首页> 外文会议>International Conference on Diffusion, Segregation and Stresses in Materials, May 27-31, 2002, Moscow, Russia >The Effect of Deformation on Structure and Properties of Surface Diffusion Layers Formed in Iron Alloys under Alloying by Nitrogen and Carbon
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The Effect of Deformation on Structure and Properties of Surface Diffusion Layers Formed in Iron Alloys under Alloying by Nitrogen and Carbon

机译:氮碳共合金作用下变形对铁合金表面扩散层结构和性能的影响

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The influence of preliminary plastic deformation in the range of 5-70 % on the structure formation and mechanical properties of surface layers in iron-based alloys under diffusion alloying by nitrogen and carbon in ammonia and propane-butane gaseous environment at the temperature 853 K during 0.5-6 hours was studied. Surface diffusion layers were investigated by means of X-ray diffraction, microhardness and wear resistance tests. It was established that the surface layer of iron alloy after gas saturation by nitrogen and carbon consisted of ε -phase with the hexagonal closed packed crystal structure or θ - phase with the orthorhombic structure isostructural to cementite lattice and the solid solution of nitrogen and carbon in α -phase. The deformation within the range of 25-30 % substantially affects surface diffusion layer structure, phase and chemical composition and properties. The θ - phase was revealed in the layer after 25-30 % deformation and saturation in gas mixture of 90 % ammonia and 10 % propane-butane. Obtained in this way layers show maximum microhardness, wear resistance and thickness. The ε -phase was formed in the alloy after deformation out of the 25-30 % ranges. The lattice spacing of the α -phase containing nitrogen and carbon decreases non-linearly within the 25-40 % degree of plastic deformation. We assume that high strengthening of the surface layers results from interaction of disperse carbonitrides on such crystal lattice defects as dislocations.
机译:在853 K的温度下,在氨和丙烷-丁烷气态环境下,氮和碳扩散合金化作用下,初始塑性变形在5-70%范围内对铁基合金表面层的组织形成和力学性能的影响。研究了0.5-6小时。通过X射线衍射,显微硬度和耐磨性测试研究了表面扩散层。建立的氮和碳气体饱和后的铁合金表面层由六方密排晶体结构的ε相或与渗碳体晶格等构的正交晶结构的θ相组成。 α相在25-30%范围内的变形显着影响表面扩散层的结构,相和化学组成及性能。在90%氨和10%丙烷-丁烷的混合气体中,在25%至30%的变形和饱和后,层中出现θ-相。以这种方式获得的层显示出最大的显微硬度,耐磨性和厚度。变形后超出25-30%范围的合金中会形成ε相。含氮和碳的α相的晶格间距在塑性变形的25-40%范围内非线性减小。我们假设表面层的高度强化是由于碳氮化物在位错等晶格缺陷上的相互作用所致。

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