Fellows, Christopher

Murison, Robert D

Russell, Gregory

2011

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.

Macromolecular Theory and Simulations, 20(6), p. 425-432

1521-3919

1022-1344

https://hdl.handle.net/1959.11/9128

en

Wiley-VCH Verlag GmbH & Co KGaA

Model Discrimination of Radical Desorption Kinetics in Emulsion Polymerisation

Journal Article

Publication