Rate Constant of Initiation Reaction in Cationic Polymerization of Vinyl Monomers. I. Polymerization of Styrene Derivatives Catalyzed by Triphenylmethyl Stannic Pentachloride

1967 ◽  
Vol 1 (4) ◽  
pp. 683-697 ◽  
Author(s):  
T. Higashimura ◽  
T. Fukushima ◽  
S. Okamura

1987 ◽  
Vol 18 (2) ◽  
Author(s):  
Toshinobu Higashimura ◽  
Yasuhisa Kishimoto ◽  
Sadahito Aoshima


2020 ◽  
Vol 11 (42) ◽  
pp. 6739-6744
Author(s):  
Koji Takagi ◽  
Hiroto Murakata ◽  
Koji Yamauchi ◽  
Kohei Hashimoto

Cationic polymerization of vinyl monomers was investigated using non-ionic and ionic halogen bonding organocatalysts.



1992 ◽  
Vol 30 (7) ◽  
pp. 1495-1498 ◽  
Author(s):  
Ichiro Atobe ◽  
Toshikazu Takata ◽  
Takeshi Endo






1975 ◽  
Vol 53 (18) ◽  
pp. 2742-2747 ◽  
Author(s):  
Philip D. Pacey

Dimethyl ether was pyrolized in a flow system at 782–936 K and 25–395 Torr with conversions from 0.2–10%. Product analyses were consistent with a simple Rice–Herzfeld mechanism with most chain termination by the recombination of CH3 radicals. The rate coefficients for both the initiation and termination reactions appeared to be slightly pressure dependent. The first-order rate constant for the initiation reaction,[Formula: see text]calculated from the rate of C2H6 formation, was k1 = 1015.0±0.5exp (−318 ± 8 kJ mol−1/RT) s−1, corresponding to ΔHf0(CH3O) = −5 ± 8 kJmol−1. Comparison of CH4 and C2H6 yields enabled calculation of the rate constant for the reaction of CH3 with dimethyl ether. From 373−936 K, the Arrhenius plot for this reaction is a curve.



1969 ◽  
Vol 26 (289) ◽  
pp. 369-373 ◽  
Author(s):  
Kohtaro Ikeda ◽  
Toshinobu Higashimura ◽  
Seizo Okamura


Kobunshi ◽  
1989 ◽  
Vol 38 (11) ◽  
pp. 1018-1021
Author(s):  
Mitsuo Sawamoto


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