Emulsion polymerization of ethylene. V. Kinetics and mechanism
β Scribed by H. K. Stryker; G. J. Mantell; A. F. Helin
- Publisher
- John Wiley and Sons
- Year
- 1967
- Tongue
- English
- Weight
- 1004 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
The solubility of ethylene was measured in water, water-tert-butyl alcohol, wateremulsifier, water-tert-butyl alcohol-emulsifier, and water-tert-bntyl alcohol-emulsifierpolyethylene. The polymerization of ethylene in an emulsion system differs from that of other vinyl monomers in several ways: the rate of polymer formation is inversely proportional to the emulsifier concentration and to the number of particles, the molecular weight of the polymer increases as the particle size increases, the polymer contains bound emulsifier whose concentration depends inversely ou the particle diameter. These peculiarities are attributed to a transfer reaction between polymer radicals and emulsifier adsorbed on the surface of the polymer particle. In the preseuce of a fatty-acid soap, the transfer probably occurs primarily at the carbon LY to the carboxyl group.
π SIMILAR VOLUMES
Kinetics of ethylene homopolymerization reactions and ethylene/1-hexene copolymerization reactions using a supported Ziegler-Natta catalyst was carried out over a broad range of reaction conditions. The kinetic data were analyzed using a concept of multicenter catalysis with different centers that r
Kinetics and mechanism of the emulsion polymerization of vinyl acetate by redox initiation ## 2. L.cperittwnlrt1 'l'lie experimental riiethods crnployt:tl wen: itlentical with ttiosc described previously [17, IS]. The image analyzer (Biltlanalyse IBAS 1 arid 3) was used to measure t h e average d