Abstract
A screening of macroreticular ion exchange resins has been carried out in order to select the most suitable catalysts for liquid-phase oligomerization of an isoamylene mixture. The reaction was performed at mild temperature (343 K) to promote the dimerization and trimerization, and at higher temperature (383 K) to evaluate side reactions like cracking and copolymerization. No compounds higher than trimers were significantly detected at studied conditions. By plotting product yields versus conversion at 343 K, it was showed no significant differences between all catalysts tested. However, at 383 K, the ion exchange resins which mainly work in the external zone were more selective to dimerization and less to cracking and trimerization products, which suggests that trimerization and cracking mainly took place inside the gel-phase of the macroreticular resins. The most active catalysts were the oversulfonated resins with high cross-linking degree and high acid capacity. A heterogeneous Eley-Rideal kinetic model showed better fitting of dimerization rates than two pseudo-homogeneous models.
| Original language | English |
|---|---|
| Pages (from-to) | 163-171 |
| Number of pages | 9 |
| Journal | Applied Catalysis A: General |
| Volume | 435-436 |
| DOIs | |
| Publication status | Published - 5 Sept 2012 |
Funding
This work was supported by funds of the Ministry of Science and Technology, Spain (Project CTQ2004-03165/PPQ). Authors are thankful for this financial support. We also grateful to Room & Haas and to Purolite for providing kindly the ion exchange resins used in this research.
Keywords
- Ion exchange resins
- Isoamylene
- Oligomerization