Abstract
AbstractThe starch–polyacrylonitrile graft copolymer prepared from gelatinized wheat starch with ceric ammoninm nitrate as the initiator has been freed of ungrafted polyacrylonitrile and separated into fractions by extraction with dimethylformamide, γ‐butyrolactone, and dimethyl sulfoxide. The copolymer fractions obtained differed appreciably in level of add‐on, molecular weights of grafted chains, and grafting frequency. To determiue the molecular weights of grafted chains, the starch part of the copolymer was effectively removed by hydrolysis with α‐amylase. It was necessary to dissolve or swell the polymer in dimethyl sulfoxide and freshly precipitate it by addition to water before enzymatic hydrolysis. In studying the effect of reaction medium on copolymer composition, there was less ungrafted homopolymer formed and a higher yield of graft copolymer possessing more frequent grafts with water than with aqueous dimethylformamide or aqueous ethylene glycol. Polymer solubility, the results of control polymerizations of acrylonitrile in the absence of starch, and the detection of glucose endgroups on the polyacrylonitrile liberated from the fractionated polymer by hydrolysis are presented as evidence that the copolymers obtained are true grafts rather thau intimate mixtures.
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