首页 | 本学科首页   官方微博 | 高级检索  
     

金属热还原法制备钛铝中间合金
引用本文:宋玉来.,豆志河.,张廷安,刘燕,牛丽萍.金属热还原法制备钛铝中间合金[J].稀有金属材料与工程,2020,49(3):1015-1019.
作者姓名:宋玉来.  豆志河.  张廷安  刘燕  牛丽萍
作者单位:多金属共生矿生态化冶金教育部重点实验室,冶金学院 东北大学 沈阳;多金属共生矿生态化冶金教育部重点实验室,冶金学院 东北大学 沈阳;多金属共生矿生态化冶金教育部重点实验室,冶金学院 东北大学 沈阳;多金属共生矿生态化冶金教育部重点实验室,冶金学院 东北大学 沈阳;多金属共生矿生态化冶金教育部重点实验室
基金项目:重点基础研发计划(项目编号2017YFB0305401-2);中央直属高校基本业务费(项目编号: N170908001、 N172506009)
摘    要:以TiO_2为原料,KClO_3为发热剂,Al为还原剂和合金化剂,Ca为深度还原剂,通过金属热还原法制备钛铝中间合金,考察了单位质量热效应、造渣剂配比和还原剂加入量及组成对反应过程稳定性、合金成分及收率的关系。研究表明:用Ca和Al作为还原剂时,体系绝热温度分别是2426和1806 K,反应制得的钛铝中间合金由Ti Al、Ti_3Al和少量的Al_2O_3夹杂相组成,化学分析合金中Ti、Al、O质量分数分别为58.36%、40.19%和1.41%。

关 键 词:钛铝中间合金  单位质量热效应  绝热温度  金属热还原
收稿时间:2019/1/17 0:00:00
修稿时间:2019/7/12 0:00:00

Preparation of TiAl Alloy by Metallothermic Reduction
Song Yulai.,Dou Zhihe.,Zhang Ting-an,Liu Yan and Niu Liping.Preparation of TiAl Alloy by Metallothermic Reduction[J].Rare Metal Materials and Engineering,2020,49(3):1015-1019.
Authors:Song Yulai  Dou Zhihe  Zhang Ting-an  Liu Yan and Niu Liping
Abstract:The low cost preparation of TiAl master alloy is an important direction of current research. In this paper, TiO2 as raw material, KClO3 as heating agent, Al as reducing agent and alloying agent, Ca as deep reducing agent were used for the preparation of TiAl master alloy by metallothermic reduction method. The heat effect per unit mass, the proportion of slag-making agent, the amount and composition of reducing agent on the stability of the reaction process, the composition and yield of alloy were investigated. The results showed that when Ca and Al were used as reducing agents, the adiabatic temperature of the system was 2426 K and 1806 K, respectively. The TiAl master alloy was composed of TiAl, Ti3Al and a small amount of Al2O3 inclusions. The contents of Ti, Al and O in the alloy were 58.36%, 40.19% and 1.41%, respectively.
Keywords:TiAl intermetallic alloy  heat effect per unit mass  adiabatic temperature  metallothermic reduction
本文献已被 CNKI 等数据库收录!
点击此处可从《稀有金属材料与工程》浏览原始摘要信息
点击此处可从《稀有金属材料与工程》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号