Isothermal emulsion polymerization of n‐butyl methacrylate with KPS and redox initiators: Kinetic study at different surfactant/initiator concentrations and reaction temperature |
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| Authors: | Shi Wang Eric S. Daniels E. David Sudol Andrew Klein Mohamed S. El‐Aasser |
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| Affiliation: | 1. Emulsion Polymer Institute, Lehigh University, Bethlehem, Pennsylvania;2. Department of Chemical Engineering, Lehigh University, Bethlehem, Pennsylvania |
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| Abstract: | Thermal initiators, although widely used in emulsion polymerization, are limited to high reaction temperatures due to their high activation energy. Redox initiators have low activation energies indicating that emulsion polymerization could be conducted at lower temperatures to save energy. In the present study, a redox initiator system comprised of hydrogen peroxide (H2O2) and ascorbic acid (AA) in conjunction with a Fe2+ ion catalyst is compared with a potassium persulfate (KPS) thermal initiator in an emulsion polymerization system consisting of n‐butyl methacrylate (BMA), sodium lauryl sulfate (SLS) and water. The dependence of particle number on surfactant and initiator concentrations shows that redox‐ and KPS‐initiated systems both follow the Smith‐Ewart theory. However, the high radical flux generated from the redox initiator results in the formation of much smaller latex particles and higher reaction rate with lower molecular weights. Latex particle size and molecular weight could also be influenced by reaction temperature. By using redox initiator, small monodisperse particles (diameter < 50 nm) can be achieved without using a large amount of surfactant. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43037. |
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| Keywords: | colloids emulsion polymerization kinetics radical polymerization |
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