甲烷化
催化作用
可再生能源
沸石
碳纤维
环境科学
化学
废物管理
材料科学
化学工程
有机化学
复合数
工程类
电气工程
复合材料
作者
Chandran Rajendran,Mahshab Sheraz,Amornchai Arpornwichanop,Anh N. Phan,E. Parthiban,Phuet Prasertcharoensuk
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-10-03
卷期号:39 (41): 19574-19599
被引量:1
标识
DOI:10.1021/acs.energyfuels.5c03613
摘要
With rising CO2 emissions and the need for sustainable energy solutions, research into CO2 methanation has accelerated. This catalytic process converts CO2 to methane, a storable energy carrier with diverse applications. Zeolite-based catalysts have shown great promise for CO2 methanation due to their unique pore structures, thermal stability up to 400 °C, and ability to support metal dispersion. These properties make them well-suited for the selective and efficient production of methane. This review synthesizes recent progress in zeolite-catalyzed CO2 methanation. It thoroughly examines their structural properties and how different metal modifications affect their catalytic activity. While numerous reviews exist on CO2 methanation, this work offers a unique critical analysis by systematically comparing the catalytic performance of distinct zeolite frameworks: MFI (ZSM-5), BEA (Beta), and FAU (Y, X). This work critically evaluates how pore architecture, acidity, and ion-exchange capacity directly influence the activity, CH4 selectivity, and long-term stability of the final catalyst. By identifying key knowledge gaps and outlining a roadmap for the rational design of next-generation zeolite catalysts, this review provides a new perspective aimed at accelerating the transition from laboratory research to industrial application.
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