014-3057(99)00129-9
Autor:
Tsuneo Nakanishi, Yoshinari Sumiyama, Yoshihiro Takayama, Hiroyuki Aota, Akinori Kameyama, Akira Matsumoto
Publikováno v:
Journal of Macromolecular Science, Part A. 36:1537-1545
Radical solution polymerization of triallyl isocyanurate was conducted in methyl benzoate or hexyl benzoate as good or poor solvent, respectively, using AIBN as initiator at 60°C. An increased rate of polymerization, enlarged primary chain length, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0346c61458357ee88a4ab2723ca562b5
https://doi.org/10.1081/ma-100101613
https://doi.org/10.1081/ma-100101613
Autor:
Akinori Kameyama, Tsuyoshi Kubo, Akira Matsumoto, Hiroyuki Aota, Tsuneo Nakanishi, Yoshihiro Takayama, Toru Yamakawa
Publikováno v:
Die Angewandte Makromolekulare Chemie. 268:36-40
It is not possible to improve the toughness of triallyl isocyanurate (TAIC) resins by applying the procedures useful for diallyl phthalate (DAP) resins as typical allyl resins. The results obtained are discussed in connection with the network structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b84674cd3a06ee7d7e5e745bfa2b2a2
https://doi.org/10.1002/(sici)1522-9505(19990701)268:1<36::aid-apmc36>3.0.co
https://doi.org/10.1002/(sici)1522-9505(19990701)268:1<36::aid-apmc36>3.0.co
Autor:
Akinori Kameyama, Fuminori Hirai, Yoshinari Sumiyama, Hiroyuki Aota, Akira Matsumoto, Tsuneo Nakanishi, Yoshihiro Takayama
Publikováno v:
European Polymer Journal. 35:195-199
As part of our continuing studies concerned with the radical polymerization of multiallyl compounds, the polymerization behavior of triallyl isocyanurate (TAIC) was compared in detail with those of its isomer triallyl cyanurate (TAC). It was found by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37d35ac1c040fc8df54b7cbcd329c1ec
https://doi.org/10.1016/s0014-3057(98)00131-1
https://doi.org/10.1016/s0014-3057(98)00131-1
Autor:
Tsukasa Matsumoto, Mikio Hirabayashi, Tsuneo Nakanishi, Akinori Kameyama, Katsuyuki Watanabe, Akira Matsumoto, Hiroyuki Aota
Publikováno v:
Journal of Macromolecular Science, Part A. 35:1889-1893
Polymerizations of several diallyl alkyl isocyanurates were investigated to explore in more detail the steric effect observed in the polymerization of triallyl isocyanurate [3, 5], as compared to its isomer triallyl cyanurate, by changing alkyl group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e77eec22889a5bb9a3ab6674ebdd29
https://doi.org/10.1080/10601329808000559
https://doi.org/10.1080/10601329808000559
Autor:
Akinori Kameyama, Kazuyoshi Nishizawa, Yoshihiro Takayama, Tsuneo Nakanishi, Hiroyuki Aota, Daisuke Ishihara, Akira Matsumoto
Publikováno v:
Polymer Journal. 32:79-81
Specific Polymerization Behavior of Triallyl Isocyanurate. Accumulation of Radicals before Gelation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b44aba5f89e82f6421dc728e3b9464f
https://doi.org/10.1295/polymj.32.79
https://doi.org/10.1295/polymj.32.79