欢迎登录材料期刊网

材料期刊网

高级检索

采用XRD技术研究了固相反应制备Sm2Zr2O7的形成机制.结果表明:从1000℃开始,Sm3+逐渐取代Zr4+的位置,形成萤石结构ZrO2-Sm2O3固溶体,该过程直到1400 ℃才基本结束:在1200 ℃~1300 ℃之间,Sm2O3与ZrO2发生固溶的同时,固溶体开始转变为焦绿石结构的Sm2Zr2O7,到1500 ℃所有固溶体完全转变为Sm2Zr2O7:1500 ℃以后,Sm2Zr2O7晶体逐渐长大并最终形成理想的Sm2Zr2O7晶体.整个过程并无其它中间相生成.

参考文献

[1] Nitin P;Gell M;Jordan Eh .[J].Science,2002,296:280.
[2] Beele W;Marijnissen G;Van A et al.[J].Surface and Coatings Technology,1999,120:61.
[3] Cao X Q;Vasseh R;Stoever D .[J].Journal of the European Ceramic Society,2000,24:1.
[4] Bast U;Schumann E .[J].Ceramic Engineering and Science Proceedings,2002,23:525.
[5] Garlos G Levi .[J].Current Opinons in Solid State and Materials Science,2004,8:77.
[6] Girijia Suresh;Seenivasan G;Krishnaiah M V et al.[J].Journal of Nuclear Materials,1997,49:259.
[7] Xu Qiang;Pan Wei;Wang Jingdong et al.[J].Materials Letters,2005,59:2804.
[8] Saruhan B;Francois P;Fritscher K;Schulz U .EB-PVD processing of pyrochlore-structured La2Zr2O7-based TBCs[J].Surface & Coatings Technology,2004(2/3):175-183.
[9] Fuertes M C;Salgueiro W;Somoza A et al.[J].Scripta Materialia,2004,50:301.
[10] Fuertes M C;Porto Lopez J M .[J].Ceramics International,2004,30(08):2137.
[11] Yshima M;Ishizwa N;Yoshimura M .[J].Journal of the American Ceramic Society,1992,75:1541.
[12] Yshima M;Ishizwa N;Yoshimura M .[J].Journal of the American Ceramic Society,1992,75:1550.
[13] Michel D;Faudot F;Gaffet E et al.[J].Journal of the American Ceramic Society,1993,76:2884.
[14] Glzazchev V S;Lukin E S;Balashev V A et al.[J].Inorganic Materials,1977,13(10):1461.
[15] Chistyi I L;Fabelinskii I L;Kitaeva V F et al.[J].Journal of Raman Spectropy,1977,6(04):183.
[16] Levitski V A;Narchuk P B;Hekimov et al.[J].Journal of Solid State Chemistry,1977,20(02):119.
[17] 苏锵.稀土化学[M].郑州:河南科学技术出版社,1993:203.
[18] 樊先平;洪樟连;翁闻剑.无机和纳米材料理论基础[M].杭州:浙江大学出版社,2003:210.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%