High-pressure ethylene polymerization initiated by peroxide
✍ Scribed by Kodama, Shinjiro ;Shimidzu, Takeo ;Yuasa, Sachio ;Kagiya, Tsutomu ;Fukui, Kenichi
- Publisher
- John Wiley and Sons
- Year
- 1961
- Weight
- 483 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0022-3832
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✦ Synopsis
Abstract
The polymerization of ethylene initiated by di‐tert‐butyl peroxide is studied in batch system under pressures ranging from 300 to 1700 kg./cm.^2^, and at temperatures of 110 to 170°C., using reaction mediums of water, ethyl alcohol, and their mixture. An experimental rate equation in water is:
The rate is proportional to the concentration of radical produced by the first‐order decomposition of initiator. A reaction scheme is proposed from which this rate equation can be derived. According to this scheme, the deactivation of radical is kinetically of the first order with respect to the radical concentration. Several relations between the reaction conditions and properties of polyethylene produced are also described.
📜 SIMILAR VOLUMES
## Abstract A kinetic model of a high‐pressure, free‐radical ethylene polymerization is presented. The model of S. Goto, K. Yamamoto, S. Furui, and M. Sugimoto (J Appl Polym Sci, Appl Polym Symp 1981, 36, 21), developed for several common peroxides, was extended to be applicable for the oxygen init
## Abstract Ethylene polymerization can be carried out under milder conditions than heretofore because of the development of peroxydicarbonate catalysts. This simplifies study of polymerization kinetics. Diethyl peroxydicarbonate undergoes first‐order decomposition in __tert__‐butyl alcohol with an