定向凝固DZ444镍基高温合金初生MC碳化物的分解行为
肖旋, 女, 1966年生, 副教授, 博士
修回日期: 2013-12-25
网络出版日期: 2014-09-25
基金资助
*国家自然科学基金资助项目 51001101
THE DECOMPOSITION BEHAVIOR OF PRIMARY MC CARBIDE IN NICKEL BASE DIRECTIONALLY SOLIDIFIED SUPERALLOY DZ444
Revised date: 2013-12-25
Online published: 2014-09-25
Supported by
Supported by National Natural Science Foundation of China (No.51001101)
研究了定向凝固镍基高温合金DZ444在800, 850和900 ℃下最长达104 h长期时效过程中初生MC碳化物的热稳定性、MC分解机制及其分解对组织演化的影响. 结果表明: DZ444合金初生MC碳化物的热稳定性较低. 在长期时效过程中, MC分解不断加剧; 同时, MC分解区域内产物不断发生变化, 在MC分解初期产生了典型的SM结构(sandwich microstructure), 在MC分解中期出现了h相, 在MC分解末期析出一定量的h-M6C和h-M23C6. MC分解过程可以大体地描述为: MC+g→SM-M23C6+SM-M6C+SM-g'→SM-M23C6+SM-M6C+SM-g'+h→SM-M23C6+SM-M6C+SM-g'+h+h-M6C+h-M23C6, 其中二次碳化物的类型主要为M23C6, 且随着时效温度的升高和时效时间的延长, 二次M6C含量略有增加. MC的分解能够促进晶内M23C6沉淀、s相析出和晶界粗化.
肖旋 , 曾超 , 侯介山 , 秦学智 , 郭建亭 , 周兰章 . 定向凝固DZ444镍基高温合金初生MC碳化物的分解行为[J]. 金属学报, 2014 , 50(9) : 1031 -1038 . DOI: 10.11900/0412.1961.2013.00836
Hot-corrosion directionally solidified Nickel base superalloy DZ444 is generally used as the candidate material for blade of gas turbine, which required excellent alloy microstructural stability. As one of the constitutional phase of the alloy, primary MC carbides are often thermally unstable, and its degradation reactions can happen when the alloys are in services or thermally exposed in high temperature circumstances. There existed several different kinds of MC decompostion reactions in some traditional Ni-based superalloys. To figure out the thermal stability of primary MC carbide in the DZ444 alloy and better understand its degradation mechanism, some related discussions to the thermal stability and degeneration process of primary MC carbide and its effects on the microstructure were made. In this work, microstructures of DZ444 alloy after long-term exposure up to 1×104 h at 800, 850 and 900 ℃ have been observed by OM, SEM and TEM. The results show that the thermal stability of MC was low. As long-term exposure proceeds, MC decompostion became more and more serious. Firstly, a typical sandwich microstructure (SM) gradually formed and thickened in the MC/g interface; secondly, h phase precipitated in the SM/MC interface; lastly, h-M6C and h-M23C6 locally precipitated inside the h phase. Finally, SM structure, h phase, h-M6C and h-M23C6 successively formed in MC degeneration areas at three stages of its decomposition process. Basically, MC decompostion process could be described with such raction formula as follows: MC+g→SM-M23C6+SM-M6C+SM-g'→SM-M23C6+SM-M6C+SM-g'+h→SM-M23C6+SM-M6C+SM-g'+h+h-M6C+h-M23C6. Generally, the type of secondary carbide from MC degeneration was M23C6, and, with the increase of long-term exposure temperature and time, the amount of secondary M6C carbide slightly increased. Besides, MC degeneration might result in the precipitation of transgranular M23C6 carbide and s phase in the vicinity of MC degeneration areas, and the coarsening of grain boundary (GB).
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