摘要：Cerium‐based catalysts are very attractive for the catalytic abatement of nitrogen oxides(NOx)emitted from stationary ***,the main challenge is still achieving satisfactory catalytic activity in the low‐temperature range and tolerance to SO2 *** the present work,two series of Mo‐modified CeO_(2)catalysts were respectively obtained through a wet impregnation method(Mo‐CeO_(2))and a co‐precipitation method(MoCe‐cp),and the roles of the Mo species were systematically *** tests showed that the Mo‐CeO_(2)catalyst displayed much higher NO conversion at low temperature and anti‐SO2 ability than MoCe‐*** optimal Mo‐CeO_(2)catalyst displayed over 80%NO elimination efficiency even at 150°C and remarkable SO2 resistance at 250°C(nearly no activity loss after 40 h test).The characterization results indicated that the introduced Mo species were highly dispersed on the Mo‐CeO_(2)catalyst surface,thereby providing more Brønsted acid sites and inhibiting the formation of stable adsorbed NOx *** factors synergistically promote the selective catalytic reduction(SCR)reaction in accordance with the Eley‐Rideal(E‐R)reaction path on the Mo‐CeO_(2)***,the molybdenum surface could protect CeO_(2)from SO2 poisoning;thus,the reducibility of the Mo‐CeO_(2)catalyst declined slightly to an adequate level after *** results in this work indicate that surface modification with Mo species may be a simple method of developing highly efficient cerium‐based SCR catalysts with superior SO2 durability.

摘要：In this study,a trifunctional strategy was developed to prepare a confined Ni-based catalyst(Ni-CeO_(2)@SiO_(2))for dry reforming of methane(DRM)of two main greenhouse gases-CO_(2)and CH_(4).The Ni-CeO_(2)@SiO_(2)catalyst was fabricated by utilizing the confinement effect of the SiO_(2)shell and the synergistic interaction between Ni-Ce and the decoking effect of CeO_(2).The catalysts were systematically characterized via X-ray diffraction,N_(2 )adsorption/desorption,transmission electron microscopy,energy dispersive X-ray spectroscopy,hydrogen temperature reduction and desorption set by program,oxygen temperature program desorption,Raman spectroscopy,thermogravimetric analysis,and in situ diffuse reflectance infrared Fourier transform spectroscopy measurements to reveal their physicochemical properties and reaction *** Ni-CeO_(2)@SiO_(2)catalyst exhibited higher activity and stability than the catalyst synthesized via the traditional impregnation *** addition,no carbon deposition was detected over Ni-CeO_(2)@SiO_(2)after a 100 h durability test at 800℃,and the average particle size of Ni nanoparticles(NPs)in the catalyst increased from 5.01 to 5.77 ***,Ni-CeO_(2)@SiO_(2)also exhibited superior low-temperature stability;no coke deposition was observed when the catalyst was reacted at 600℃ for 20 *** high coking and sintering resistance of this confined Ni-based DRM catalyst can be attributed to its trifunctional *** trifunctional strategy developed in this study could be used as a guideline to design other high-performance catalysts for CO_(2)and CH4 dry forming and accelerate their industrialization.