Polymerization and copolymerization in associated monomer aggregates

✍ Scribed by A. Chapiro

• Publisher: Elsevier Science
• Year: 1973
• Tongue: English
• Weight: 629 KB
• Volume: 9
• Category: Article
• ISSN: 0014-3057
• DOI: 10.1016/0014-3057(73)90044-x

✦ Synopsis

The polymerization of acrylic acid in bulk is controlled by linear plurimolecular H-bonded aggregates of the monomer which lead to the formation of a syndiotactic polymer. Polar solvents do not dissociate these aggregates unless high dilutions are reached. In contrast, "normal" kinetics are observed in the presence of 10-20 per cent toluene, n-hexane or chloroform. The polymerization of methacrylic acid is not affected to the same extent by molecular aggregates. In the copolymerization of acrylic acid with methyl acrylate or acrylonitrile, the reactivity ratios are altered by solvents. The acrylic acid content is higher in copolymers formed in bulk than in toluene solution. But similar effects are observed in the presence of DMF which does not dissociate the aggregates of acrylic acid; moreover, copolymerization data obtained with methacrylic acid indicate that other factors may be involved in determining reactivity ratios.

Acrylamide also forms H-bonded aggregates and its eopolymerization behaviour is strongly affected by solvents. No simple correlation holds, however, between reactivity ratios and extent of association.

A very strict control of chain propagation occurs when 4-vinylpyridine is polymerized in the presence of polycarboxylic acids. A considerable rate increase was observed when vinylpyridine was grafted into polytetrafluoroethylene films which contained poly(acrylic acid) branches. This effect is explained by assuming that the pyridine groups form strong associations with the carboxylic sites, thereby providing a very favourable orientation of the vinyl groups for chain propagation.