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    WU Xueping, LIU Xiaoxue, SUN Xiaolin, WU Haifeng, CHEN Yazhong, ZHANG Xianlong, WEN Songying. Catalytic oxidation of formaldehyde at room temperature over MnOx/SFCCC catalyst: deactivation and regenerationJ. Journal of Chemical Engineering of Chinese Universities, 2026, 40(0): xx-xx. DOI: 10.3969/j.issn.1003-9015.2026-0018
    Citation: WU Xueping, LIU Xiaoxue, SUN Xiaolin, WU Haifeng, CHEN Yazhong, ZHANG Xianlong, WEN Songying. Catalytic oxidation of formaldehyde at room temperature over MnOx/SFCCC catalyst: deactivation and regenerationJ. Journal of Chemical Engineering of Chinese Universities, 2026, 40(0): xx-xx. DOI: 10.3969/j.issn.1003-9015.2026-0018

    Catalytic oxidation of formaldehyde at room temperature over MnOx/SFCCC catalyst: deactivation and regeneration

    • To address the deactivation of Mn-based catalysts during the catalytic oxidation of formaldehyde at room temperature, a MnOx/SFCCC catalyst was prepared via an in-situ growth method using spent fluid catalytic cracking catalyst (SFCCC) as the support. The causes of catalyst deactivation during continuous operation and the performance recovery after thermal regeneration at 50-250 °C were systematically investigated. Among the regeneration temperatures examined, the catalyst regenerated at 200 °C exhibited the best recovery performance, with its activity restored to 95% within 10 h. After four consecutive reaction–regeneration cycles, the formaldehyde removal efficiency still remained above 60%. BET and SEM results showed that the fresh catalyst possessed a specific surface area of 154 m2·g−1 and a pore volume of 0.191 cm3·g−1. After deactivation, small-particle agglomeration appeared on the catalyst surface, accompanied by a significant decrease in textural properties, with the specific surface area and pore volume dropping to 90 m2·g−1 and 0.141 cm3·g−1, respectively. After regeneration at 200 °C, these values recovered to 130 m2·g−1 and 0.185 cm3·g−1, respectively. XPS, O2-TPD, and H2-TPR analyses revealed that catalyst deactivation was associated with the reduction of Mn3+ species and the consumption of surface reducible oxygen species. FTIR, TPO, and TG further confirmed that the deactivation mainly resulted from the reversible coverage of active sites by carbon-containing intermediates, predominantly formate species, and that mild heating at 200 °C could effectively regenerate the catalyst.
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