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The Process of Tungsten-Nitride Precipitation upon Nitriding Ferritic Fe- 0.5 at. W Alloy

机译:氮化物铁素体Fe- 0.5时钨氮化物沉淀的方法。%W合金

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The precipitation of tungsten nitride upon internal nitriding of ferritic Fe- 0.5 at.% W alloy was investigated at 610°C in a flowing NH3/H2 gas mixture. Different tungsten nitrides developed successively; the thermodynamically stable hexagonal 5-WN could not be detected. The state of deformation of the surface plays an important role for the development of tungsten nitride at the surface. The morphologies of the tungsten nitrides developed at the surface and those precipitated at some depth in the specimen are different. The nitride particles at the surface exhibit mostly an equiaxed morphology (with the size of the order 0.5 μm) and have a crystal structure which can be described as a superstructure derived from hexagonal 6-WN. These nitride particles show a strong preferred orientation with respect to the specimen frame of reference but have no relation with the crystal orientation of the surrounding ferrite matrix. In the bulk, nano-sized and finely dispersed platelet-like precipitates grow preferentially along {100}_(α_(Fe)). It is unclear whether these precipitates consist of binary iron nitride α"-Fe_(16)N_2 or of a ternary Fe-W-N. Additionally to the finely dispersed particles, bigger nitrides at ferrite grain boundaries develop exhibiting platelet-type morphology and possessing a crystal structure which can be also described as a superstructure derived from hexagonal 8-WN. Upon prolonged nitriding assumed discontinuous precipitation of the initially precipitated finely dispersed nitrides starts from the ferrite-grain boundaries resulting in lamellas consisting of alternate ferrite and hexagonal nitride lamellas, whereas the nitride lamellas having a Pitsch-Schrader orientation relationship with the surrounding ferrite matrix. The nitrides precipitated upon nitriding in the bulk were found to be unstable during H_2 reduction at 470°C. Remarkably, upon such low temperature dissolution of the nitrides took place but only the nitrogen from the nitride particles could diffuse out of the nitride platelets and the specimen, leaving W-rich regions (W-"clusters") at the location of the original precipitates.
机译:在氮化钨在内部氮化物的氮化钨氮化物在610℃下在流动的NH 3 / H 2气体混合物中进行沉淀。不同钨氮化物连续开发;无法检测到热力学稳定的六边形5-Wn。表面的变形状态对表面的钨氮化物的发展起着重要作用。在表面上发育的钨氮化物的形态和样品中某些深度沉淀的那些不同。表面处的氮化物颗粒主要是等轴形态(尺寸为0.5μm的尺寸)并且具有晶体结构,其可以描述为衍生自六边形6-Wn的上部结构。这些氮化物颗粒相对于样本参考框架显示出强的优选取向,但与周围铁氧体基质的晶体取向无关。在块状,纳米尺寸和精细分散的血小板状沉淀物沿{100} _(α_(Fe))优先生长。目前尚不清楚这些沉淀物是否由二元铁氮化物α“-fe_(16)N_2或三元Fe-Wn组成。另外,在铁素体晶界下的较大氮化物显现出血小板型形态并具有晶体也可以描述的结构作为衍生自六边形8-Wn的上部结构。在延长氮化的假设初始沉淀的细分分散的氮化物的延长氮化的不连续沉淀时,从铁氧体晶界开始,导致由交替的铁氧体和六边形氮化物覆盖物组成的薄片。具有与周围铁氧体基质的Pitsch-Schrader取向关系的氮化物薄片。在470℃的H_2降低期间发现在散装中沉淀的氮化物在470℃下进行不稳定。显着的情况下,在氮化物的这种低温溶解时发生但仅发生来自氮化物颗粒的氮可以扩散出氮化物血小板和试样,在原始沉淀物的位置留下富有的地区(W-“簇”)。

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