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Kinetics of Nitriding Fe-2 Wt Pct V Alloy: Mobile and Immobile Excess Nitrogen

机译:Fe-2 Wt Pct V合金渗氮动力学:流动和不流动的过量氮

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The kinetics of nitriding of Fe-2 wt pct V alloy was investigated as a function of time and temperature by exposing the alloy to a gas mixture of ammonia and hydrogen at constant nitriding potential 0.103 atm?1/2 at different nitriding temperatures, 520 °C, 550 °C, 580 °C, and 600 °C, for times up to 10, 10, 10, and 7 hours, respectively. The nitrided zone contains finely dispersed small vanadium-nitride precipitates in ferrite (α-Fe) grains. The nitrogen content within the nitrided zone is larger than expected on the basis of the vanadium content and the solubility of nitrogen in (stress-free) ferrite: excess nitrogen occurs. A model was developed that adequately predicts the evolution of the nitrogen concentration-depth profile of the nitrided layer. The model distinguishes quantitatively between the effects of mobile and immobile excess nitrogen, where immobile excess nitrogen is nitrogen adsorbed at the nitride platelet/matrix interface and mobile excess nitrogen is nitrogen dissolved in the matrix. The model has, as important (fit) parameters, the composition of the precipitated vanadium nitride, the effective diffusivity of nitrogen in the ferrite matrix surrounding the precipitates, and the solubility product of dissolved vanadium and dissolved nitrogen in the ferrite matrix. Analysis of the concentration-depth profile data at various nitriding temperatures exhibited the effect of the nitriding temperature on the amounts of mobile and immobile excess nitrogen.
机译:通过将Fe-2 wt pct V合金在不同氮化条件下暴露于恒定氮化电位为0.103 atm?1/2 的氨气和氢气的混合气体中,研究了其随时间和温度变化的动力学。温度520°C,550°C,580°C和600°C,分别长达10、10、10和7小时。渗氮区在铁素体(α-Fe)晶粒中包含细分散的小的氮化钒钒沉淀物。基于钒含量和氮在(无应力)铁素体中的溶解度,氮化区内的氮含量比预期的要大:会发生过量的氮。建立了一个模型,该模型可以充分预测氮化层的氮浓度-深度分布图的演变。该模型从数量上区分了流动的和不流动的过量氮的影响,其中流动的过量氮是吸附在氮化物血小板/基质界面的氮,而流动的过量氮是溶解在基质中的氮。该模型具有重要的(拟合)参数,包括沉淀的氮化钒的成分,氮在沉淀周围的铁素体基体中的有效扩散系数以及溶解的钒和溶解的氮在铁素体基体中的溶解度乘积。在各种氮化温度下对浓度-深度分布数据的分析显示出氮化温度对可移动和不可移动的过量氮量的影响。

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