Methylcyclohexane transformation over HMCM22 zeolite: Mechanism and location of the reactions

At 350 °C, over a HMWW zeolite image, methylcyclohexane (mch) transforms into four types of products: isomers (I), C1–C8 aliphatic hydrocarbons (C), benzenic hydrocarbons (A), and trapped carbonaceous compounds (coke). The role played by the various micropores was established through a two-step method: deactivation of supercages by coking and poisoning of the outer hemicage sites by 2,4-dimethylquinoline. More than 85% of mch transformation occurs in the supercages, ∼11% occurs in the outer hemicages, and only <2% occurs in the sinusoidal channels, which, considering the protonic site distribution, corresponds to turnover frequency values of 33, 82, and 2 h−1. The product distributions are very different: I, C3–C5 branched alkanes, and coke in similar amounts; essentially I and C3–C8 branched alkanes; and mainly C1–C8 and A products. The carbenium ion chain mechanism can account for the products formed in supercages and hemicages, whereas protolytic mechanisms play an important role in the narrow sinusoidal channels. Deactivation by coking is very fast in supercages and negligible in the other locations.