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Polymer formation induction time

For the case of acrylonitrile, there was an induction time of 24 h. This was attributed to the formation of cyanide radicals which are able to react with polyamidic macroradicals. The interpolymer is composed of two fractions one soluble in dimethyl formamide, whose properties are similar to polyacrylonitrile the other, insoluble in this solvent, whose properties are similar to those of the polyamide. No homopolymer was observed. The presence of acrylonitrile on the graft polymer was demonstrated by IR. [Pg.19]

The induction period is defined as the time elapsed from the initial mixing and heating of the reaction mixture until the initial polymer formation... [Pg.72]

Inhibition of spontaneous polymerization of (meth) acrylates is necessary not only at their storage but also in the conditions of their synthesis proceeding in the presence of sulfuric acid. In this case, monomer stabilization is more urgent, since sulfuric acid not only deactivates mat r inhibitors but also is capable of intensifying polymer formation. The concentration dependence of induction periods in these conditions has a brightly expressed nonlinear character. And, unlike polymerization in bulk, decomposition of polymeric peroxides is observed at relatively low temperatures in the presence of sulfuric acid, and the values [X] of the amines studied are by ca. 10 times lower than [HQ]. ... [Pg.88]

Isothermal crystallization of a polymer is frequently characterized by the induction time and the crystallization half-time. The crystallization induction time is the time that elapses from the moment when the desired crystallization temperature is reached to the onset of crystallization, characterized by the formation of the first nuclei. The crystallization half-time is the time when relative crystallinity reaches 0.5. More detailed analyses of the isothermal crystallization are usually based on the Avrami-Evans theory. Equation (7.10) yields ... [Pg.230]

Fig. 2.3.4 Film formation of a photoinitiated the lower surface (left) after a 90 min induction cross-linking latex coating as measured by period due to oxygen absorption. The profiles CARField. (a) The coating is exposed to air shown were recorded 10, 90, 100 and 110 min (evaporation) and light from above, (b) A sam- and 2, 3, 4, 5, 6 and 17 h after casting the layer, pie comprising a combination of only polymer (d)The full formulation film forms in the central and water dries from the upper surface (right) layers first. In this final time series, the profiles as shown by a time series of profiles, recorded shown were recorded after 10 min (dotted at 10, 20, 30, 40, 50, 60, 70, 100 and 120 min trace, T) attenuated) and then, from the top after casting the layer, (c) A combination of down, 30, 60 and 90 min and 2, 3, 6 and 17 h polymer and photoinitiator only cures from after casting the layer. Fig. 2.3.4 Film formation of a photoinitiated the lower surface (left) after a 90 min induction cross-linking latex coating as measured by period due to oxygen absorption. The profiles CARField. (a) The coating is exposed to air shown were recorded 10, 90, 100 and 110 min (evaporation) and light from above, (b) A sam- and 2, 3, 4, 5, 6 and 17 h after casting the layer, pie comprising a combination of only polymer (d)The full formulation film forms in the central and water dries from the upper surface (right) layers first. In this final time series, the profiles as shown by a time series of profiles, recorded shown were recorded after 10 min (dotted at 10, 20, 30, 40, 50, 60, 70, 100 and 120 min trace, T) attenuated) and then, from the top after casting the layer, (c) A combination of down, 30, 60 and 90 min and 2, 3, 6 and 17 h polymer and photoinitiator only cures from after casting the layer.

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See also in sourсe #XX -- [ Pg.166 ]




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