The emulsion polymerization of vinyl acetate was studied a t 50ยฐC. It was found that the rate of polymerization was proportional to the 0.5 power of the initiator concentration and the 0.25 power of the number of particles. The number of particles was proportional to the power 0.5 f 0.05 of the emul
A kinetic study of vinyl acetate polymerization in aqueous media in the absence of emulsifier
โ Scribed by M. Nomura; S. Sasaki; M. Harada; W. Eguchi
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 862 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
In the absence of emulsifying agents, vinyl acetate polymerization in aqueous media was carried out at 50ยฐC over a wide range of initial initiator and monomer concentrations to clarify the effect of reaction conditions on the kinetic behavior of the polymerization system. It was shown that the rate of polymerization was proportional to reaction time and initiator concentration and independent of the number of polymer particles present. The rate could also be successfully explained by the Smith and Ewart theory for emulsion polymerization when the dissolved monomer in water and the Trommsdorff effect were taken into consideration. A set of equations which could account for the effect of dissolved monomer in water on the rate of polymerization is proposed.
๐ SIMILAR VOLUMES
The free-radical polymerization behavior of 1-vinyl,2-pyrrolidone (NVP) was studied at low conversions, using capillary dilatometry. The aqueous media were kept at neutral pH and the studies were conducted isothermally, at 40 or 45ยฐC. The azo-type initiators used were 4,4ะ-azobis-4-cyanopentanoic ac