首页> 外文会议>International Conference on New Frontiers of Processing and Engineering in Advanced Materials >Challenges in Joining Advanced Ceramic Materials: Interface Formation of Ceramic/Metal High-Temperature Brazes
【24h】

Challenges in Joining Advanced Ceramic Materials: Interface Formation of Ceramic/Metal High-Temperature Brazes

机译:加入先进陶瓷材料的挑战:陶瓷/金属高温钎料的界面形成

获取原文

摘要

This paper describes the metallurgical interfacial reactions at elevated temperatures between reactive zirconium metal and stable oxide ceramics, specifically beryllia, yttria, and magnesia- zirconia composite ceramic. The ceramic/metal systems were preheated at 600°C, and then heated to peak temperatures of 1800°C or above, depending of the system, in ultra pure Argon atmosphere. After a short stay at the peak temperature, each system was cooled to room. The interaction was monitored during heating by a video camera and the interfaces were microscopically examined after the thermal cycle. The microstructure and chemical changes at the interface were evaluated via SEM and EDS. During heating of the beryllia/Zr system, the ceramic was initially reduced and Be alloyed the Zr metal in solid solution, causing Zr to melt locally at the interface at about 1600°C instead of 1855°C. The alloy Zr-Be liquid is what later dissolved the beryllia and infiltrated partially into the ceramic substrate. It seems that there was no solid state reaction between the Zr metal and yttria since Zr melted at its melting temperature of 1855°C; it is evident, however, that the liquid Zr partially dissolved yttria at the interface; yttrium and oxygen segregated to the grain boundaries. The solidified metal tightly bonded to the ceramic substrate as the system cooled to room temperature. In the Zr-MgO/ZrO_2 system, Zr melted at 1855°C and it reduced the magnesia, but at the same time the magnesium was volatilized.
机译:本文介绍了反应性锆金属和稳定氧化物陶瓷,特别是铍,氧化钇和氧化锆复合陶瓷之间的升高温度下的冶金界面反应。将陶瓷/金属系统在600℃下预热,然后在超纯氩气氛中加热至1800℃或更高的峰值温度,或以上的峰值温度。在峰值温度下保持短暂停留后,将每个系统冷却至室内。在通过摄像机加热期间监测相互作用,并且在热循环之后进行接口进行显微镜。界面的微观结构和化学变化通过SEM和EDS评估。在加热铍/ Zr系统期间,最初还原陶瓷,并将Zr金属合金化在固溶体中,使Zr在约1600℃而不是1855℃的界面处局部熔化。合金Zr-Be液体后来溶解了铍并部分地渗透到陶瓷基材中。似乎在Zr金属和ytTria之间没有固态反应,因为Zr在1855°C的熔化温度下熔化;然而,很明显,液体Zr部分溶解在界面处的YtTria;钇和氧气分离到晶界。当系统冷却至室温时,将固化金属紧密结合到陶瓷基板上。在Zr-MgO / ZrO_2系统中,Zr在1855℃熔化并降低氧化镁,但同时镁挥发。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号