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Volume 44 Issue 10
Oct.  2026
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Article Contents
ZHAO Danya, CHENG Yue, NIU Xinyu, GUO Jing, ZHOU Jiti, ZHAO Ling. Synergistic purification performance of NiMnAlO/ZSM-5 catalyst for NO and ethyl acetate[J]. ENVIRONMENTAL ENGINEERING , 2026, 44(10): 143-154. doi: 10.13205/j.hjgc.202610015
Citation: ZHAO Danya, CHENG Yue, NIU Xinyu, GUO Jing, ZHOU Jiti, ZHAO Ling. Synergistic purification performance of NiMnAlO/ZSM-5 catalyst for NO and ethyl acetate[J]. ENVIRONMENTAL ENGINEERING , 2026, 44(10): 143-154. doi: 10.13205/j.hjgc.202610015

Synergistic purification performance of NiMnAlO/ZSM-5 catalyst for NO and ethyl acetate

doi: 10.13205/j.hjgc.202610015
  • Received Date: 2026-07-20
    Available Online: 2026-11-10
  • To address the challenges associated with the synergistic removal of NOx and volatile organic compounds (VOCs) from industrial exhaust gases, including the mismatch between reaction requirements and the lack of multifunctional catalysts, a bifunctional Ni1Mn5AlO/ZSM-5 catalyst was prepared by integrating NiMnAlO oxide with ZSM-5 zeolite. With CO as the reducing agent and ethyl acetate as a model VOC, the catalytic performance of the composite was evaluated in a coupled system integrating CO-SCR and VOCs catalytic oxidation. The results demonstrated that the Ni1Mn5AlO/ZSM-5 catalyst exhibited superior NO reduction and ethyl acetate oxidation activities compared with pristine Ni1Mn5AlO and ZSM-5. By optimizing the Si/Al ratio of ZSM-5, the Ni1Mn5AlO/ZSM-5(Si/Al ratio=41.7) catalyst achieved the best overall catalytic performance, delivering an NO conversion rate of 71.6% at 350 ℃ and a T90 of 216 ℃ for ethyl acetate oxidation in a mixed atmosphere containing CO, NO, ethyl acetate, and O2. Characterization results indicated that the composite catalyst exhibited a microporous-mesoporous structure, and the number of acidic sites on the catalyst surface was significantly enhanced. Meanwhile, the ZSM-5 support regulated the electronic structure of Ni and Mn species, promoted the formation of Mn3+ active species, and optimized the balance between surface oxygen species and oxygen vacancies, thereby enhancing the redox capability of the catalyst. Kinetic analysis and in situ FTIR results indicated that CO acted as a reducing agent in the CO-SCR process to promote NO conversion while maintaining the surface redox cycle of the catalyst. Ethyl acetate was activated on acidi sites and subsequently oxidized through oxygen-containing intermediates, enabling the synergistic removal of NO and VOCs. This study provides new insights into the design of bifunctional catalysts for the simultaneous purification of multiple pollutants in complex industrial exhaust gases.
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