Highly Efficient Conversion of CO <sub>2</sub> to C <sub>2</sub> –C <sub>4</sub> Olefins on Co- and Zn-Copromoted Na-Modified Fe <sub>2</sub> O <sub>3</sub> Catalysts with Suppressed In Situ Oxidation of Fe <sub>5</sub> C <sub>2</sub>

High Resolution Image Download MS PowerPoint Slide The hydrogenation of CO 2 to higher hydrocarbons (C 2+ -hydrocarbons), especially to C 2 –C 4 olefins, represents an effective strategy for the high-value utilization of this renewable raw material. Although Fe-based catalysts are typically used for this reaction and demonstrate promising industrial performance, they are prone to deactivation due to H 2 O-mediated oxidation of the catalytically active Fe 5 C 2 phase under reaction conditions. In this regard, we introduce two transition-metal promoters, Co and Zn, to enhance the on-stream stability of Na-modified Fe-based catalysts. The developed Na–Fe 3 Co 1 Zn 1 catalyst achieved a space-time yield of the formation of C 2 –C 4 olefins of 27.6 mmol·g cat –1 ·h –1 at 47.1% CO 2 conversion at 340 °C and 20 bar using an industrially relevant feed. This productivity is about 2 times higher than that of the undoped Na–Fe catalyst and remains stable over 120 h on stream, placing it among the most effective state-of-the-art catalysts reported to date. This catalyst also achieves a higher yield of C 2+ hydrocarbons compared to most previously developed catalysts, while the yields of CO and CH 4, which are side products, are markedly lower.

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Publication Details

Journal
ACS Catalysis
Published
2026-07-16
DOI
https://doi.org/10.1021/acscatal.6c04291
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
0.00

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article

Highly Efficient Conversion of CO 2 to C 2 –C 4 Olefins on Co- and Zn-Copromoted Na-Modified Fe 2 O 3 Catalysts with Suppressed In Situ Oxidation of Fe 5 C 2

Haoyang Xu, Evgenii V. Kondratenko, Hui Li, Minghui Tang et al.
ACS Catalysis
Catalysts for Methane Reforming
article

Highly Efficient Conversion of CO 2 to C 2 –C 4 Olefins on Co- and Zn-Copromoted Na-Modified Fe 2 O 3 Catalysts with Suppressed In Situ Oxidation of Fe 5 C 2

Haoyang Xu, Evgenii V. Kondratenko, Hui Li, Minghui Tang, Zi Wang, Qi Liu, Shengyong Lu
article en

Abstract

High Resolution Image Download MS PowerPoint Slide The hydrogenation of CO 2 to higher hydrocarbons (C 2+ -hydrocarbons), especially to C 2 –C 4 olefins, represents an effective strategy for the high-value utilization of this renewable raw material. Although Fe-based catalysts are typically used for this reaction and demonstrate promising industrial performance, they are prone to deactivation due to H 2 O-mediated oxidation of the catalytically active Fe 5 C 2 phase under reaction conditions. In this regard, we introduce two transition-metal promoters, Co and Zn, to enhance the on-stream stability of Na-modified Fe-based catalysts. The developed Na–Fe 3 Co 1 Zn 1 catalyst achieved a space-time yield of the formation of C 2 –C 4 olefins of 27.6 mmol·g cat –1 ·h –1 at 47.1% CO 2 conversion at 340 °C and 20 bar using an industrially relevant feed. This productivity is about 2 times higher than that of the undoped Na–Fe catalyst and remains stable over 120 h on stream, placing it among the most effective state-of-the-art catalysts reported to date. This catalyst also achieves a higher yield of C 2+ hydrocarbons compared to most previously developed catalysts, while the yields of CO and CH 4, which are side products, are markedly lower.

ACS Catalysis
Huaneng Clean Energy Research Institute (CN), Zhejiang Energy Research Institute (CN), Leibniz Institute for Catalysis (DE), State Key Laboratory of Clean Energy Utilization, Zhejiang University (CN), Taizhou University (CN)
Deutsche Forschungsgemeinschaft, Helmholtz Association
Affordable and clean energy
Openalex Percentile: Top 24%
Catalysts for Methane Reforming
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