TiO2/γ-Al2O3 supported In/Ag catalysts were prepared by impregnation method,and investigated for NO reduction with CO as the reducing agent under lean burn conditions.The microscopic structure and surface properties of the catalysts were studied by N2 adsorption-desorption,X-ray diffraction,transmission electron microscopy,X-ray photoelectron spectroscopy,ultraviolet-visible spectroscopy,H2 temperature-programmed reduction and Fourier transform infrared spectroscopy.TiO2/γ-Al2O3 supported In/Ag is a good catalyst for the reduction of NO to N2.It displayed high dispersion,large amounts of surface active components and high NO adsorption capacity,which gave good catalytic performance and stability for the reduction of NO with CO under lean burn conditions.The silver species stabilized and improved the dispersion of the indium species.The introduction of TiO2 into the γ-Al2O3 support promoted NO adsorption and improved the dispersion of the indium species and silver species.
采用等体积浸渍法制备了Pt/HBeta催化剂,并在10 mL固定床反应装置上评价了反应温度和质量空速对Pt/HBeta催化正己烷临氢异构化反应的影响,在此基础上建立正己烷异构化反应动力学模型。结果表明:在 240~ 260 ℃内正己烷临氢异构化反应可以用拟一级动力学模型来描述,反应的活化能 E a=139.06 kJ/mol,指前因子 A = 7.3814×10 13 h -1;建立了连串反应动力学模型,第一步反应活化能 E a1 =167.80 kJ/mol, A 1=7.2130×10 16 h -1 ,第二步反应活化能 E a2 =118.34 kJ/mol, A 2=1.3053×10 11 h -1;当反应温度大于260 ℃,拟一级动力学模型不再适合,修正后270 ℃时的反应级数为1.3,280 ℃时的反应级数为1.7。
This paper reports a sustainable,water-assisted,solid-state method for synthesizing ammonium nickel molybdate((NH4)HNi2(OH)2(MoO4)2,ANM),a precursor for an unsupported hydrodesulfurization(HDS) catalyst.The associated ANM formation mechanism is also discussed.The synthesis route consists of physical mixing of the raw materials,water-assisted grinding and heating.The formation mechanism involves replacement of a Mo atom by a Ni atom,generating the metastable intermediate(NH4)4(NiH6Mo6O(24))·5H2O.Heating of this intermediate at 120 ℃ removes the added water and produces ANM.Catalysts prepared by this method exhibit almost the same physicochemical properties and catalytic performance during the HDS of dibenzothiophene as materials made from ANM synthesized by a chemical precipitation procedure.Compared with traditional hydrothermal or chemical precipitation methods,this water-assisted,solid-state synthesis provides several significant advantages,including simplifying the synthetic procedure,reducing waste and energy costs and increasing product yields.These features will be highly important with regard to allowing the application of ANM in industrial-scale processes involving HDS reactions.This water-assisted,solid-state strategy can also be extended to the synthesis of isomorphous compounds such as ammonium cobalt(zinc and copper) molybdate.