Effects of Y2O3 Doping on Sintering Properties and Microstructure of CaTiO3 Ceramics
摘 要
以CaO和TiO2为原料,外加质量分数分别为0,1%,2%,3%,4%的Y2O3后,分别在1 300,1 400℃保温3 h烧结制备CaTiO3陶瓷,研究Y2O3掺杂量和烧结温度对陶瓷物相组成、晶体结构、烧结性能和微观结构的影响。结果表明:随着Y2O3掺杂量的增加,CaTiO3的晶胞体积先增大后减小,Y3+置换Ti4+使CaTiO3晶胞体积增大,置换Ca2+则使晶胞体积减小;随Y2O3掺杂量的增加或烧结温度的升高,陶瓷的烧结线收缩率和体积密度均增大;随Y2O3掺杂量的增大,陶瓷的显微结构更为致密,CaTiO3晶粒尺寸先增大后减小,晶粒形状由不规则台阶状转变为规则形状。
Abstract
CaTiO3 ceramics were prepared at 1 300,1 400℃ for 3 h with CaO and TiO2 as raw materials and being doped with 0, 1wt%, 2wt%, 3wt%, and 4wt% Y2O3. The effects of Y2O3 doping amount and sintering temperature on the phase composition, crystal structure, sintering properties and microstructure of the ceramics were investigated. The results show that the cell volume of CaTiO3 first increased and then decreased with increasing Y2O3 doping amount. The substitution of Y3+ for Ti4+ increased the cell volume of CaTiO3 while the substitution of Y3+ for Ca2+ reduced the cell volume. With the increase of Y2O3 doping amount or the rise of sintering temperature, both the sintering linear shrinkage rate and the bulk density of the ceramics increased. With the increase of Y2O3 doping amount, the microstructure of the ceramics became denser, the size of CaTiO3 grains first increased and then decreased, and the grain shape changed from step-like morphology to regular polygons.
中图分类号 TQ174 DOI 10.11973/jxgccl201804012
所属栏目 材料性能及应用
基金项目 国家自然科学基金资助项目(51402143);辽宁省自然科学基金资助项目(601009802)
收稿日期 2017/7/26
修改稿日期 2018/2/25
网络出版日期
作者单位点击查看
备注安迪(1992-),男,河南商丘人,硕士研究生
引用该论文: AN Di,LUO Xudong,LIU Pengcheng,XIE Zhipeng,LI Ting. Effects of Y2O3 Doping on Sintering Properties and Microstructure of CaTiO3 Ceramics[J]. Materials for mechancial engineering, 2018, 42(4): 53~57
安迪,罗旭东,刘鹏程,谢志鹏,李婷. Y2O3掺杂对CaTiO3陶瓷烧结性能和微观结构的影响[J]. 机械工程材料, 2018, 42(4): 53~57
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【3】MANIK S K, PRADHAN S K. Microstructure characterization of ball milled prepared monocrystalline perovskite CaTiO3 by Rietveld method[J]. Materials Chemistry & Physics, 2004, 86(2/3):284-292.
【4】陈万兵, 张少伟, 王周福,等. 熔盐合成法制备CaTiO3粉体的研究[J]. 武汉科技大学学报, 2007, 30(6):581-583.
【5】彭子飞, 汪国忠, 张伟,等. 化学共沉淀法制备纳米级CaTiO3粉体[J]. 功能材料, 1996, 27(5):429-430.
【6】张启龙, 王焕平, 杨辉. CaTiO3纳米粉体溶胶-凝胶法合成、表征及介电特性[J]. 无机化学学报, 2006, 22(9):1657-1662.
【7】关志刚, 罗旭东, 王强. Er2O3对CaTiO3/CaAl12O19材料结晶性能的影响[J]. 材料热处理学报, 2014, 35(7):53-58.
【8】DERE AN'G P J, MAHIOU R, PAZIK R, et al. Upconversion emission in CaTiO3:Er3+ nanocrystals[J]. Journal of Luminescence, 2008, 128(5/6):797-799.
【9】MAR AI'G B, SINGH K C, CEMBRERO-COCA P, et al. Red emitting MTiO3 (M=Ca or Sr) phosphors doped with Eu3+ or Pr3+ with some cations as co-dopants[J]. Displays, 2013, 34(4):346-351.
【10】BASSOLI M, BUSCAGLIA M T, BOTTINO C, et al. Defect chemistry and dielectric properties of Yb3+:CaTiO3 perovskite[J]. Journal of Applied Physics, 2008, 103(1):014104.
【11】TALANTIKITE D, TAÏBI-BENZIADA L. Phase transitions of CaTiO3 ceramics sintered with the aid of NaF and MgF2[J]. Solid State Sciences, 2009, 11(1):151-155.
【12】SEBASTIAN M T, SANTHA N, BIJUMON P V, et al. Microwave dielectric properties of (1-x)CeO2-xCaTiO3, and (1-x)CeO2-xSm2O3 ceramics[J]. Journal of the European Ceramic Society, 2004, 24(9):2583-2589.
【13】BUSCAGLIA M T, VIVIANI M, BUSCAGLIA V, et al. Incorporation of Er3+ into BaTiO3[J]. Journal of the American Ceramic Society, 2002, 85(6):1569-1575.
【14】齐建全, 李龙土, 王永力. 钛酸钡陶瓷中Y2O3掺杂过程的XRD分析[J]. 稀有金属材料与工程, 2002, 31(1):237-240.
【15】雷文, 吕文中, 王晓川,等. CaTiO3对(1-x)ZnAl2O4-xMg2TiO4(x=0.21)微波介质陶瓷结构和性能的影响[J]. 无机材料学报, 2009, 24(5):957-961.
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