Abstract
Propylene was copolymerized with allylanisole (AA) using Me 2Si(Ind)2ZrCl2 and Et(Ind)2ZrCl 2, and the methylaluminoxane MAO cocatalyst at 70 °C and a cocatalyst to catalyst (Al:Zr) molar ratio of 1000. It was fed at 8.5 bar(g). The weight-average molecular weight, M̄w, for both metallocenes decreased as the AA teed concentration increased. Therefore, allylanisole acted as an in situ chain transfer agent. The chain transfer constants, k tr/kp, of AA for Et(Ind)2ZrCl2 and Me2Si(Ind)2ZrCl2 turned out to be 0.33 and 0.40, respectively. The characterization of the resulting products by 1HNMR demonstrated that AA end-capped the isotactic poly(propylene) chains which showed to be low molecular weight oligomers; 4.96 × 10 3 ≤ M̄w ≤ 9.80 × 103. An appropriate chain transfer mechanism for AA has been proposed.
| Original language | English |
|---|---|
| Pages (from-to) | 334-338 |
| Number of pages | 5 |
| Journal | Macromolecular Reaction Engineering |
| Volume | 2 |
| Issue number | 4 |
| DOIs | |
| State | Published - 28 Jul 2008 |
ASJC Scopus subject areas
- General Chemistry
- General Chemical Engineering
- Polymers and Plastics
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