Abstract
We report the first synthesis of poly (N-methylolacrylamide) (PNMA) via free-radical frontal polymerization (FP) with solid monomers at ambient pressure. The appropriate amounts of reactants (N-methylolacrylamide) (NMA) and initiator (ammonium persulfate) were mixed together at ambient temperature without solvent. FP was initiated by heating the wall of the tube with a soldering iron, and the resultant hot fronts were allowed to self-propagate throughout the reaction vessel. Once initiated, no further energy was required for polymerization to occur. To suppress the fingers of molten monomer, a small amount of nanosilica was added. We also produced PNMA with dimethyl sulfoxide (DMSO) or N-methyl-2-pyrrolidone, as solvent by FP, to study the macrokinetics in FP of PNMA without fillers. The front velocity and front temperature dependence on the ammonium persulfate and N-methyl-2-pyrrolidone concentration were investigated. The polymer was analyzed by thermogravimetric analysis. Results show that without postpolymerization solvent removal, waste production can be reduced. Solvent-free FP could be exploited as a means for preparation of PNMA with the potential advantage of higher throughput than solventbased methods.
Original language | English |
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Pages (from-to) | 4322-4330 |
Number of pages | 9 |
Journal | Journal of Polymer Science, Part A: Polymer Chemistry |
Volume | 45 |
Issue number | 18 |
DOIs | |
State | Published - 15 Sep 2007 |
Keywords
- Ammonium persulfate
- Frontal polymerization (FP)
- Kinetics (polym.)
- Nanosilica
- Poly(N-methylolacrylamide) (PNMA)
- Polyamides
- Radical polymerization
- Self-sustaining
- Solid monomers
- Solid-state polymerization