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首页> 外文期刊>International Journal of Quantum Chemistry >Surface properties and performance for VOCs combustion of LaFe1-yNiyO3 perovskite oxides
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Surface properties and performance for VOCs combustion of LaFe1-yNiyO3 perovskite oxides

机译:LaFe1-yNiyO3钙钛矿氧化物的挥发性有机化合物燃烧的表面性质和性能

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LaFeO3, LaNiO3 and substituted LaFe1-yNiyO3 (y = 0.1, 0.2 and 0.3) perovskites were synthesized by the citrate method and used in the catalytic combustion of ethanol and acetyl acetate. Chemical composition was determined by atomic absorption spectrometry (AAS) and specific areas from nitrogen adsorption isotherms. Structural details and surface properties were evaluated by temperature-programmed reduction (TPR), infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), temperature-programmed desorption of oxygen (O-2-TPD) and photoelectron spectroscopy (XPS). Characterization data revealed that total insertion of nickel in the LaFeO3 takes place for substitution y = 0.1. However, NiO segregation occurs to some extent, specifically at higher substitutions (y > 0.1). The catalytic performance of these perovskites was evaluated in the combustion of acetyl acetate and ethanol. Among these molecules, ethanol exhibited the lowest ignition temperature, and the catalytic activity expressed as intrinsic activity (mol m(-2) h(-1)) was found to increase substantially with the nickel substitution. These results can be explained in terms of the cooperative effect of a LaFe1-yNiyO3 and NiO phases, whose relative concentration determines the oxygen activation capability and hence their reactivity. (C) 2008 Elsevier Inc. All rights reserved.
机译:通过柠檬酸盐法合成了LaFeO3,LaNiO3和取代的LaFe1-yNiyO3(y = 0.1、0.2和0.3)钙钛矿,并用于乙醇和乙酸乙酰酯的催化燃烧。通过原子吸收光谱法(AAS)和氮吸附等温线的特定区域确定化学成分。结构细节和表面特性通过程序升温还原(TPR),红外光谱(FTIR),X射线衍射分析(XRD),程序升温的氧气脱附(O-2-TPD)和光电子能谱(XPS)进行评估。表征数据表明,镍在LaFeO3中的总插入取代量为y = 0.1。但是,NiO偏析在一定程度上发生,特别是在较高的取代度下(y> 0.1)。这些钙钛矿的催化性能在乙酰乙酸盐和乙醇的燃烧中进行了评估。在这些分子中,乙醇表现出最低的着火温度,并且发现以内在活性表示的催化活性(mol m(-2)h(-1))随着镍的取代而大大增加。这些结果可以用LaFe1-yNiyO3和NiO相的协同作用来解释,它们的相对浓度决定了氧的活化能力并因此决定了它们的反应性。 (C)2008 Elsevier Inc.保留所有权利。

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