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Segregation Effects and Phase Developments during Solidification of Alloy 625

机译:合金625凝固过程中的分离效应和相位发展

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The solidification behaviour of pure Alloy 625, and Alloy 625 enriched respectively in iron and carbon, was investigated in situ by hot-stage light optical microscopy. Using this technique planar front solidification for distances of several hundred microns was facilitated. After solidification, the material that experienced planar front solidification corresponded accurately to that of dendrites tens of microns in width adopting an equivalent dendrite arm width approach. Eventually, the planar solidification front broke down, where after the residual liquid solidified eutectic-like. This material contained y-phase, Laves phase and, if carbon was dissolved in the liquid, niobium rich carbides formed. Molybdenum and niobium showed strong tendencies to segregate. Their segregation was balanced by inverse segregation of nickel and iron. The chromium concentration remained almost constant in y in the entire matrix material. Addition of carbon did not cause detectable alterations of the material that experienced planar front solidification. However, it promoted the formation of niobium rich carbides in the material that solidified eutectic-like. Thus, this material differed from that of the pure sample in constitution, and consequently in y-phase composition. Niobium rich carbides formed prior to Laves phase; in carbon rich volumes only the carbides form. As compared to the pure sample, the sample enriched in iron had decreased global minimal solute concentration in the material that experienced planar front solidification. However, once the concentrations were corrected with respect to the dilution simply caused by the presence of iron, the solidification behaviour in this material was identical to that of the pure sample. The constitution in the material that solidified eutectic-like was y and Laves phase. As compared to the pure sample, the Laves phase was enriched in iron.
机译:通过热级光学显微镜研究纯合金625和富含铁和碳中富含铁和碳的合金625的凝固行为。使用该技术,促进了几百微米距离的平面凝固。在凝固之后,经历平面前凝固的材料可准确地对应于树枝状的宽度,其宽度的垂直是相当于等效的树突臂宽度方法。最终,平面凝固前部突破,其中残留液体固化后的共晶样。该材料含有Y相,疏浚阶段,如果碳溶于液体中,则形成富含碳化铌的碳化铌。钼和铌表现出强烈的隔离倾向。他们的隔离是通过镍和铁的逆分离来平衡的。在整个基质材料中,铬浓度在Y中几乎恒定。添加碳并未引起经历平面前固化的材料的可检测改变。然而,它促进了富含共晶样的材料中富含富含碳化铌的铌。因此,这种材料与构造中的纯样品的材料不同,因此在Y相组合物中不同。富含铌的碳化物在疏浚阶段形成;在碳含量富含碳化物形式。与纯样品相比,富含铁的样品在经历平面前固化的材料中降低了全球性最小溶质浓度。然而,一旦浓度相对于稀释浓度校正,即仅由铁的存在引起的,该材料中的凝固行为与纯样品的凝固行为相同。固化共晶样的材料中的构造是y和疏浚阶段。与纯样品相比,熔化液相富含铁。

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