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ABSTRACT:The kinetics of glycidyl methacrylate block polymerization to high conversion was experimentally investigated with variations of the photoinitiator concentration, temperature, and power of UV illumination. The kinetic curves of this polymerization process contain three characterized sections of coordinates of "conversion-time," namely: The first one is practically linear to a conversion of Ϸ0.5, the second represents, by itself, the autoacceleration process, and the third presents the autodecelation process. An additional peculiarity of such a polymerization process is poor reproduction of the kinetic measurements. This reproduction does not correspond to instrumental error. Derivation of a kinetic model for block linear polymerization was done. This model is, quantitatively, in good agreement with all the data of the experimental material.

ABSTRACT:The kinetics of postpolymerization (after ultraviolet illumination was stopped) for a number of dimethacrylates that differed by nature and molecular mass was experimentally studied over a wide range of temperatures. A series of kinetic curves that differed by the starting conversion of the dark period of time was obtained for every temperature. The proposed kinetic model of the process is based on the following main principles: (1) the process at an interface on the liquid monomer-solid polymer (micrograins) boundary takes a main share of the kinetics of postpolymerization; (2) chain termination at an interface is monomolecular, is controlled by the chain propagation rate, and represents by itself the self-burial act of active radicals in the conformation trap; and (3) monomolecular chain termination is characterized by a wide spectrum of characteristic times and that is why the function of the relaxation is described by Kohlrausch's stretched exponential law. The obtained kinetic equation was in good agreement with all of the sets of experimental data. This permitted us to estimate the rate constant of chain termination (k t ) and to determine the scaling dependence of k t on the molar-volumetric concentration of the monomer in bulk [M 0 ]. We assumed that the stretched exponential law and scaling dependence k t from [M 0 ] were characterized by common peculiarities, namely, a wide range of characteristic times of relaxation possessed by a property of the fractal set.

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