ln order to adapt the reduction-activation reaction of hydrogen peroxide to the polymerization of 2-phenyl-l,3-butadiene, emulsion polymerization was carried out with H202/Fe 2+ as catalyst in the presence of sodium pyrophosphate. The influences of emulsifier, iron ligand, electrolyte salt and polym
The emulsion polymerization of 2,3-dimethylbutadiene-1,3
β Scribed by Morton, Maurice ;Gibbs, William E.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1963
- Tongue
- English
- Weight
- 899 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0449-2951
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β¦ Synopsis
Abstract
A study has been carried out on the kinetics of the emulsion polymerization of 2,3βdimethylbutadieneβ1,3. The kinetic treatment of Smith and Ewart was applied for the direct determination of the absolute propagation rate constant k~p~. The following expression was obtained: k~p~ = 8.9 Γ 10^7^ exp {β9000/RT} liter/mole/sec. A previously developed treatment was applied to the determination of the relative and absolute crosslinking rates of 2,3βdimethylbutadieneβ1,3. The results led to the following expression for the absolute crosslinking rate constant k~x~: k~x~ = 3.0 Γ 10^6^ exp {β14400/RT} liter/mole/sec. A comparison of these rate constants was made for the three dienes, viz., butadiene, isoprene, and dimethylbutadiene. The propagation rate constants were found to vary only by a factor of 2β3. However, the crosslinking rates were found to decrease considerably in going from butadiene to isoprene to dimethylbutadiene. This was attributed, mainly, to the decreased sideβvinyl content of the latter two monomers, compared to butadiene, as well as to the steric hindrance imposed by the presence of the methyl group.
π SIMILAR VOLUMES
Homopolymerizations of butadiene (BD), isoprene (IP), and 2,3-dimethylbutadiene (DMBD) were carried out by a Gd(OCOCCl 3 ) 3 -based catalyst, to investigate the effects of the energy levels of the monomers or the sterical factor of the methyl substituents on the polymerizability and the cis-selectiv
The vibrational structure of the 3pr Rpdbcrg transition of 2.3-dimethplbutadienc has been recorded and analyzed. A signifknt reduction in frequency of the lower -CHs torsion on excitation is observed in bo?h this state and in the 4fI and 4f2 Rfdbee states.