## Abstract The polymerization kinetics of methyl methacrylate (MMA) was studied, using Tl(III)βcyclohexanone (CH) redox system as initiator, in the presence of emulsifier [i.e., sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB), and thallium triacetate (TXβ100)] over a temperatur
Polymerization mechanisms and molecular weight distributions. III. Gamma-radiation-initiated polymerization of methyl methacrylate
β Scribed by Jorma G. Braks; Gunter Mayer; Robert Y. M. Huang
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 339 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Abstract
The termination mechanism in gammaβradiationβinitiated polymerization of methyl methacrylate was investigated. The termination mechanism and the associated rate constants were determined by comparing the theoretical molecular weight distribution (MWD) and the experimental MWD, which was determined by gel permeation chromatography. Disproportionation occurs 1.2 times as frequently as combination at 30Β°C and 0.5 times as frequently at 0Β°C. The activation energy for disproportionation is 5.5 kcal/mole greater than that for combination. The rates of initiation were determined by a new method and were found to compare well with those reported in the literature. It is also suggested that it is necessary for the theoretical MWD to have the same shape as the experimental MWD before a mechanism can be authenticated.
π SIMILAR VOLUMES
Using a radiation peroxide grafting technique, a ultrahigh molecular weight polyethylene (UHMWPE) stored at room temperature for 10 days after irradiation in air was graft copolymerized with methyl methacrylate (MMA) in the presence of metallic salt and acid. The MMA-grafted UHMWPE samples were anal