Influence of the functionality of the quaternizing agent and the polymer molecular weight on the viscoelastic behaviour of α,ω-(dimethylamino)-polyisoprenes

Quaternization of the end-groups of α,ω-(dimethylamino)polyisoprenes with monofunctional, difunctional and trifunctional halides (iodides and bromides) has been undertaken on polymers of different molecular weights (Mn = 6000 and 38000 gmol-l). The thermal stability of the ammonium end-groups is somewhat better when iodide counteranions are present. Quaternization increases the T~ of the material. This effect is more pronounced for low molecular weight chains, especially when a short alkyl group quaternizing agent is used. However, the size of the alkyl or aryl radical has a minor effect on polymer Tj when difunctional quaternizing agents are used. Nevertheless, the modulus of the rubber-like plateau of materials with difunctional agents is higher than with monofunctional quaternizing agents, owing to coupling reactions between the chain-ends. Rheological measurements indicate that the quaternized low molecular weight polyisoprenes exhibit an Arrhenius-type temperature dependence characterized by activation energies which vary between 121 and 146kJmol-1 and suggest that the relaxations attributed to dipole-dipole interactions dominate over long chain entanglements.