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Cationic chain polymerization counterion effects

For any specific type of initiation (i.e., radical, cationic, or anionic) the monomer reactivity ratios and therefore the copolymer composition equation are independent of many reaction parameters. Since termination and initiation rate constants are not involved, the copolymer composition is independent of differences in the rates of initiation and termination or of the absence or presence of inhibitors or chain-transfer agents. Under a wide range of conditions the copolymer composition is independent of the degree of polymerization. The only limitation on this generalization is that the copolymer be a high polymer. Further, the particular initiation system used in a radical copolymerization has no effect on copolymer composition. The same copolymer composition is obtained irrespective of whether initiation occurs by the thermal homolysis of initiators such as AIBN or peroxides, redox, photolysis, or radiolysis. Solvent effects on copolymer composition are found in some radical copolymerizations (Sec. 6-3a). Ionic copolymerizations usually show significant effects of solvent as well as counterion on copolymer composition (Sec. 6-4). [Pg.471]

This marked sensitivity of the stereochemistry of anionic polymerization to the nature of the counterion and solvent can be traced to the structure of the propagating chain end. The latter involves a carbon-metal bond which can have variable characteristics, ranging all the way from highly associated species with covalent character to a variety of ionic species (Hsieh and CJuirk, 1996). The presence of a more electropositive metal and/or a cation-solvating solvents, such as ethers, can effect a variety of changes in the nature of the carbanionic chain end (a) the degree of association of the chain ends can decrease or be eliminated (b) the interaction of the cation with the anion can be decreased... [Pg.76]

The termination reactions in cationic polymerizations can often lead to low molecular weight products. This can be a result from various effects. Also, the counterions may be involved in the terminations [126]. Thus, with some Lewis acids, the polymer cation may react with the counterion by abstracting a halogen. An example of that is polymerization of isobutylene with BCI3. In this reaction, termination by chain transferring is absent [126]. Instead, the following mechanism takes place [127] ... [Pg.177]


See other pages where Cationic chain polymerization counterion effects is mentioned: [Pg.231]    [Pg.735]    [Pg.209]    [Pg.428]    [Pg.5601]    [Pg.482]    [Pg.412]    [Pg.48]    [Pg.53]    [Pg.172]    [Pg.207]    [Pg.207]    [Pg.428]    [Pg.328]    [Pg.368]    [Pg.104]    [Pg.513]    [Pg.26]   
See also in sourсe #XX -- [ Pg.403 ]

See also in sourсe #XX -- [ Pg.403 ]




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Cation counterions

Cation effect

Cationic chain polymerization

Cationic effect

Cationic polymerization

Cationic polymerization polymerizations

Chain effect

Counterion

Counterion effects

Counterions

Counterions, polymeric

Effective chain

Polymerization effect

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