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Novel CH(4) combustion catalysts derived from Cu-Co/X-Al (X = Fe, Mn, La, Ce) hydrotalcite-like compounds

机译:衍生自Cu-Co / X-Al(X = Fe,Mn,La,Ce)类水滑石化合物的新型CH(4)燃烧催化剂

摘要

Novel Cu(1)Co(2)/X(0.2)Al(0.8) well-mixed oxides (where X = Fe, Mn, Ce, La) were synthesized by calcinations of corresponding hydrotalcite-like compounds at 800 degrees C for 4 h. Their catalytic performance for the methane combustion was investigated. The oxides and their precursors were characterized by X-ray diffraction (XRD), thermogravimetry-differential scanning calorimetry (TG-DSC), temperature programmed reduction (TPR), X-ray photoelectron spectroscopy (XPS), and N(2) adsorption/desorption techniques. The derived oxides are mainly of spinel and tenorite phase, with surface area of 10-30 m(2)/g, where new phase CeO(2) and LaCoO(3) are segregated in Ce- and La-containing oxides, respectively. The catalytic activities of the catalysts are related to the redox properties of the metal cations and the species in the surface. Incorporation of the Mn and Fe element is helpful to the reduction of the oxide catalysts, which may lead to the enhancement of the catalytic activity. Among the catalysts investigated, Cu(1)Co(2)/Mn(0.2)Al(0.8) gives the highest catalytic activity. Light-off and complete oxidation temperature was centered at about 374 and 496 T, respectively. The less active was Cu(1)Co(2)/Fe(0.2)Al(0.8). The intensities of surface oxygen species over Mn- and Fe-containing oxides are much higher than other catalysts, implying the higher activity of surface oxygen for the methane combustion.
机译:新型Cu(1)Co(2)/ X(0.2)Al(0.8)混合均匀的氧化物(其中X = Fe,Mn,Ce,La)是通过在800摄氏度下煅烧相应的水滑石状化合物4合成的H。研究了它们对甲烷燃烧的催化性能。通过X射线衍射(XRD),热重分析-差示扫描量热法(TG-DSC),程序升温还原(TPR),X射线光电子能谱(XPS)和N(2)吸附/表征了氧化物及其前体解吸技术。派生的氧化物主要是尖晶石相和球铁矿相,表面积为10-30 m(2)/ g,其中新相CeO(2)和LaCoO(3)分别隔离在含Ce和La的氧化物中。催化剂的催化活性与金属阳离子和表面物种的氧化还原性能有关。 Mn和Fe元素的加入有助于氧化物催化剂的还原,这可以导致催化活性的提高。在所研究的催化剂中,Cu(1)Co(2)/ Mn(0.2)Al(0.8)具有最高的催化活性。起燃温度和完全氧化温度分别位于大约374和496 T的中心。活性较低的是Cu(1)Co(2)/ Fe(0.2)Al(0.8)。含锰和铁的氧化物上的表面氧物种的强度比其他催化剂高得多,这意味着表面氧对甲烷燃烧的活性更高。

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