冷加工高熵合金Al0.3CoCrFeNi退火过程中的组织转变

I. Ivanov, K. Emurlaev, K. Kuper, D. Safarova, I. Bataev
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摘要

研究了高熵合金Al0.3CoCrFeNi在退火过程中的组织转变特征。对氩弧熔炼得到的钢锭进行压缩比为50%的冷轧。生产的工件在200、400、600、800和1000℃的温度下在炉中退火4小时。用同步加速器x射线衍射法和背散射电子衍射法对所制备的样品进行了检测。研究数据表明,在600℃以下,合金的组织为面心立方晶格的单相。当合金在800和1000℃下退火时,相组成的特征是存在两相:具有面心立方晶格的无序相和具有原始立方晶格的有序相。在温度高于800℃时,合金的燃烧伴随着再结晶过程的发展。结果表明,在800℃退火后,角间取向偏差大于10°的微体积相对比例为20%,在1000℃退火后为65%。在所研究的样品中,显微硬度随温度的升高而升高,最高可达600℃,随温度的进一步升高而降低。用衍射图剖面分析的方法分析衍射最大值的宽度表明,有序相的晶格畸变有所增加。这种行为可能与主相基体中纳米级夹杂物的释放有关。
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Structural transformations during annealing of cold-worked high-entropy alloy Al0.3CoCrFeNi
The paper considers the features of structural transformations during annealing of the high-entropy alloy Al0.3CoCrFeNi. The ingots obtained by argon arc melting were subjected to cold rolling with a compression ratio of 50 %. The produced worpieces were annealed in the furnace for 4 hours at temperatures of 200, 400, 600, 800 and 1000 °C. The samples obtained by the described technique were examined using the methods of synchrotron X-ray diffraction in the lumen mode and diffraction of backscattered electrons. The research data indicate that up to a temperature of 600 °C, the structure of the alloys is represented by a single phase with a face-centered cubic lattice. When annealing alloys at temperatures of 800 and 1000 °C, the phase composition is characterized by the presence of two phases: a disordered phase with a face-centered cubic lattice and an ordered phase with a primitive cubic lattice. At temperatures above 800 °C, the burning of alloys is accompanied by development of recrystallization processes. It was found that after annealing at 800 °C, the relative proportion of micro-volumes characterized by inter-angular misorientation of more than 10° was 20 %, and after annealing at 1000 °C – 65 %. Microhardness of the studied samples increases with an increase in temperature up to 600 °C and decreases with a further increase in temperature. Analysis of the width of diffraction maxima using the methods of profile analysis of diffractograms indicates an increase in distortions of the crystal lattice of the ordered phase. This behavior may be associated with the release of nanoscale inclusions in the matrix of the main phase.
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