Abstract
The formation of coke as a result of propene transformation at 623 K on zeolites results from a product shape selectivity mechanism of which the products are polyaromatic molecules, such as pyrene on MFI, anthracene on MOR, pyrene and coronene on FAU. Zeolite regeneration can be achieved by using non-thermal plasma (NTP), with decreased energy consumption, employing a fixed bed dielectric barrier reactor. The efficiency of this alternative regeneration process depends on the coke toxicity. On MFI and FAU (featuring three-dimensional 10 and 12 ring channel systems, respectively) coking occurs by poisoning the Brønsted acid sites; on MOR, (presenting a one-dimensional 12 ring channel system) pore blocking takes place, leading to higher coke toxicity. A complete coke removal is achieved on MFI and FAU zeolites using NTP within 3 h, while for MOR coke, removal proceeds slower and is incomplete after 3 h on stream. Hence, the efficiency of regeneration is impacted by the accessibility of active oxygenated species generated under plasma (e.g., O*, O2+) to coke molecules.
Subject
Physical and Theoretical Chemistry,Catalysis
Cited by
9 articles.
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