Author(s) |
Fellows, Christopher
Murison, Robert D
Russell, Gregory
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Publication Date |
2011
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Abstract |
Analysis of published experimental data on monomeric radical diffusion in the emulsion polymerisation of styrene shows that it can be quantitatively described equally well by non-equilibrium diffusion from particles, where all parameters are derived from properties of the discrete phase, or by steady-state diffusion where all parameters are derived from properties of the continuous phase. The non-equilibrium model better describes an observed experimental trend to a reduced desorption rate coefficient at higher weight fraction of polymer in the particles. The theoretical upper bound of the non-equilibrium model is also higher than the theoretical upper bound of the steady-state model allowing fits to experimental data which must be discarded as anomalous in the continuous phase model.
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Citation |
Macromolecular Theory and Simulations, 20(6), p. 425-432
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ISSN |
1521-3919
1022-1344
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Link | |
Publisher |
Wiley-VCH Verlag GmbH & Co KGaA
|
Title |
Model Discrimination of Radical Desorption Kinetics in Emulsion Polymerisation
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Type of document |
Journal Article
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Entity Type |
Publication
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