Abstract
Molecular weight and particle size distributions of latexes prepared by free radical polymerization of n-butyl methacrylate, tert-butyl methacrylate, n-hexyl methacrylate, and styrene in aqueous microemulsions of dodecyltrimethylammonium bromide surfactant are measured using GPC/ MALLS, QLS, and cryo-TEM. The results are compared to a molecular weight distribution model derived from the monomer partitioning and kinetic studies described in the accompanying papers. Polystyrene with weight-average molecular weights of ∼15 × 106 Da, which are 7 times greater than the limiting molecular weight imposed by chain transfer to monomer, are consistently obtained. Diffusion-limited exit of monomer radicals, generated by chain transfer, to the aqueous phase coupled with chain transfer to polymer are likely reasons for the enhanced polystyrene molecular weights.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3245-3254 |
| Number of pages | 10 |
| Journal | Macromolecules |
| Volume | 34 |
| Issue number | 10 |
| DOIs | |
| State | Published - May 8 2001 |
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