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Interfacial Mass Transfer in Nitroxide‐Mediated Miniemulsion Polymerization
Author(s) -
Ma John W.,
Cunningham Michael F.,
McAuley Kim B.,
Keoshkerian Barkev,
Georges Michael K.
Publication year - 2002
Publication title -
macromolecular theory and simulations
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.37
H-Index - 56
eISSN - 1521-3919
pISSN - 1022-1344
DOI - 10.1002/1521-3919(200211)11:9<953::aid-mats953>3.0.co;2-d
Subject(s) - miniemulsion , nitroxide mediated radical polymerization , polymerization , chain transfer , polymer chemistry , chemistry , radical polymerization , reversible addition−fragmentation chain transfer polymerization , polymer science , chemical engineering , polymer , organic chemistry , engineering
A mathematical model has been developed to describe the interfacial mass transfer of TEMPO in a nitroxide‐mediated miniemulsion polymerization (NMMP) system in the absence of chemical reactions. The model is used to examine how the diffusivity of TEMPO in the aqueous and organic droplet phases, the average droplet diameter and the nitroxide partition coefficient influences the time required for the nitroxide to reach phase equilibrium under non‐steady state conditions. Our model predicts that phase equilibrium is achieved quickly (< 1 × 10 −4 s) in NMMP systems under typical polymerization conditions and even at high monomer conversions when there is significant resistance to molecular diffusion. The characteristic time for reversible radical deactivation by TEMPO was found to be more than ten times greater than the predicted equilibration times, indicating that phase equilibrium will be achieved before TEMPO has an opportunity to react with active polymer radicals. However, significantly longer equilibration times are predicted, when average droplet diameters are as large as those typically found in emulsion and suspension polymerization systems, indicating that the aqueous and organic phase concentrations of nitroxide may not always be at phase equilibrium during polymerization in these systems.Influence of droplet phase TEMPO diffusivity, D TEMPO,drop , on the predicted organic phase concentration of TEMPO.