Highly Selective and Stable Hydrogenation of CO <sub>2</sub> /H <sub>2</sub> S to Methyl Mercaptan over a Synergistic Cu−Mo Catalyst

Selective hydrogenation of carbon dioxide (CO2) with hydrogen sulfide (H2S) to methyl mercaptan (CH3SH) offers a strategy for the simultaneous utilization of CO2 and H2S waste gases from chemical processes. However, achieving activation of the C=O bond while maintaining high CH3SH selectivity remains a challenge. In this study, we report a Cu-doped porous spherical KMoS2/SiO2 catalyst (4CuKMo/SiO2) that overcomes this challenge to afford selective CH3SH synthesis. Under optimized conditions (1.5 MPa, 320 °C), the catalyst achieves a CO2 conversion of 28% with 96% CH3SH selectivity. Furthermore, the catalytic activity remains stable with no sharp degradation over a continuous 160-h operation. Mechanistic studies reveal that the Cu doping promotes the formation of sulfur vacancies, which facilitate the adsorption and activation of both CO2 and H2S. In addition, the synergistic interaction between Cu and Mo species redirects the reaction pathway from the typical COS intermediate route to a thermodynamically favorable CH3OH-mediated pathway, thereby enhancing the selective formation of CH3SH.

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Publication Details

Journal
ACS Catalysis
Published
2026-04-22
DOI
https://doi.org/10.1021/acscatal.6c01142
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
0.00

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article

Highly Selective and Stable Hydrogenation of CO 2 /H 2 S to Methyl Mercaptan over a Synergistic Cu−Mo Catalyst

Shijing Liang, Ganchang Lei, Xiaohai Zheng, Hongping Yan et al.
ACS Catalysis
Carbon Dioxide Capture Technologies
article

Highly Selective and Stable Hydrogenation of CO 2 /H 2 S to Methyl Mercaptan over a Synergistic Cu−Mo Catalyst

Shijing Liang, Ganchang Lei, Xiaohai Zheng, Hongping Yan, Shiping Wang, Yingying Zhan, Lijuan Shen, Rui Huang, Lilong Jiang
article en

Abstract

Selective hydrogenation of carbon dioxide (CO2) with hydrogen sulfide (H2S) to methyl mercaptan (CH3SH) offers a strategy for the simultaneous utilization of CO2 and H2S waste gases from chemical processes. However, achieving activation of the C=O bond while maintaining high CH3SH selectivity remains a challenge. In this study, we report a Cu-doped porous spherical KMoS2/SiO2 catalyst (4CuKMo/SiO2) that overcomes this challenge to afford selective CH3SH synthesis. Under optimized conditions (1.5 MPa, 320 °C), the catalyst achieves a CO2 conversion of 28% with 96% CH3SH selectivity. Furthermore, the catalytic activity remains stable with no sharp degradation over a continuous 160-h operation. Mechanistic studies reveal that the Cu doping promotes the formation of sulfur vacancies, which facilitate the adsorption and activation of both CO2 and H2S. In addition, the synergistic interaction between Cu and Mo species redirects the reaction pathway from the typical COS intermediate route to a thermodynamically favorable CH3OH-mediated pathway, thereby enhancing the selective formation of CH3SH.

ACS Catalysis
Fujian Normal University (CN), State Key Laboratory of Pollution Control and Resource Reuse (CN), State Key Laboratory of Chemical Engineering (CN), Fuzhou University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Fujian Province, Science Fund for Distinguished Young Scholars of Fujian Province
Openalex Percentile: Top 12%
Carbon Dioxide Capture Technologies
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