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142 Advances in Polymer Science Editorial Board: A. Abe. A.-C ...

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44 B. Charleux, R. Faust<br />

Scheme 8<br />

3.1.2.4<br />

Poly(styrene) and poly(a-methylstyrene) Branches<br />

EPDM graft terpolymers with PS or poly(a-MeS) branches were prepared from<br />

chlor<strong>in</strong>ated commercial EPDM polymer (7.7% 5-ethylidene-2-norbornene as<br />

diene, M n=50,000 g mol –1 ) <strong>in</strong> conjunction with Et 2AlCl, us<strong>in</strong>g the “graft<strong>in</strong>g<br />

from” technique [66]. Graft<strong>in</strong>g could only be achieved <strong>in</strong> the presence of 10–20%<br />

polar solvent, e.g., CH 3 Cl or CH 2 Cl 2 ; <strong>in</strong> pure heptane no graft copolymer could<br />

be isolated. The graft<strong>in</strong>g reaction was carried out at –30 °C, below this temperature<br />

the EPDM polymer was not soluble <strong>in</strong> the mixed heptane/polar solvent<br />

used. The graft<strong>in</strong>g efficiencies were determ<strong>in</strong>ed by selective solvent extraction<br />

and found to be quite low, <strong>in</strong> the range of 10–20%. The tensile strength and ultimate<br />

elongation were also determ<strong>in</strong>ed and found to be quite low when the<br />

amount of PS was 50 wt%, although at the expense of the elastomeric<br />

properties (<strong>in</strong>creased modulus and decreased ultimate elongation).<br />

3.2<br />

“Graft<strong>in</strong>g Onto” Technique<br />

In the “graft<strong>in</strong>g onto” technique, the macromolecular branches are l<strong>in</strong>ked to the<br />

ma<strong>in</strong> cha<strong>in</strong> by specific reaction between their a or w end group and reactive<br />

functional groups <strong>in</strong> the backbone.

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