Selective catalytic reduction (SCR) in the presence of NH 3 with different NO 2 /NO x ratios over activated carbon (AC) was investigated. NO x conversion at NO 2 /NO x = 1.0 was higher than that at NO 2 /NO x = 0 and 0.5 in the temperature range of 90−210 °C. NO 2 was easily reduced to NO over AC, resulting in a steadystate NO 2 /NO x ratio in the NO 2 −NH 3 SCR process, which is smaller than the feed NO 2 /NO x ratio set to 1.0. The results manifested that NH 4 NO 3 was deposited on AC when the temperature was lower than 150 °C. When the reaction temperature was higher than or equal to 150 °C, no NH 4 NO 3 deposition occurred, and NO x conversion eventually reached a steady state. Steadystate NO x conversion increased with the reaction temperature, reaching a maximum of 79.5% at 210 °C. Transient reaction analysis results showed that NH 4 NO 3 could react with NO, and the reaction rate increased gradually with the increase in temperature. The results of in situ diffuse reflectance infrared Fourier-transform spectroscopy also indicated that NO could react with NH 4 + , confirming that NH 4 NO 3 was an important immediate during the NO 2 −NH 3 SCR process. The mechanism of NO 2 −NH 3 SCR could be summarized as a combination of NH 4 NO 3 formation from NH 3 and NO 2 and NH 4 NO 3 consumption by NO and C(*). This study developed a systematic mechanism of NO 2 −NH 3 SCR over AC and provided a basis for AC-based catalysts at low temperatures for NO x removal.