Modification of Cu/ZSM-5 catalyst with CeO_2 for selective catalytic reduction of NO_x with ammonia

来源 :Journal of Rare Earths | 被引量 : 0次 | 上传用户:merry_leaf
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Cu/ZSM-5 and CeO_2-modified Cu/ZSM-5 catalysts were prepared by a wetness impregnation method. The addition of CeO_2 was found to enhance the NO_x selective catalytic reduction(SCR) activity of the catalyst at low temperatures, but the high-temperature activity was weakened. The catalysts were characterized by X-ray diffraction(XRD), nitrogen physisorption, inductively coupled plasma optical emission spectrometry(ICP-OES), X-ray photoelectron spectroscopy(XPS), electron paramagnetic resonance(EPR), H_2 temperature-programmed reduction(TPR) and NH_3 temperature-programmed desorption(TPD). The results showed that more CuO clusters instead of isolated Cu~(2+) species were obtained on the modified catalyst. These active CuO clusters, as well as the Cu-Ce synergistic effect, improved the redox property of the catalyst and low-temperatures SCR activity via promoting the oxidation of NO to NO_2 and fast SCR reaction. The loss in high-temperatures activity was attributed to the enhanced competitive oxidation of NH_3 by O_2 and decreased surface acidity of the catalyst. Cu / ZSM-5 and CeO 2 -modified Cu / ZSM-5 catalysts were prepared by a wetness impregnation method. The addition of CeO 2 was found to enhance the NO_x selective catalytic reduction (SCR) activity of the catalyst at low temperatures, but the high -temperature activity was weakened. The catalysts were characterized by X-ray diffraction (XRD), nitrogen physisorption, inductively coupled plasma optical emission spectrometry (ICP-OES), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance H_2 temperature-programmed reduction (TPR) and NH_3 temperature-programmed desorption (TPD). These results showed that more CuO clusters instead of isolated Cu ~ (2+) species were obtained on the modified catalyst. These active CuO clusters, as well as the Cu-Ce synergistic effect, improved the redox property of the catalyst and low-SCR activity via promoting the oxidation of NO to NO 2 and fast SCR reaction. The loss in high-temperatures activity was attributed to the enhanced competitor itive oxidation of NH_3 by O_2 and decreased surface acidity of the catalyst.
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