催化作用
甲醇
选择性
空间速度
化学工程
立方氧化锆
材料科学
无定形固体
产量(工程)
化学
无机化学
有机化学
冶金
陶瓷
工程类
作者
Amanda S. Mbhele,Mduduzi N. Cele,Mzamo L. Shozi,Holger B. Friedrich
标识
DOI:10.1016/j.sajce.2024.08.003
摘要
The rise in carbon dioxide concentration is a primary anthropogenic source of severe climate change and ecological issues. Catalytic hydrogenation of CO2 into value-added chemicals and fuels including methanol is one of the attractive environmentally friendly ways to valorize carbon-containing feedstock and reduce global CO2 emissions. However, enhancing catalytic activity to achieve high methanol yield and selectivity while maintaining stability remains a major challenge. This study investigated the promotion of Cu/MOF-5 catalysts with varying loadings of ZrO₂ to determine its effects on catalytic performance in CO₂ hydrogenation. The copper loading was kept constant while the ZrO₂ content on the MOF-5 support was varied via the impregnation method. The addition of ZrO₂ was found to influence the BET surface area, suggesting the presence of amorphous ZrO₂, as its crystalline phases were not detected in x-ray diffractograms. Catalytic results demonstrated that ZrO₂ addition enhanced the catalytic activity, with increased CO₂ conversion up to 13.2 %. The results showed a correlation between catalytic performance and the reducibility of the active metal, driven by the amount of ZrO₂ present. The catalyst with the highest ZrO₂ loading exhibited the best performance, attributed to its increased surface area and enhanced reducibility. Under optimized conditions (GHSV of 1350 h⁻¹, temperature of 200 °C, and pressure of 30 bar), the catalyst achieved 100 % methanol selectivity. This study underscores the significant role of ZrO₂ as a promoter in enhancing the activity and selectivity of Cu/MOF-5 catalysts, providing critical insights into the design of efficient catalytic systems for CO₂ hydrogenation.
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