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Kinetics of redox polymerizations of acrylic acid in inverse dispersion and in aqueous solution

✍ Scribed by Zuifang Liu; Brian W. Brooks


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
263 KB
Volume
37
Category
Article
ISSN
0887-624X

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✦ Synopsis


Redox polymerizations of acrylic acid in inverse dispersion and in aqueous solution (with surfactant) were conducted by using sodium metabisulphite/potassium bromate initiators. The monomer conversions were determined by using high-performance liquid chromatography, and the polymer particles in the final lattices were examined using a scanning electron microscope with freeze-fracture equipment. Experimental rate expressions implied that complex reactions are involved in the redox polymerizations. A chemical reaction scheme was proposed, and kinetic models were developed for the redox polymerization in aqueous solution. Comparison between the experimental rate expressions and the kinetic models suggested a combination of bimolecular and monomolecular termination modes, a chain transfer function of the surfactant, and an oxidizing role of the oxygen molecules. The differences in the experimental rate expressions between the redox polymerization in inverse dispersion and that in aqueous solution are in good agreement with the kinetic model predictions.


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## Abstract A kinetic study of the aqueous polymerization of ethyl acrylate (EA) was carried out at 30Β°C in a dilute nitric acid medium with ammonium ceric nitrate (ACN)–__n__‐propanol (__n__PA) and ACN–ethanol as redox initiator systems. The ceric‐ion consumption was first‐order with respect to th