Emulsion polymerization of vinyl acetate
β Scribed by Okamura, Seizo ;Motoyama, Takuhiko
- Book ID
- 104532137
- Publisher
- John Wiley and Sons
- Year
- 1962
- Weight
- 394 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0022-3832
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β¦ Synopsis
Abstract
It is generally admitted that the SmithβEwart equation is not applicable to the emulsion polymerization of vinyl acetate. This is considered to be due to two factors, namely, (1) the great solubility in water of vinyl acetate and (2) the fact that vinyl acetate is easily subject to the influences of retarders or chain transfer agents. However, examination of the polymerization of vinyl caproate and of styrene leads to the conclusion that the special features pertaining to the polymerization of vinyl acetate are to be attributed to its solubility in water. The reason is that vinyl caproate, which is less soluble in water but subject to the influences of retarders or chain transfer agents in the same degree as vinyl acetate, follows the SmithβEwart equation in emulsion polymerization, and styrene, when polymerized in aqueous methanol, in which the solubility of styrene increases, shows a diminished SmithβEwart exponent.
π SIMILAR VOLUMES
Studies have been made of the 7-induced emulsion polymerization of styrene and comparisons made with chemically initiated emulsion polymerization. The polymerization proceeded smoothly to high conversions at 0 and 60Β°C, the reaction showing a high G (monomer) value. Complete conversions were obtaine
The emulsion polymerization of vinyl acetate was studied a t 50Β°C. 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