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Original Paper | Open Access

Reaction characteristics of maximizing light olefins and decreasing methane in C5 hydrocarbons catalytic pyrolysis

Mei-Jia Liua, Gang Wanga( ), Shun-Nian Xua, Tao-Ran Zhenga, Zhong-Dong Zhangb( ), Sheng-Bao Heb
State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing, 102249, China
Petrochemical Research Institute, PetroChina, Beijing, 102206, China

Edited by Jia-Jia Fei

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Abstract

When converting C5 hydrocarbons to light olefins by catalytic pyrolysis, the generation of low value-added methane will affect the atomic utilization efficiency of C5 hydrocarbons. To improve the atomic utilization efficiency, different generation pathways of light olefins and methane in the catalytic pyrolysis of C5 hydrocarbons were analyzed, and the effects of reaction conditions and zeolite types were investigated. Results showed that light olefins were mainly formed by breaking the C2–C3 bond in the middle position, while methane was formed by breaking the C1–C2 bond at the end. Meanwhile, it was discovered that the hydrogen transfer reaction could be reduced by about 90% by selecting MTT zeolite with 1D topology and FER zeolite with 2D topology under high weight hourly space velocity (WHSV) and high temperature operations, thus leading to the improvement of the light olefins selectivity for the catalytic pyrolysis of n-pentane and 1-pentene to 55.12% and 74.60%, respectively. Moreover, the fraction ratio of terminal C1–C2 bond cleavage was reduced, which would reduce the selectivity of methane to 6.63% and 1.83%. Therefore, zeolite with low hydrogen transfer activity and catalytic pyrolysis process with high WHSV will be conducive to maximize light olefins and to decrease methane.

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Petroleum Science
Pages 1909-1921

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Cite this article:
Liu M-J, Wang G, Xu S-N, et al. Reaction characteristics of maximizing light olefins and decreasing methane in C5 hydrocarbons catalytic pyrolysis. Petroleum Science, 2023, 20(3): 1909-1921. https://doi.org/10.1016/j.petsci.2022.11.026

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Received: 09 June 2022
Revised: 31 July 2022
Accepted: 30 November 2022
Published: 05 December 2022
© 2023 The Authors.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).