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首页> 外文期刊>Journal de Physique, IV: Proceedings of International Conference >Texture analysis of oxide dispersion strengthened (ODS) Fe alloys by X-ray and neutron diffraction
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Texture analysis of oxide dispersion strengthened (ODS) Fe alloys by X-ray and neutron diffraction

机译:X射线和中子衍射分析弥散强化(ODS)铁合金的织构

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摘要

The ferritic ODS alloys studied were obtained by mechanical alloying. This strengthening method is very attractive, in particular for nuclear applications. In order to ensure the alloy a good compromise between mechanical resistance and ductility at high temperatures, it is necessary to control the microstructure and in particular the evolution during the recrystallization. First, a preliminary study, performed by X ray diffraction and optical microscopy, shows several grain growth mechanisms; in particular, the "abnormal" grain growth mechanism which conducts to a large grain size [1], [2]. After annealing (3600s at 1470 ℃), the 30% cold-worked (swaging) alloys exhibit an heterogeneous microstructure with a large grains size (~200 to 500 μm) in the heart and near the surface of the material when the intermediate zone is inhabited by small grains (~1 μm). For a higher cold-work level (60%), large size grains are only present in the periphery of the material. On account of the large grain size and strong heterogeneity of the microstructure, texture analysis using laboratory x-ray beam in not well adapted and so we have decided to use neutron beam. The neutron diffraction texture analysis has been performed at the Laboratoire Leon Brillouin on the 6T1 diffractometer on 2 different rods of the alloy (corresponding to the reduction ratios of 30% and 60%). Specific samples have been machined to characterise separately the zones with a different microstructure. After deformation, the alloys exhibit a typical α-fibre texture {hkl}<110>~ whatever the area of the sample and the reduction ratio. After recrystallization, a very inhomogeneous texture is evidenced through the thickness of the sample, in particular for the rod deformed with a reduction ratio of 30%: in the heart and in the periphery of the rod, a "single-crystal" type texture is observed; the α fibre remains for the intermediate diameter of the rod. For the rod cold rolled with a reduction ratio of 60%, the α-fibre keeps on the heart of the material and as in the precedent case, a "single-crystal" type texture is observed near the surface of the sample. EBSD measurements have been performed to explicit at explicit at a local scale this behaviour and in order to furnish some input data for the simulation of static recrystallization.
机译:通过机械合金化获得了研究的铁素体ODS合金。这种加强方法非常有吸引力,特别是对于核应用。为了确保合金在高温下的机械阻力和延展性之间的良好折衷,必须控制微观结构,特别是在重结晶过程中的发展。首先,通过X射线衍射和光学显微镜进行的初步研究显示了几种晶粒长大的机理。尤其是“异常”晶粒长大机制,可传导至大晶粒尺寸[1],[2]。经过退火处理(在1470℃下为3600s)后,当中间区位于中间时,30%的冷加工(锻造)合金在心脏和材料表面附近呈现出异质组织,晶粒尺寸较大(约200至500μm)。被小颗粒(〜1μm)占据。对于较高的冷加工水平(60%),大尺寸晶粒仅存在于材料的外围。由于大晶粒尺寸和微观结构的强烈异质性,使用实验室X射线束进行的纹理分析无法很好地适应,因此我们决定使用中子束。在实验室的Leon Brillouin实验室的6T1衍射仪上,对合金的2个不同棒进行了中子衍射织构分析(对应于30%和60%的还原率)。对特定样品进行了加工,以分别表征具有不同微观结构的区域。变形后,无论样品面积和压缩比如何,合金均表现出典型的α-纤维织构{hkl} <110>〜。重结晶后,通过样品的厚度可以证明非常不均匀的织构,特别是对于变形率降低30%的棒材:在棒材的心脏和外围,是“单晶”型织构观测到的; α纤维保留在棒的中间直径内。对于以60%的压下率进行冷轧的棒材,α纤维保留在材料的心脏上,与以前的情况一样,在样品表面附近观察到“单晶”型织构。 EBSD测量已被执行以在局部范围内显式地显露此行为,并为静态重结晶的模拟提供一些输入数据。

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