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Examination of some high-strength, high-conductivity copper alloys for high-temperature applications

机译:检验高温应用中的某些高强度,高导电性铜合金

摘要

Copper alloys with high strength and high thermal and electrical conductivity have received a lot of attention over the last decades. Most of such efforts have concentrated on the development of alloys containing fine, dispersed particles, and using rapid solidification techniques to ensure a sufficient volume fraction and sufficient fineness of the dispersed phase. In a recent study, a Cu-8Cr-4Nb alloy was developed which shows relatively good strength up to 700 C, a result which was explained by the resistance to coarsening of the fine Cr{sub 2}Nb intermetallic particles in this materials. The amount of intermetallic Cr{sub 2}Nb second phase in this alloy was about 14vol% and it was claimed that the special compound-nature of the intermetallic phase was responsible for the good stability and retention of strength to high temperature. In order to examine the influence of the nature of the fine particles present and their stability against coarsening, as well as to examine the influence of volume fraction of second phase on tensile strength, three different alloys have been chosen for study: Cu-2Nb and Cu-4Cr for examining the role of second phase chemistry (Nb or Cr) on structural and property stability; and a Cu-14Cr alloy, for comparison with the Cu-4Cr alloy, to examine the role of volume fraction of the second phase. The stability of these alloys will then be compared with that reported for the Cu-8Cr-4Nb alloy.
机译:在过去的几十年中,具有高强度,高导热性和导电性的铜合金受到了很多关注。大多数这样的努力集中在开发包含细的,分散的颗粒的合金上,并使用快速固化技术来确保足够的体积分数和足够的分散相细度。在最近的一项研究中,开发了一种Cu-8Cr-4Nb合金,该合金在700℃以下显示出相对较好的强度,这一结果可以用这种材料中的Cr {sub 2} Nb细金属间化合物微粒的耐粗化性来解释。该合金中的金属间Cr {sub 2} Nb第二相的含量约为14vol%,并且据称金属间相的特殊化合物性质负责保持良好的稳定性并保持高温强度。为了检查存在的细颗粒的性质及其对粗化的稳定性的影响,以及检查第二相的体积分数对拉伸强度的影响,选择了三种不同的合金进行研究:Cu-2Nb和Cu-4Cr,用于检验第二相化学(Nb或Cr)对结构和性能稳定性的作用;为了与第二相Cu-4Cr合金进行比较,研究了第二相体积分数的作用。然后将这些合金的稳定性与报告的Cu-8Cr-4Nb合金的稳定性进行比较。

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  • 作者

    Dadras M.; Morris David G.;

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  • 年度 2013
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  • 原文格式 PDF
  • 正文语种 eng
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