Albakry Mohammad, Guazzato Massimiliano, Swain Michael Vincent
Biomaterials Science Research Unit, Faculty of Dentistry, University of Sydney, United Dental Hospital, Surry Hills, NSW 2010, Australia.
J Prosthodont. 2004 Sep;13(3):141-9. doi: 10.1111/j.1532-849X.2004.04025.x.
This study evaluated the biaxial flexural strength and identified the crystalline phases and the microstructural features of pressed and repressed materials of the glass ceramics, Empress 1 and Empress 2.
Twenty pressed and 20 repressed disc specimens measuring 14 mm x 1 mm per material were prepared following the manufacturers' recommendations. Biaxial flexure (piston on 3-ball method) was used to assess strength. X-ray diffraction was performed to identify the crystalline phases, and a scanning electron microscope was used to disclose microstructural features.
Biaxial flexural strength, for the pressed and repressed specimens, respectively, were E1 [148 (SD 18) and 149 (SD 35)] and E2 [340 (SD 40), 325 (SD 60)] MPa. There was no significant difference in strength between the pressed and the repressed groups of either material, Empress 1 and Empress 2 (p > 0.05). Weibull modulus values results were E1: (8, 4.7) and E2: (9, 5.8) for the same groups, respectively. X-ray diffraction revealed that leucite was the main crystalline phase for Empress 1 groups, and lithium disilicate for Empress 2 groups. No further peaks were observed in the X-ray diffraction patterns of either material after repressing. Dispersed leucite crystals and cracks within the leucite crystals and glass matrix were features observed in Empress 1 for pressed and repressed samples. Similar microstructure features--dense lithium disilicate crystals within a glass matrix--were observed in Empress 2 pressed and repressed materials. However, the repressed material showed larger lithium disilicate crystals than the singly pressed material.
Second pressing had no significant effect on the biaxial flexural strength of Empress 1 or Empress 2; however, higher strength variations among the repressed samples of the materials may indicate less reliability of these materials after second pressing.
本研究评估了玻璃陶瓷Empress 1和Empress 2压制和再压制材料的双轴弯曲强度,并确定了其晶相和微观结构特征。
按照制造商的建议,为每种材料制备了20个压制和20个再压制的圆盘试样,尺寸为14 mm×1 mm。采用双轴弯曲(活塞对三球法)评估强度。进行X射线衍射以确定晶相,并使用扫描电子显微镜揭示微观结构特征。
压制和再压制试样的双轴弯曲强度分别为:Empress 1 [148(标准差18)和149(标准差35)]MPa以及Empress 2 [340(标准差40),325(标准差60)]MPa。Empress 1和Empress 2这两种材料的压制组和再压制组之间的强度无显著差异(p>0.05)。相同组的威布尔模量值结果分别为:Empress 1:(8,4.7)和Empress 2:(9,5.8)。X射线衍射显示,Empress 1组的主要晶相为白榴石,Empress 2组为二硅酸锂。再压制后,两种材料的X射线衍射图谱中均未观察到其他峰。在Empress 1的压制和再压制样品中观察到的特征是分散的白榴石晶体以及白榴石晶体和玻璃基质内的裂纹。在Empress 2的压制和再压制材料中观察到类似的微观结构特征——玻璃基质内致密的二硅酸锂晶体。然而,再压制材料中的二硅酸锂晶体比单次压制材料中的更大。
二次压制对Empress 1或Empress 2的双轴弯曲强度无显著影响;然而,材料再压制样品中较高的强度变化可能表明二次压制后这些材料的可靠性较低。