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In Situ Optical Studies of Oxidation Kinetics of Ni/YSZ Cermet Anodes

机译:Ni / YSZ Cermet阳极氧化动力学的原位光学研究

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Vibrational Raman spectroscopy was used to monitor directly and in situ the kinetics of nickel particle surface oxidation and reduction at 715°C and 550°C. Reduction with hydrogen happens in a matter of seconds, but surface oxidation requires 5-10 minutes to reach an asymptotic limit. Ni oxidation kinetics are explored for samples prepared with three different Ni particle sizes (5-20 nm, 2-3 μm, and 3-7 μm). Data show that initial particle size is not a significant factor in controlling the pseudo-first order oxidation rates. Furthermore, water vapor by itself does not appear to oxidize the Ni particles in contrast to reports. However, humitidity does affect the susceptibility of Ni to subsequent oxidation when the H_2O(g) is replaced with O_2(g). Following exposure to water, Ni oxidation appears to follow two separate 1st order kinetic processes. This effect occurs only for the first oxidation cycle following exposure to water.
机译:振动拉曼光谱用于直接监测,原位在715℃和550℃下进行镍颗粒表面氧化和还原的动力学。在几秒钟内发生氢气的减少,但表面氧化需要5-10分钟才能达到渐近极限。探索用三种不同的Ni粒径(5-20​​nm,2-3μm和3-7μm)制备的样品探索Ni氧化动力学。数据表明,初始粒度不是控制伪第一次氧化率的重要因素。此外,与报告相比,水蒸气本身并不氧化Ni颗粒。然而,当用O_2(g)代替H_2O(g)时,湿度会影响Ni对随后的氧化的敏感性。在暴露于水后,Ni氧化似乎遵循两个单独的第一阶动力学过程。这种效果仅发生在暴露于水后的第一氧化循环。

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