Regenerative Behaviors of Cokes-Deposited Ferrierite Zeolite during Gas-Phase Fluidized-Bed DME Carbonylation Reaction

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Authors: Hyun Seung Jung, Rong Zhao, Woo Chang Sung, Ji Min Kim, Jun Young Kim, Noritatsu Tsubaki, Dong Hyun Lee, Jong Wook Bae
Cited by: 2
References: 57

Abstract

Gas-phase dimethyl ether (DME) carbonylation to methyl acetate (MA) is prone to be deactivated by coke depositions on Brønsted acid sites (Si-OH-Al groups) of ferrierite zeolite, and those inevitable coke depositions on the active sites, especially in eight-membered ring (8-MR) channels, are required to be regenerated through in situ removal of coke precursors in a circular fluidized-bed reactor (FBR) for its stable operation. The bench-scale FBR system was applied to verify optimal regenerative treatment conditions and to study behaviors of spray-dried FER zeolites ∼60 μm in size after regeneration. Those inactive coke precursors were effectively removed with small structural disintegrations of the FER zeolite under an air environment at 500 °C at a slow ramping rate of 1 °C/min among the tested range of 1–25 °C/min. Although the high regeneration temperature (∼500 °C) compared to the lower regeneration temperature of 300–400 °C caused slight decreases of Si-OH-Al sites assigned to Brønsted acid sites, the catalytic activity was almost recovered at those optimal regeneration conditions with an almost complete removal of coke precursors. The stable maintenance of active sites and original sphere shapes was clearly observed during 5 successive cycles of gas-phase DME carbonylation reaction at 240 °C and regenerative treatment at ∼500 °C at a fixed pressure of 5.0 MPa, which were attributed to the appropriate removal of surface coke precursors in the 8-MR channels without any significant structural disintegration.

Fields of Study & Subjects

Zeolite Catalysis and Synthesis Catalysts for Methane Reforming Fiber-reinforced polymer composites

Publication details

Journal / source
Energy & Fuels
Publisher
American Chemical Society (ACS)
Volume
40
Issue
4
Pages
2203–2212
Publication date
19 January 2026
Language
EN