Co‐Feeding CO<sub>2</sub> for Methylfuran Aromatization over Bifunctional Zeolite‐Supported ZnMoO<sub>4</sub>

Abstract Aromatization of biofuran offers promising approaches for sustainable biochemical production. However, this process is often hampered by low yields and severe coking on traditional zeolite catalysts. Herein, we report co‐feeding CO 2 for 2‐methylfuran (MF) aromatization (CCMA) over bifunctional ZSM‐5 supported ZnMoO 4 . This bifunctional catalyst can achieve both MF and CO 2 conversions of &gt;97 %, generating &gt;85 % carbon yield of target arenes and CO with negligible alkenes (0.05 %). Meanwhile, coke formation is remarkably suppressed from 22.3 % to 8.6 %. ZnMoO 4 /ZSM‐5 is capable of selectively manipulating the reaction intermediates and pathways of the CCMA reactions, favoring the cyclopentenones‐ and alkenes‐based dehydro‐aromatization rather than the benzofurans‐based pathway. This finding challenges the prevailing understanding that MF aromatization follows a hydrocarbon pool mechanism. Moreover, the abundant surface oxygen vacancies of ZnMoO 4 facilitate the adsorption of CO 2 and its subsequent reaction with coke. These insights into reaction mechanism and catalyst design for co‐conversion of CO 2 and biofuran can offer guidelines for process intensification in biomass utilization with a carbon‐negative manner.

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Publication Details

Journal
Angewandte Chemie
Published
2024-11-11
DOI
https://doi.org/10.1002/ange.202420779
Primary Topic
Zeolite Catalysis and Synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Co‐Feeding CO2 for Methylfuran Aromatization over Bifunctional Zeolite‐Supported ZnMoO4

Tongpo Yu, Shengpeng Xia, Anqing Zheng, Yunfei Gao et al.
Angewandte Chemie
Zeolite Catalysis and Synthesis
article

Co‐Feeding CO2 for Methylfuran Aromatization over Bifunctional Zeolite‐Supported ZnMoO4

Tongpo Yu, Shengpeng Xia, Anqing Zheng, Yunfei Gao, Xing Feng Zhu, Kun Zhao, Zhandong Wang, Hong Wang, Jinyang Zhang, Yuyang Fan, Zengli Zhao, Chenyang Wang
article en

Abstract

Abstract Aromatization of biofuran offers promising approaches for sustainable biochemical production. However, this process is often hampered by low yields and severe coking on traditional zeolite catalysts. Herein, we report co‐feeding CO 2 for 2‐methylfuran (MF) aromatization (CCMA) over bifunctional ZSM‐5 supported ZnMoO 4 . This bifunctional catalyst can achieve both MF and CO 2 conversions of &gt;97 %, generating &gt;85 % carbon yield of target arenes and CO with negligible alkenes (0.05 %). Meanwhile, coke formation is remarkably suppressed from 22.3 % to 8.6 %. ZnMoO 4 /ZSM‐5 is capable of selectively manipulating the reaction intermediates and pathways of the CCMA reactions, favoring the cyclopentenones‐ and alkenes‐based dehydro‐aromatization rather than the benzofurans‐based pathway. This finding challenges the prevailing understanding that MF aromatization follows a hydrocarbon pool mechanism. Moreover, the abundant surface oxygen vacancies of ZnMoO 4 facilitate the adsorption of CO 2 and its subsequent reaction with coke. These insights into reaction mechanism and catalyst design for co‐conversion of CO 2 and biofuran can offer guidelines for process intensification in biomass utilization with a carbon‐negative manner.

Angewandte ChemieVol. 137(11)
Kunming University of Science and Technology (CN), University of Science and Technology of China (CN), East China University of Science and Technology (CN), Chinese Academy of Sciences (CN), China Spallation Neutron Source (CN), Guangzhou Institute of Energy Conversion (CN), Institute of High Energy Physics (CN), National Synchrotron Radiation Laboratory (CN), Technical University of Munich (DE)
National Natural Science Foundation of China, National Key Research and Development Program of China, Chongqing Municipality Key Research and Development Program of China
Responsible consumption and production
Openalex Percentile: Top 84%
Zeolite Catalysis and Synthesis
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