首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Modification of surface and catalytic properties of Fe_2O_3 due to doping with rare-earth oxides Sm_2O_3 and Y_2O_3
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Modification of surface and catalytic properties of Fe_2O_3 due to doping with rare-earth oxides Sm_2O_3 and Y_2O_3

机译:稀土氧化物Sm_2O_3和Y_2O_3掺杂对Fe_2O_3表面和催化性能的改性

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The effects of Sm_2O_3 and Y_2O_33 doping of Fe_2O_3 on its surface and catalytic properties were investigated using nitrogen adsorption at -196 deg C,oxidation of CO by O_2 at 225-275 deg C and decomposition of H2O2 at 30-50 deg C.Fe_2O_3 was prepared by thermal decomposition of ferric carbonate at 350 deg C.The treated ferric oxide solid was prepared by wet impregnation method using finely powdered Fe2(CO_3)_3 solid followed by doping with different amounts of samarium nitrate or yttrium nitrate.Pure and doped Fe_2O_3 solids were calcined at 350-650 deg C.The extent of dopant added was varied between 1.0 and 6.0mol%.The results obtained revealed that doping of Fe_2O_3 solids with different amounts of Sm_2O_3 and Y_2O_3 decreased the degree of crystallinity and particle size of Fe_2O_3 phase.This doping process led to a progressive increase in the specific surface area of the treated Fe_2O_3 solids to an extent proportional to the amount of Sm_2O_3 and Y_2O_3 added.The doping process led also to a progressive increase in the catalytic activities of the investigated solids towards CO oxidation by O_2 and H_2O_2 decomposition.Also,the doping process did not modify the mechanism of the catalytic reactions but increased the concentration of catalytically active sites involved in the catalyzed reactions.
机译:研究了Fe_2O_3的Sm_2O_3和Y_2O_33掺杂对Fe_2O_3表面和催化性能的影响,方法是在-196℃吸附氮,在225-275℃用O_2氧化CO,在30-50℃用H2O2分解。Fe_2O_3为通过在350℃下热分解碳酸铁而制备。处理后的三氧化二铁固体是通过湿法浸渍法制备的,使用的是细粉状的Fe2(CO_3)_3固体,然后掺杂不同量的硝酸P或硝酸钇。纯净和掺杂的Fe_2O_3固体在350-650摄氏度下煅烧。添加的掺杂剂量在1.0至6.0mol%之间变化。结果表明,掺杂不同量Sm_2O_3和Y_2O_3的Fe_2O_3固体降低了Fe_2O_3相的结晶度和粒度。这种掺杂过程导致处理后的Fe_2O_3固体的比表面积逐渐增加,达到与Sm_2O_3和Y_2O_3添加量成比例的程度。还导致所研究的固体通过O_2和H_2O_2分解而对CO氧化的催化活性逐渐提高。此外,掺杂过程并未改变催化反应的机理,但增加了催化反应中涉及的催化活性位点的浓度。 。

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