Acid Strength Controlled Reaction Pathways for the Catalytic Cracking of 1‑Pentene to Propene over ZSM‑5
journal contributionposted on 02.07.2015, 00:00 by Long F. Lin, Shu F. Zhao, Da W. Zhang, Hui Fan, Yue M. Liu, Ming Y. He
The influence of acid strength was evaluated toward the selectivity to propene on conversion of 1-pentene. For the catalytic cracking of 1-pentene, the main reaction pathways and the molar ratio of propene to ethene (P/E ratio) were controlled by acid strength with the appropriate amount of total acid sites. The results showed that the P/E ratio increased with decreasing amounts of strong acid sites, since the activation energies of individual reaction pathways were influenced by acid strength to a different extent. Strong acid sites could promote pathway I′ (C52– → C22– + C32–) and pathway II′-1 (C62– → C22– + C42–), while weak acid sites preferred pathway II′ (2C52– → C10+ → C42– + C62–) and pathway II′-2 (C62– → 2C32–), since pathways II′ and II′-2 underwent some energetically favorable routes (tertiary–secondary, secondary–secondary) of carbenium ion intermediates. By manipulation of the acid strength distribution on ZSM-5, the P/E ratio and selectivity of propene could be significantly improved, suggesting that this can provide an important guideline for improving such a process. In addition, we also designed a coupled process combing butene and pentene coconversion, as pentene and butene could be produced during C42– and C52– catalytic cracking. The coupled process could offer a promising solution to gain high selectivity of propene from C4 and C5 olefin cracking.