加入高含量铪或钽的含碳等摩尔CoNiFeMnCr合金在1000℃下的氧化行为

P. Berthod
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引用次数: 0

摘要

在这项工作中,hfc和tac增强的铸型等摩尔CoNiFeMnCr合金(Cantor)在实验室空气中1000°C氧化测试。铬似乎和锰一样,都是选择性氧化元素。外部形成的主要氧化物是M2O3氧化物,其中Mn和Cr以不同比例存在,这取决于与合金表面的接近程度。靠近氧化锋的HfC碳化物在HfO2中原位氧化,随后碳的释放向内扩散,并诱导块状或针状碳化物的固态析出。靠近氧化锋的TaC碳化物由于溶解而表现出不同的行为,Ta向氧化锋扩散形成CrTaO4氧化物。即使在1000℃下加热50 h,亚表面也或多或少地出现了Cr和Mn的深度贫化,其中Mn含量极低。Cr和Mn含量的评价以及等效氧化厚度和动力学氧化常数的开发结果表明,合金的抗氧化性很弱,必须显著提高,以便在实际应用中受益于此类合金优越的高温机械抗力。为此,提出了一些方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Behavior in Oxidation at 1000°C of Carbon-Containing Equimolar CoNiFeMnCr Alloys Added with Hafnium or Tantalum with High Contents
In this work, HfC–and TaC–reinforced cast versions of the equimolar CoNiFeMnCr alloy (Cantor) were tested in oxidation at 1000°C in laboratory air. Chromium seemingly shared, with manganese, its role as a selectively oxidized element. The principal oxide to form externally was an M2O3 one in which Mn and Cr were present in various proportions depending on the proximity with the alloy’s surface. The HfC carbides close to the oxidation front were oxidized in situ in HfO2, with the release of carbon diffusing inwards after that and inducing the solid-state precipitation of blocky or acicular chromium carbides. The behavior of the TaC carbides present close to the oxidation front was different since they dissolved, and Ta diffused towards the oxidation front to form CrTaO4 oxides. Even after 50 hours at 1000°C, the subsurfaces were more or less deeply impoverished in Cr and Mn, with minimal contents meager, especially for Mn. The evaluation of the Cr and Mn quantities and the exploitation of results in terms of equivalent oxide thickness and kinetic oxidation constant demonstrates that the resistance of the alloys against oxidation is feeble and must be significantly improved to allow benefiting of the superior high-temperature mechanical resistances of such alloys in practical application. For that, some ways are proposed.
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