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

机译:氮化铁素体Fe-0.5a​​t.W合金中氮化钨的析出过程

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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 NH_3/H_2 gas mixture. Different tungsten nitrides developed successively; the thermodynamically stable hexagonal δ-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 δ-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}a-Fe. It is unclear whether these precipitates consist of binary iron nitride a"-Fe16N2 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 δ-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 H2 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610°C的流动NH_3 / H_2气体混合物中研究了铁素体Fe-0.5 at。%W合金内部氮化时氮化钨的沉淀。不同的氮化钨相继发展。不能检测到热力学稳定的六角形δ-WN。表面的变形状态对于表面氮化钨的发展起重要作用。在表面形成的氮化钨的形态和在样品中一定深度处沉淀的氮化钨的形态是不同的。表面的氮化物颗粒主要表现出等轴形态(大小约为0.5μm),并且具有可以描述为源自六方δ-WN的超结构的晶体结构。这些氮化物颗粒相对于参考标本框架显示出强烈的首选方向,但与周围铁氧体基质的晶体方向无关。总体上,纳米尺寸且细分散的片状沉淀物优先沿{100} a-Fe生长。尚不清楚这些沉淀物是由二元氮化铁α“ -Fe16N2还是三元Fe-WN组成。除了细分散的颗粒外,在铁素体晶界处的较大氮化物还表现出片晶型形态并具有可在长时间的渗氮过程中,假设最初析出的细分散氮化物的不连续沉淀从铁素体-晶界开始,从而形成由交替的铁素体和六角形氮化物薄片组成的薄片,而氮化物薄片具有Pitsch-Schrader取向与周围的铁素体基体之间的关系,在470°C的H2还原过程中,氮化时在主体中氮化时析出的氮化物不稳定。氮化物颗粒可能会从氮化物薄片中扩散出来,并且样品,在原始沉淀物的位置留下富W的区域(W-“簇”)。

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