Abstract

Mn/TiO2 catalysts with varying solid contents were innovatively prepared by the sol-gel method and were used for selective catalytic reduction of NO at low temperatures using NH3 (NH3-SCR) as the reducing agent. Surprisingly, it was found that as the solid content of the sol increased, the catalytic activity of the developed Mn/TiO2 catalyst gradually increased, showing excellent catalytic performance. Notably, the Mn/TiO2 (50%) catalyst demonstrates outstanding denitration performance, achieving a 96% NO conversion rate at 100 °C under a volume hourly space velocity (VHSV) of 24,000 h-1, while maintaining high N2 selectivity and stability. It was discovered that as the solid content increased, the catalyst's specific surface area (SSA), surface Mn4+ concentration, chemisorbed oxygen, chemisorption of NH3, and catalytic reducibility all improved, thereby enhancing the catalytic efficiency of NH3-SCR in degrading NO. Moreover, NH3 at the Lewis acidic sites and NH4+ at the Bronsted acidic sites of the catalyst were capable of reacting with NO. Conversely, NO and NO2 adsorbed on the catalyst, along with bidentate and monodentate nitrates, were unable to react with NH3 at low temperatures. Consequently, the developed catalyst's low-temperature catalytic reaction mechanism aligns with the E-R mechanism.

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