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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 709-725 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: 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 at low dose rates. There was no significant effect of air on the polymerization kinetics of methyl methacrylate at above 1 Mrad/sec. Nitrogen also did not influence the measured rates. Conversions to polymer were not substantially reduced by the presence of inhibitor at above 1.26 × 105 rads/sec. Water did not influence the rates of polymerization, except at the highest temperature (50°C) investigated. A large posteffect was observed in sealed degassed ampoules after 25% conversion to polymer. Only 3.4% 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.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 6 (1968), S. 1-25 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of biopolymerization on nucleic acid templates is discussed. The model introduced allows for the simultaneous synthesis of several chains, of a given type, on a common template, e.g., the polyribosome situation. Each growth center [growing chain end plus enzyme(s)] moves one template site at a time, but blocks L adjacent sites. Solutions are found for the probability nj(t) that a template has a growing center that occupies the sites j  -  L + 1,…, j at time t. Two special sets of solutions are considered, the uniform-density solutions, for which nj(t) = n, and the more general steady-state solutions, for which dnj(t)/dt = 0. In the uniform-density case, there is an upper bound to the range of rates of polymerization that can occur. Corresponding to this maximum rate, there is one uniform solution. For a polymerization rate less than this maximum, there are two uniform solutions that give the same rate. In the steady-state case, only L = 1 is discussed. For a steady-state polymerization rate less than the maximum uniform-density rate, the steady-state solutions consist of either one or two regions of nearly uniform density, with the density value(s) assumed in the uniform region(s) being either or both of the uniform-density solutions corresponding to that polymerization rate. For a steady-state polymerization rate equal to or slightly larger than the maximum uniform-density rate, the steady-state solutions are nearly uniform to the single uniform-density solution for the maximum rate. The boundary conditions (rate of initiation and rate, of release of completed chains from the template) govern the choice among the possible solutions, i.e., determine the region(s) of uniformity and the value(s) assumed in the uniform region(s).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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