首页 | 本学科首页   官方微博 | 高级检索  
     

Thermodynamic analysis of Ti powder synthesized by SHS thermitreaction
作者姓名:张鹏林  夏天东  张国栋  闫丽静  赵文军
作者单位:[1]State Key Laboratory of Gansu Advanced Nonferrous Metal Materials, Lanzhou University of Technology, Lanzhou 730050, China [2]Key Laboratory of Non-ferrous Metal Alloys, Ministry of Education, Lanzhou University of Technology, Lanzhou 730050, China [3]College of Power and Mechanical Engineering, Wuhan University, Wuhan 430072, China
摘    要:

关 键 词:高温合成技术  热力学分析  隔热技术      合金
收稿时间:2007-07-15
修稿时间:2007-09-10

Thermodynamic analysis of Ti powder synthesized by SHS thermitreaction
ZHANG Peng-lin, XIA Tian-dong, ZHANG Guo-dong, YAN Li-jing, ZHA Wen-jun.Thermodynamic analysis of Ti powder synthesized by SHS thermitreaction[J].Transactions of Nonferrous Metals Society of China,2007,17(A01):27-31.
Authors:ZHANG Peng-lin  XIA Tian-dong  ZHANG Guo-dong  YAN Li-jing  ZHA Wen-jun
Affiliation:ZHANG Peng-lin, XIA Tian-dong, ZHANG Guo-dong, YAN Li-jing, ZHA0 Wen-jun
Abstract:According to the thermodynamics theories, the reactive Gibbs free energies, the reactive adiabatic temperature, the melting rate of Ti and the gasification mass of Mg in the Mg-TiO2 and AI-TiO2 systems were theoretically calculated and analyzed respectively. The results show that the reactions of Mg-TiO2 and AI-TiO2 are very easy to take place and the reaction of producing various suboxides of Ti may occur in Mg-TiO2 and AI-TiO2 reaction system; the adiabatic temperature of Mg-TiO2 becomes lower with increasing mass fraction of Mg. The adiabatic temperature is below 1 800 K when the mass fraction of excessive Mg exceeds 25%; The adiabatic temperature of AI-TiO2 also becomes lower with increasing mass fraction of AI, but it becomes higher with the preheat temperature increment. The adiabatic temperature plateau is the result of Ti melting endotherm; owing to the gasification of a great deal of Mg in Mg-TiO2 reaction process, Mg should be properly excessive in order to get Ti.
Keywords:
本文献已被 维普 等数据库收录!
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