Dual-engine-driven realizing high-yield synthesis of Para-Xylene directly from CO2-containing syngas

The direct synthesis of light aromatics, especially para-xylene (p-X), from syngas/CO<sub>2</sub> is drawing strong interest, but improving the space-time yield (STY) of p-X is a significant challenge. Here, a dynamic "dual-engine-driven" (DED) catalytic system is designed by combining two partners of ZnCr and FeMn (named "dual-engine") with Z5@SiO<sub>2</sub> capsule zeolite. The DED catalyst of 1.0%FeMn&[ZnCr&Z5@SiO<sub>2</sub>] shows an extremely higher p-X STY of 36.1 g<sub>p-x</sub>·k<sub>gcat</sub><sup>-1</sup>·h<sup>-1</sup>, about eight times higher than that of [ZnCr&Z5]. DED manipulates ZnCr engine for methanol formation and drives FeMn engine for light olefins generation together, and then the formed methanol and light olefins are coordinately converted in situ into p-X-rich aromatics over Z5@SiO<sub>2</sub>. The DED model boosts the driving force for syngas/CO<sub>2</sub> conversion, simultaneously concerting the cooperation of "dual-engine" for p-X generation, resulting in extremely high STY of p-X. This study achieves non-petroleum p-X production at industrial-relevant level and advances knowledge in designing innovative heterogeneous catalysts.

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Publication Details

Journal
Nature Communications
Published
2024-09-14
DOI
https://doi.org/10.1038/s41467-024-52482-4
Citations
19
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
2.23

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article

Dual-engine-driven realizing high-yield synthesis of Para-Xylene directly from CO2-containing syngas

Shengying Zhao, Yingluo He, Baizhang Zhang, Minghui Tan et al.
19 citations
Nature Communications
Catalytic Processes in Materials Science
2.23
article

Dual-engine-driven realizing high-yield synthesis of Para-Xylene directly from CO2-containing syngas

Shengying Zhao, Yingluo He, Baizhang Zhang, Minghui Tan, Noritatsu Tsubaki, Guohui Yang, Tao Zhang, Fei Chen, Yang Wang, Chengwei Wang, Jie Yao, Xuemei Wu, Weizhe Gao, Taiki Arakawa
article en
19 citations

Abstract

The direct synthesis of light aromatics, especially para-xylene (p-X), from syngas/CO<sub>2</sub> is drawing strong interest, but improving the space-time yield (STY) of p-X is a significant challenge. Here, a dynamic "dual-engine-driven" (DED) catalytic system is designed by combining two partners of ZnCr and FeMn (named "dual-engine") with Z5@SiO<sub>2</sub> capsule zeolite. The DED catalyst of 1.0%FeMn&[ZnCr&Z5@SiO<sub>2</sub>] shows an extremely higher p-X STY of 36.1 g<sub>p-x</sub>·k<sub>gcat</sub><sup>-1</sup>·h<sup>-1</sup>, about eight times higher than that of [ZnCr&Z5]. DED manipulates ZnCr engine for methanol formation and drives FeMn engine for light olefins generation together, and then the formed methanol and light olefins are coordinately converted in situ into p-X-rich aromatics over Z5@SiO<sub>2</sub>. The DED model boosts the driving force for syngas/CO<sub>2</sub> conversion, simultaneously concerting the cooperation of "dual-engine" for p-X generation, resulting in extremely high STY of p-X. This study achieves non-petroleum p-X production at industrial-relevant level and advances knowledge in designing innovative heterogeneous catalysts.

Nature CommunicationsVol. 15(1)
Dalian University of Technology (CN), Dalian University (CN), Institute of Coal Chemistry (CN), China University of Petroleum, East China (CN), University of Chinese Academy of Sciences (CN), University of Toyama (JP)
National Natural Science Foundation of China, Shanxi Scholarship Council of China, China Scholarship Council, Japan Society for the Promotion of Science
Openalex Percentile: Top 8%
Catalytic Processes in Materials Science
2.23
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