David Murindababisha , Abubakar Yusuf , Kien-Woh Kow , Yong Sun , Run Pan , Yong Ren , George Zheng Chen , Jianrong Li , Chengjun Wang , Jun He
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引用次数: 0
Abstract
Toluene, a volatile organic compound (VOC), poses significant environmental and health risks, necessitating efficient abatement technologies. This study explores the catalytic oxidation of toluene using CeO2-supported MIL-101(Fe) metal-organic frameworks (MOFs). A series of CeO2@MIL-101(Fe) catalysts with varying Ce loadings were synthesized and characterized through XRD, BET, XPS, SEM-EDS, HRTEM, H2-TPR, and in situ DRIFTS analyses. Among the synthesized materials, 6 % CeO2@MIL-101(Fe) exhibited superior catalytic performance, achieving 90 % toluene conversion (T90) at 239 °C, alongside remarkable stability over 60 hours. The catalyst demonstrated high tolerance to water vapor and sulfur dioxide (SO2), with full activity recovery after inhibitor removal. In situ DRIFTS and PTR-MS provided insights into the reaction mechanism, indicating that lattice oxygen plays a crucial role in toluene activation. The synergistic interaction between CeO2 and MIL-101(Fe) enhances redox properties and oxygen mobility, improving catalytic efficiency. These findings offer valuable insights into designing robust, MOF-based catalysts for VOC removal, providing a promising approach to mitigating air pollution.
期刊介绍:
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