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OXIDATION CATALYSIS OVER THE NANO-SUPPORTED METAL OXIDE CATALYSTS

机译:纳米支撑的金属氧化物催化剂上的氧化催化

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Nanoscale supported metal oxide catalysts were synthesized by hydrothermal method using γ-Al2O3 TiO2, ZrO2 and CeO2 as the supports, and impregnated 5% of V2O5, MoO3, and CrO3 on each supports. The physical properties and structural information were characterized by TEM, BET, XRD, EDS and in situ Raman spectroscopy. Raman results have revealed that the desired molecular arrangements of the active surface metal oxide phases have been achieved. The reactivity/selectivity properties of the nano- catalysts are chemically probed with steady-state catalytic studies of propane oxidative dehydrogenation and methanol oxidation reactions. The results of methanol oxidation reaction have indicated that there are redox sites and acid sites on the surface of the MoO_x/Al2O3 and VO_x/Al2O3catalysts, and only redox sites on the surface of the other catalysts. The results of propane oxidation reaction have revealed that the nano-supported chromia catalyst possesses the highest activity, however, the selectivity of propene decreases with increasing reaction temperature. The nano-supported vanadia catalyst possesses the lower activity and higher selectivity. In addition, 5% VO_x/ZrO2 remains the high selectivity under high reaction temperature of 550°C.
机译:通过使用γ-Al2O3 TiO2,ZrO2和CeO 2作为载体的水热法合成纳米级支持的金属氧化物催化剂,并在每个支撑体上浸渍5%的V2O5,MOO3和CRO 3。 TEM,BET,XRD,EDS和原位拉曼光谱特征在于物理性质和结构信息。拉曼结果表明,已经实现了活性表面金属氧化物相的所需分子布置。纳米催化剂的反应性/选择性特性用丙烷氧化脱氢和甲醇氧化反应的稳态催化研究进行了化学探测。甲醇氧化反应的结果表明,MOO_X / AL2O3和VO_X / AL2O3催化剂的表面上存在氧化还原位点和酸位点,并且仅在其他催化剂表面上的氧化还原位点。丙烷氧化反应的结果表明,纳米负载的染色催化剂具有最高的活性,然而,丙烯的选择性随着反应温度的增加而降低。纳米支撑的钒催化剂具有较低的活性和更高的选择性。此外,5%VO_X / ZrO2在550℃的高反应温度下保持高选择性。

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