Optimization of Cu‐SSZ‐13 Zeolite for Selective Oxidation of Methane to Methanol

Abstract Methane, the primary component of natural gas, plays an increasingly crucial role in global energy production and chemical synthesis. The selective oxidation of methane to methanol using clean, economically viable oxidants represents an optimal strategy for its efficient utilization. Herein, Cu‐SSZ‐13 zeolite catalysts were synthesized via ion exchange. By optimizing the preparation conditions and adjusting the cationic sites on the support, Cu‐SSZ‐13 zeolites with a single active site were developed. This approach led to catalysts exhibiting high methane conversion rates and methanol selectivity. Temperature‐programmed reduction (TPR) characterization revealed that the key active species responsible for the catalyst's high methanol yield was a single Cu species displaced from the six‐membered ring to the elliptical cavity.

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Publication Details

Journal
Chemical Engineering & Technology
Published
2025-06-30
DOI
https://doi.org/10.1002/ceat.70069
Citations
1
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
0.52

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article

Optimization of Cu‐SSZ‐13 Zeolite for Selective Oxidation of Methane to Methanol

Xuan Xiao, Meng Zhao, Lanlan Sun, Xuesong Gu
1 citations
Chemical Engineering & Technology
Catalytic Processes in Materials Science
0.52
article

Optimization of Cu‐SSZ‐13 Zeolite for Selective Oxidation of Methane to Methanol

Xuan Xiao, Meng Zhao, Lanlan Sun, Xuesong Gu
article en
1 citations

Abstract

Abstract Methane, the primary component of natural gas, plays an increasingly crucial role in global energy production and chemical synthesis. The selective oxidation of methane to methanol using clean, economically viable oxidants represents an optimal strategy for its efficient utilization. Herein, Cu‐SSZ‐13 zeolite catalysts were synthesized via ion exchange. By optimizing the preparation conditions and adjusting the cationic sites on the support, Cu‐SSZ‐13 zeolites with a single active site were developed. This approach led to catalysts exhibiting high methane conversion rates and methanol selectivity. Temperature‐programmed reduction (TPR) characterization revealed that the key active species responsible for the catalyst's high methanol yield was a single Cu species displaced from the six‐membered ring to the elliptical cavity.

Chemical Engineering & TechnologyVol. 48(7)
Tianjin University of Commerce (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 37%
Catalytic Processes in Materials Science
0.52
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