Room temperature‐initiated and self‐heating copolymerization of acrylonitrile with vinyl acetate

Abstract

A novel polymerization method [Ruckenstein and Li, Polymer Bull., 37, 43 (1996)]—room temperature-initiated, self-heating polymerization—was applied to both bulk and concentrated emulsion copolymerization of acrylonitrile (AN) with vinyl acetate (VAc). A redox system was employed as an initiator, with the oxidant dissolved in the monomers and the reductants (two reductants were employed) in the aqueous phase. In the bulk polymerization, the oxidant (cumene hydroperoxide) was dissolved in the mixture of monomers, and the two reductants (sodium metabisulfite and ferrous sulfate) were introduced as an aqueous solution. In the concentrated emulsion polymerization, a mixture of the monomers containing dissolved oxidant was first used as the dispersed phase of a concentrated emulsion in water, and the aqueous solution of reductants was subsequently added to the concentrated emulsion. In both cases, the polymerization started at room temperature, just after the reductants were introduced. Because the reactor was insulated, the heat generated by the reaction was mostly used to accelerate the polymerization, which reached a high conversion in 30 min. The effects of various parameters on the polymerization were investigated. Optimum values were found for the volume fraction of the dispersed phase, for the wt ratios of the two reductants and of the oxidant to reductants, and for the surfactant and reductant concentrations. One concludes that the concentrated emulsion polymerization method is particularly suitable for the room temperature-initiated, self-heating polymerization. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 999–1011, 1998