Promoting the Catalytic Ozonation of Toluene by Introducing SO4~(2-) into the α-MnO2/ZSM-5 Catalyst to Tune Both Oxygen Vacancies and Acid Sites

摘要

Mn-based catalysts hold the promise of practical applications in catalytic ozonation of toluene at room temperature, yet improvement of toluene conversion and CO., selectivity remains challenging. Here, an innovative α-MnO2/ZSM-S catalyst modified with SO4~(2-) was successfully prepared, and both characterizations and density functional theory (DFT) calculations showed that SO4~(2-) introduction facilitated the formation of oxygen vacancies, Lewis and Bronsted acid sites, and active oxygen species and enhanced the adsorption ability of toluene on α-MnO2/ZSM- 5. Characterizations also showed that SO4~(2-) introduction made the catalyst possess larger specific surface area, superior reducibility, and stronger surface acidity. As a result, α-MnO2/ZSM-5 with a S/ Mn molar ratio of 0.019 exhibited the best toluene conversion and COx selectivity, 87 and 94, respectively, after the reaction for 8 h at 30 °C under an initial concentration of 5 ppm toluene and 45 ppm ozone, relative humidity of 45, and space velocity of 32,000 h~(-1), far superior to those of non-noble catalysts reported to date under comparable reaction conditions. The synergistic role of increased oxygen vacancies and acid sites of α-MnO2/ZSM-5 modified with SO4~(2-) resulted in excellent toluene conversion and COx selectivity. The findings represented a critical step toward the rational design and synthesis of highly efficient catalysts for catalytic ozonation of toluene.