Microemulsion polymerization: Phase behavior driven mechanistic changes

Oliver Lade, Carlos C. Co, Patricia Cotts, Reinhard Strey, Eric W. Kaler

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

We have examined the phase behavior of anionic microemulsions of the general type water/NaCl-hexyl methacrylate (C6 MA)-bis(2-ethylhexyl)sulfosuccinate (AOT)/sodium dodecyl sulfate (SDS) with respect to temperature and composition. Monomer partitioning measurements and kinetic experiments show good agreement with the Morgan model (de Vries et al. in Macromolecules 34:3233, 2001) for droplet-type microemulsions that do not phase separate as monomer is consumed. In contrast, balanced microemulsions, which efficiently solubilize large amounts of monomer, exhibit dramatic effects on the polymerization kinetics as the phase behavior changes. Our findings suggest that the appearance of a liquid crystalline mesophase in the binary water-surfactant system of the respective microemulsion causes a phase separation during polymerization and, thus, a severe deviation from previous mechanistic models.

Original languageEnglish (US)
Pages (from-to)905-916
Number of pages12
JournalColloid and Polymer Science
Volume283
Issue number8
DOIs
StatePublished - May 1 2005

Keywords

  • Alkyl methacrylate
  • Emulsification-failure boundary
  • Ionic surfactant
  • Kinetics
  • Mechanism
  • Microemulsion polymerization
  • Phase behavior
  • Phase inversion temperature

Fingerprint Dive into the research topics of 'Microemulsion polymerization: Phase behavior driven mechanistic changes'. Together they form a unique fingerprint.

Cite this