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Studies in radiation-induced polymerization of vinyl monomers at high dose rates. II. Methyl methacrylate

โœ Scribed by C. C. Allen; W. Oraby; T. M. A. Hossain; E. P. Stahel; D. R. Squire; V. T. Stannett


Publisher
John Wiley and Sons
Year
1974
Tongue
English
Weight
770 KB
Volume
18
Category
Article
ISSN
0021-8995

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โœฆ Synopsis


The radiation-induced polymerization of methyl methacrylate was investigated with radiation sources of cobalt 60 and accelerated electrons at dose rates up to 3 Mrads/ sec. Extrapolation of previous rates of polymerization at. dose rates of 0.01-200 rads/sec coincided with the present results, the rates being approximately proportional to the square root of the dose rate throughout the entire set of dose rates measured. The molecular weights seemed to be independent of dose rate at the highest dose rates investigated. A combination of high polymer with a much higher molecular weight than expected was formed, together with a substantial portion of low molecular weight polymer.

The reason for this behavior is not clear at this time. The G ( M . ) calculated from the molecular weights and fraction of polymer and resin was 6.0, which approaches that, reported in previous investigations a t low dose rates. There was no significant effect of air on the polymerization kinetics of methyl methacrylate a t above 1 Mrad/sec. Nitrogen also did not influence the measured rates. Conversions to polymer were not sub- stantially reduced by the presence of inhibitor at above 1.26 X lo5 rads/sec. Water did not influence the rates of polymerization, except a t the highest temperature (50ยฐC) investigated. A large posteffect was observed in sealed degassed ampoules after 25% conversion to polymer. Only 3.4y0 additional polymer was formed in 24 hr after irradiation in the presence of air. The activation energy for the electron beam polymerization of methyl methacrylate was about 7.0 kcal/mole. This value, considering the complications in technique such as beam heating, did not differ from literature data enough to suggest any mechanistic difference in the polymerization at high dose rates.


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