Generation of multi-valence CuxO by reduction with activated semi-coke and their collaboration in the selective reduction of NO with NH3

Multi-valence Cu x O has been demonstrated to have high activity in the low-temperature selective catalytic reduction of NO x with NH3 (NH3-SCR). Here, Cu x O was loaded onto activated semi-coke (ASC) for SCR, which has shown satisfactory low-temperature SCR activity. By virtue of the reduction property of carbon, the valence of Cu was regulated by simply adjusting the calcination temperature. The high concentration of Cu+ generated from the reduction of CuO by ASC during calcination can collaborate to form Cu2+/Cu+ circulation. After systematic characterization by XPS, H2-TPD, and NH3-TPR, it is revealed that abundant acidic sites and surface reactive oxygen species are formed on the surface of the catalysts. Further investigation with in situ DRIFTS confirms that the NH3-SCR over the as-prepared CuO|Cu2O-ASC catalysts simultaneously follows the Langmuir-Hinshelwood (L-H) and Eley-Rideal (E-R) pathways, attributed to the synergistic effects of Cu2+ and Cu+.