Experimental study and numerical simulation on a multi-stage counter-current continuous fluidized bed reactor for activating iron-based Fischer-Tropsch synthesis catalyst

Rapid and robust activation of iron-based catalysts is critical for industrial Fischer-Tropsch synthesis. This work introduces a multi-stage, counter-current continuous fluidized-bed system that enables uninterrupted catalyst activation, addressing key limitations of conventional batch fluidized beds. Compared with previous studies that mainly addressed batch activation or conventional fluidized-bed activation, the novelty of this work lies in the combined cold-flow, CFD, and hot-flow validation of a multi-stage counter-current continuous fluidized-bed reactor for iron-based catalyst activation. Cold-flow tracer-based RTD experiments were conducted in a transparent acrylic reactor, and hot-flow activation tests were performed in a stainless-steel reactor under syngas at 265 °C and 0.2 MPa. Cold-flow experiments show that the inter-stage overflow design ensures unidirectional particle transfer, markedly suppresses back-mixing, and improves plug-flow behavior. The dimensionless variance of the residence time distribution decreases from 1.0 to 0.475, while the fitted tanks-in-series number increases from 1.0 to 2.34. CFD simulations accurately reproduce the observed hydrodynamics and extend the analysis to operating limits, predicting an upper gas-velocity threshold of 0.29 m/s under cold-flow conditions. Hot-flow simulations based on the validated model identify a slightly lower limit of 0.27 m/s, which provides practical guidance for reactor design and scale-up. Hot-flow experiments confirm stable fluidization at 265 °C and 0.2 MPa with continuous catalyst feeding and withdrawal. The catalysts activated in the multi-stage continuous system exhibit CO conversions of 51 to 53% and CH 4 selectivities of approximately 1% in a stirred-tank evaluation reactor, achieving performance comparable to that obtained with our batch fluidized bed activation method.

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Publication Details

Journal
Chemical Engineering Journal
Published
2026-06-30
DOI
https://doi.org/10.1016/j.cej.2026.178483
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
0.00

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article

Experimental study and numerical simulation on a multi-stage counter-current continuous fluidized bed reactor for activating iron-based Fischer-Tropsch synthesis catalyst

Yifeng Bu, Youwei Cheng, Zhuowu Men, Ruili Tong et al.
Chemical Engineering Journal
Catalysts for Methane Reforming
article

Experimental study and numerical simulation on a multi-stage counter-current continuous fluidized bed reactor for activating iron-based Fischer-Tropsch synthesis catalyst

Yifeng Bu, Youwei Cheng, Zhuowu Men, Ruili Tong, Chengxiang Li, Hairui Lin, Z L Yang, Yongmin Zhang, Tao Wang
article en

Abstract

Rapid and robust activation of iron-based catalysts is critical for industrial Fischer-Tropsch synthesis. This work introduces a multi-stage, counter-current continuous fluidized-bed system that enables uninterrupted catalyst activation, addressing key limitations of conventional batch fluidized beds. Compared with previous studies that mainly addressed batch activation or conventional fluidized-bed activation, the novelty of this work lies in the combined cold-flow, CFD, and hot-flow validation of a multi-stage counter-current continuous fluidized-bed reactor for iron-based catalyst activation. Cold-flow tracer-based RTD experiments were conducted in a transparent acrylic reactor, and hot-flow activation tests were performed in a stainless-steel reactor under syngas at 265 °C and 0.2 MPa. Cold-flow experiments show that the inter-stage overflow design ensures unidirectional particle transfer, markedly suppresses back-mixing, and improves plug-flow behavior. The dimensionless variance of the residence time distribution decreases from 1.0 to 0.475, while the fitted tanks-in-series number increases from 1.0 to 2.34. CFD simulations accurately reproduce the observed hydrodynamics and extend the analysis to operating limits, predicting an upper gas-velocity threshold of 0.29 m/s under cold-flow conditions. Hot-flow simulations based on the validated model identify a slightly lower limit of 0.27 m/s, which provides practical guidance for reactor design and scale-up. Hot-flow experiments confirm stable fluidization at 265 °C and 0.2 MPa with continuous catalyst feeding and withdrawal. The catalysts activated in the multi-stage continuous system exhibit CO conversions of 51 to 53% and CH 4 selectivities of approximately 1% in a stirred-tank evaluation reactor, achieving performance comparable to that obtained with our batch fluidized bed activation method.

Chemical Engineering JournalVol. 544
China University of Petroleum, Beijing (CN), National Institute of Clean and Low-Carbon Energy (CN), Ningxia Water Conservancy (CN), China Shenhua Energy (China) (CN), Zhejiang University (CN)
Ministry of Science and Technology of the People's Republic of China
Openalex Percentile: Top 21%
Catalysts for Methane Reforming
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