Heat treatment induced phase transformations in zirconia and yttria-stabilized zirconia monolithic aerogels

被引:30
作者
Torres-Rodriguez, Jorge [1 ]
Kalmar, Jozsef [2 ,3 ]
Menelaou, Melita [1 ]
Celko, Ladislav [1 ]
Dvorak, Karel [4 ]
Cihlar, Jaroslav [1 ]
Cihlar, Jaroslav, Jr. [1 ]
Kaiser, Jozef [1 ]
Gyori, Eniko [2 ]
Veres, Peter [2 ]
Fabian, Istvan [2 ,3 ]
Lazar, Istvan [2 ]
机构
[1] Brno Univ Technol, Cent European Inst Technol, Purkynova 123, Brno 61200, Czech Republic
[2] Univ Debrecen, Dept Inorgan & Analyt Chem, Egyetem Ter 1, H-4032 Debrecen, Hungary
[3] MTA DE Redox & Homogeneous Catalyt React Mech Res, Egyetem Ter 1, H-4032 Debrecen, Hungary
[4] Brno Univ Technol, Fac Civil Engn, AdMaS Ctr, Purkynova 139, Brno 61200, Czech Republic
关键词
Aerogel; Zirconia; Yttria-stabilized zirconia; Heat treatment; Phase transformation; SOL-GEL; TETRAGONAL ZIRCONIA; MESOPOROUS SILICA; STRATEGIES;
D O I
10.1016/j.supflu.2019.02.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Monolithic, structurally stable zirconia (ZrO2) aerogels can be used in high temperature applications and as medical implants. The macroscopic properties of these solids can be fine-tuned by the appropriate thermal treatment of the amorphous aerogels. Herein, we investigate the thermally induced phase transitions of ZrO2 and yttria-stabilized zirconia (YSZ) monolithic aerogels. All aerogels were produced by an acid-catalyzed sol-gel technique and subsequent supercritical drying (SCD). A complete reaction mechanism is proposed for the formation of the wet gel network. Also, the phase transformations taking place during calcination were followed as function of temperature by in-situ X-ray diffraction measurements. Composition and size of the forming crystallites were calculated from the XRD data. Phase transition is controlled by the temperature-dependent growth of crystallite size during calcination up to 1200 degrees C. Both tetragonal and monoclinic zirconia form in pure ZrO2 aerogels, and a single tetragonal phase forms in YSZ aerogels.
引用
收藏
页码:54 / 63
页数:10
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