Abstract
AbstractConversion–time data were obtained for the polymerization of acrylamide initiated by the redox couple persulfate–thiosulfate by using a dilatometer. A plot of initial rate as a function of thiosulfate concentration shows a well‐defined maximum and three distinct regions of behavior. In each region the shape of the conversion–time curves demonstrates the differences in apparent order with respect to monomer arising from changes in initiator concentration during an individual run. A reaction mechanism is proposed to explain the results, and a limiting form of the rate expression is derived for each of the three regions. The ranges of concentration studied are: persulfate, 9.5 × 10−4−4.7 × 10−2M; thiosulfate, 2 × 10−5−2 × 10−2M; initial monomer, 0.05–1.0M; and temperature, 30–50°C. Within these ranges the initial rate shows a halforder dependence on persulfate and a first‐order dependence on initial monomer concentration.
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