4.7 Article

Fabricating M/Al2O3/cordierite (M = Cr, Mn, Fe, Co, Ni and Cu) monolithic catalysts for ethyl acetate efficient oxidation: Unveiling the role of water vapor and reaction mechanism

期刊

FUEL
卷 303, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2021.121244

关键词

Monolithic catalysts; Transition metals oxides; Ethyl acetate oxidation; Effect of H2O; Reaction mechanism

资金

  1. National Natural Science Foundation of China [21876139, 21922606]
  2. Key R&D Program of Shaanxi Province [2019SF-244, 2019ZDLSF05-05-02]
  3. Shaanxi Natural Science Fundamental Shaanxi Coal Chemical Joint Fund [2019JLM-14]
  4. K. C. Wong Education Foundation
  5. Instrument Analysis Center of Xi'an Jiaotong University

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This study focused on the reduction and control of anthropogenic VOCs, with a particular emphasis on the fabrication of noble-metal-free monolithic catalysts for industrial VOC removal. A Mn-based cordierite monolithic catalyst showed exceptional activity and stability in the catalytic oxidation of ethyl acetate, with the presence of low levels of water vapor promoting EA conversion while higher concentrations inhibited it. This work provides important insights for designing VOC oxidation catalysts under practical conditions.
The reduction and control of VOCs from anthropogenic sources becomes a research hotspot due to their tremendous environment hazards. Fabricating efficient and applicable noble-metal-free monolithic catalysts is still a great challenge for industrial VOC economical removal. In this work, cordierite-based honeycomb monolithic catalysts (M/Al2O3/COR; M = Cr, Mn, Fe, Co, Ni and Cu) were synthesized by a versatile and scalable wash-coating method and adopted for ethyl acetate (EA) catalytic oxidation. Mn/Al2O3/COR possesses remarkable activity with 90% of ethyl acetate (EA) oxidized at 236 degrees C owing to abundant surface active oxygen species. Moreover, excellent stability and water resistance of Mn/Al2O3/COR were observed during long-term successive reaction. In situ DRIFTS results reveal that the decomposition of EA to ethanol is the main pathway under humid conditions, and the presence of low content water vapor (<= 1 vol%) promotes EA conversion ascribed to the presence of abundant OH derived from H2O dissociation; however, further increasing of water concentration inhibits EA conversion. The adsorption of OH over oxygen vacancies inhibits the generation of surface oxygen species and blocks further oxidation of intermediates to form acetate, leading to the reduction of CO2 yield and formation of coke aggregates. This work will provide instructive and feasible references for designing of VOC oxidation catalysts under practical reaction conditions.

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