Inverse dispersion polymerizations of acrylic acid were conducted by using a water-soluble redox initiation system under both isothermal and nonisothermal conditions. The polymerizations were monitored by measuring residual monomer by highperformance liquid chromatography for isothermal polymerizati
Kinetics of redox polymerizations of acrylic acid in inverse dispersion and in aqueous solution
β 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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β¦ 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.
π SIMILAR VOLUMES
Aqueous polymerization of acrylic acid was conducted using potassium bromate/sodium metabisulphite redox initiators under isothermal conditions. The initial polymerization rates were determined with variation in temperature and in the initial concentrations of acrylic acid, potassium bromate and sod
## 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)β__n__βpropanol (__n__PA) and ACNβethanol as redox initiator systems. The cericβion consumption was firstβorder with respect to th