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以ZrO2质定径水口基质为研究对象,在脱硅锆细粉中添加稳定剂,其中稳定剂的种类和加入量分别为2.8%MgO、2.1%MgO、2.2%MgO+1%Y2 O3.借助XRD、SEM和EDS等检测手段,研究了稳定剂对ZrO2质定径水口基质烧成前后相组成和显微结构的影响.结果表明,试样经1630℃烧成,各试样立方相含量明显增加,单斜相含量明显减少,原料中稳定剂的种类和加入量的不同使得烧成后各试样立方相和单斜相的变化量也不相同;试样经1630℃烧成,稳定剂MgO 与ZrO2形成固溶体,越靠近 MgO 颗粒的位置Mg2+与Zr4+的替换程度越明显,但稳定剂的扩散固溶远未达到均匀状态;以MgO+Y2 O3为稳定剂的试样,烧成后立方相的增加量最多,固溶体的生成量最大,稳定化程度最高,且 ZrO2颗粒的尺寸大小均匀,棱角分明,颗粒之间的结合非常紧密.

ZrO2 sizing nozzle matrix was researched by adding stabilizer which were 2.8%MgO,2.1%MgO and 2.2%MgO+1%Y2 O3 respectively in the desilication zirconium powder.The effects of stabilizer on the composi-tion of phase and the microstructure of ZrO2 sizing nozzle matrix before and after sintering were studied by XRD,SEM and EDS.Results showed that the content of cubic phase increased and the content of monoclinic phase decreased significantly for all samples after sintering at 1 630 ℃,the specise and feed ratio of stabilizer in raw materials made cubic and monoclinic phase variation of each sample were not the same after sintering;After sintering at 1 630 ℃,the solid solution was formed by MgO and ZrO2 ,with the location of MgO particle clos-er,the substitution degree of Mg2+ and Zr4+ was more obvious,but the diffusion and solid solution of the stabi-lizer were far from uniform state;For the sinteried sample combining MgO+Y2 O3 stabilizer,cubic phase gained the most,and solid solution generated largest,the degree of stabilization was the highest and the combi-nation between ZrO2 particles which have uniform size and angular shape is much close.

参考文献

[1] 贺中央.连铸用功能耐火材料的现状及发展趋势[J].耐火材料,2011(06):462-465,474.
[2] Trueba Jr;Luis;Peasiee Kent D;Smith Jeffrey D et al.Effect of nozzle base material on the rate of clogging dur-ing the continuous casting of aluminum-killed steels[J].Steel Research International,2006,77(1):37-47.
[3] Tian Xiaoli;Xue Qunhu;Xue Chongbo .Study on proper-ties of alunina-zirconia sizing nozzle[J].Bulletin of the Chinese Ceramic Society,2010,29(4):918-921.
[4] Duh Jenggong;Dai Hsingtao .Sintering,microstrcuture,hardness and fracture toughness behavior of Y2 O3-CeO2-ZrO2[J].Journal of the American Ceramic Society,1988,71(10):813-819.
[5] 余鑫萌,徐宝奎,袁发得.二氧化锆的稳定化及其应用[J].稀有金属快报,2007(01):28-32.
[6] Yin Yansheng;Li Jia.Zirconia ceramics and its composites materials[M].北京:化学工业出版社,2004:1-9.
[7] 林振汉,林钢,吴亮,张玲秀.氧化锆系的相结构和转变[J].稀有金属,2003(01):49-52.
[8] Jerome Chevalier;Laurent Gremillard;Anil V. Virkar .The Tetragonal-Monoclinic Transformation in Zirconia: Lessons Learned and Future Trends[J].Journal of the American Ceramic Society,2009(9):1901-1920.
[9] Tan Qinghua;Geng Keming;Wu Aijun.Effect of stabilizer on phase composition,microstructure and prop-erties of zirconia products[A].,2009:1528-1533.
[10] Emad Mustafa;Matthias Wilhelm;Werner Wruss .Phasestability and microstructural characteristics of 12mol%(Mg,Ca)-PSZ prepared via polymeric route[J].Ceram-ics International,2003,29(2):189-194.
[11] Yannick Hemberger;Christoph Berthold;Klaus G. Nickel .Wetting and corrosion of yttria stabilized zirconia by molten slags[J].Journal of the European Ceramic Society,2012(11):2859-2866.
[12] 杜娟,李伟,金学军,蒋丹宇,施剑林.四方相纳米氧化锆低温稳定机制的研究现状[J].功能材料,2006(11):1691-1696.
[13] 陈岚,李锐星,梁焕珍,喻克宁,白辰东.ZrO2陶瓷的制备及应用研究进展[J].功能材料,2002(02):129-132,135.
[14] Yuan Zhangfu;Wan Tianji;Zhang Jian et al.Production of ZrO2 by plasma and its application on tundish[J].Journal of University of Science and Technology Beijing,1993,15(5):479-484.
[15] Okada H;Tamura T;Ramakrishnan N et al.Analysis of toughening of magnesia partially stabilized zirconia,due to dilatation transformation[J].Acta Metallurgic et Ma-terialia,1992,40(6):1421-1432.
[16] Hannink R.H.J.;Kelly P.M. .Transformation Toughening in Zirconia-Containing Ceramics[J].Journal of the American Ceramic Society,2000(3):461-487.
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