Abstract
This review considers the mechanism of multilayered coke formation on catalysts of various types and analyzes its possible variants. A detailed derivation of equations of the dynamics of accumulation for different types of coke and the kinetics of its deactivating effect is given. The substantiated dependences of the relative activity of a catalyst on the concentration of coke are derived. Specific examples of these dependences are presented. They confirm the advantages of rigorous models based on the mechanism of the phenomenon in comparison with the formal description of experiments, which does not have predictive power.
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Dedicated to the blessed memory of R.A. Buyanov
Translated by V. Makhlyarchuk
Abbreviations and notation: TPO, temperature-programmed oxidation; EM, electron microscopy; EELS, electron energy loss spectroscopy; FTIR, Fourier transform infrared spectroscopy; NMR, nuclear magnetic resonance; AES, Auger electron spectroscopy; XRD, X-ray diffraction; XPS, X-ray photoelectron spectroscopy; EPR, electron paramagnetic resonance; CNT, carbon nanotube; SWCNT, single-walled carbon nanotube; MWCNT, multi-walled carbon nanotube; MCP, methylcyclopentane; CH, cyclohexane; n-C6, n-hexane; B, benzene; MTO, methanol conversion to olefins.
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Ostrovskii, N.M. Coking of Catalysts: Mechanisms, Models, and Influence. Kinet Catal 63, 52–66 (2022). https://doi.org/10.1134/S0023158422010062
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DOI: https://doi.org/10.1134/S0023158422010062