Selective catalytic reduction of NOx by ammonia over phosphate-containing Ce0.75Zr0.25O2 solids

A zirconium phosphate @ Ce 0.75 Zr 0.25 O 2 (ZP/CZ) catalyst was synthesized by impregnating zirconium phosphates on Ce 0.75 Zr 0.25 O 2 microspheres. Catalysts with different structures were also synthesized by various methods to illustrate the structure advantage of ZP/CZ catalyst in selective catalytic reduction of NO x by ammonia (NH 3 -SCR). The catalysts were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), BET surface area, Infrared (IR) spectra, Ultraviolet-visible (UV–vis) spectroscopy, X-ray photoelectron spectroscopy (XPS), H 2 -temperature programmed reduction (TPR) and diffuse reflectance infrared Fourier transformed spectra (DRIFTS) of NH 3 /NO x adsorption. ZP/CZ catalyst presents excellent catalytic activity at 250–450   °C with a good N 2 selectivity under high space velocity of 300,000   h −1 . Firstly, the zirconium phosphate provides adsorption sites for ammonia on the surface of the catalyst and the cerium sites in the core act as the redox sites for NO oxidation. The pre-combination of zirconium and phosphate can reduce the strong interactions between phosphates and cerium ions. Therefore, the mobility of surface lattice oxygen on Ce 0.75 Zr 0.25 O 2 catalyst is retained, which is essential to obtain a catalyst with high NH 3 -SCR activity at low temperatures. Moreover, NH 4 NO 3 has proved to be an important intermediate for the NH 3 -SCR reaction on the surface of ceria based catalysts. The ZP/CZ catalyst preserves plenty of oxygen vacancies, facilitating the Ce 4+   →   Ce 3+ redox circles and therefore promotes the nitrites/nitrates formation and desorption on catalyst. Two distinct adsorption sites for NH 3 and NO x result in a close contact between ads-NH 3 /NH 4 + and ads-NO 3 − /NO 2 − species on ZP/CZ catalyst, which can react with NO rapidly with the participation of active surface lattice oxygen.