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High-Temperature Oxidation of Zircaloy-4 in Oxygen-Nitrogen Mixtures

机译:氧化锆 - 4中的高温氧化在氧氮气混合物中

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Isothermal oxidation experiments with cladding tube segments of Zircaloy-4 (Zr-1.3%Sn) in oxygen-nitrogen model mixtures were performed at 800, 1000, and 1200 A degrees C for 6, 1 h, and 15 min, respectively. The gas compositions varied between 0 and 100 vol% nitrogen including 1 and 99 vol%. A strong accelerating effect of nitrogen on the oxidation kinetics was seen for a wide range of boundary conditions. At 800 A degrees C, oxidation in all mixtures with 1-99 % nitrogen resulted in higher reaction rates compared to the pure gases, especially after transition from protective to non-protective oxide scales. At 1000 and 1200 A degrees C, only starvation of oxygen in mixtures with low oxygen contents resulted in lower rates compared to pure oxygen. The oxide scales formed in the mixtures were very porous due to the formation of zirconium nitride at the metal-oxide interface and its oxidation during continuing reaction. The extension of the oxide-nitride zone increased with temperature and with nitrogen content in the gas mixture. Nitrogen seems also to affect the pre-transition reaction kinetics. The mechanism of the faster oxidation kinetics of zirconium alloys in atmospheres containing nitrogen will be discussed in this paper.
机译:用氧化氮素模型混合物中的锆铝-4(Zr-1.3%Sn)的离子氧化实验分别在800,10和1200℃下进行6,1 h和15分钟进行。气体组合物在0至100体积%的氮气之间变化,包括1和99体积%。在广泛的边界条件下观察到氮气对氧化动力学的强烈加速效果。在800℃下,与纯气体相比,含有1-99%氮的所有混合物中的氧化导致较高的反应速率,特别是在从保护性氧化物鳞片转变后过渡。在1000和1200℃下,与纯氧相比,仅具有低氧含量的混合物中的氧气中的氧气导致较低的速率。由于在延续反应期间形成在金属氧化物界面处的氮化锆及其氧化,在混合物中形成的氧化物鳞片非常多孔。氧化物 - 氮化物区的延伸随温度和气体混合物中的氮含量增加。氮似乎也影响预过渡预反应动力学。本文将讨论含氮含氮大气中锆合金氧化动力学的机制。

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