Related Experiment Video
Updated: Jan 12, 2026

Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells
Published on: September 20, 2012
Coke-induced deactivation in zeolite catalysts: mechanisms, anti-coking modifications, and regeneration approaches
Mengdi Zhang1, Jing Huang1, Fanshuo Meng1
1State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing 211816, China. zunmin.zhang@njtech.edu.cn.
Abstract:
Zeolite catalysts, widely employed in petrochemical and refining processes, inevitably undergo gradual deactivation. Among the various deactivation pathways, coke-induced deactivation is the most critical, arising from the progressive deposition of carbonaceous species on acid sites and the subsequent blockage of micropores. The characteristics, mechanisms, and kinetics of coke formation are strongly influenced by the zeolite structure, acidity properties, and operating conditions, highlighting the need for a molecular-level understanding to guide catalyst design and regeneration. This review summarizes the recent advances in coke-induced deactivation of zeolite catalysts by covering the mechanisms and physicochemical characteristics of coke formation, strategies for enhancing coke resistance through rational catalyst design, and state-of-the-art regeneration approaches. By bridging fundamental insights and practical strategies, this work aims to support the development of durable zeolite catalysts and efficient regeneration schemes for sustainable industrial applications.
Related Concept Videos
Catalysis
Pozzolans
Fly ash is...
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Aldehydes and Ketones to Alkanes: Wolff–Kishner Reduction
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

