Microstructural and mechanical analysis of two CAD-CAM lithium disilicate glass-reinforced ceramics

材料科学 抗弯强度 陶瓷 复合材料 粘结强度 二硅酸锂 扫描电子显微镜 微观结构 玻璃陶瓷 胶粘剂 多孔性 氢氟酸 冶金 图层(电子)
作者
Lucas do Nascimento Tavares,Karla Zancopé,Anielle Christine Almeida Silva,Luís Henrique Araújo Raposo,Carlos José Soares,Flávio Domingues das Neves
出处
期刊:Brazilian Oral Research [Brazilian Society of Dental Research]
卷期号:34: e004-e004 被引量:20
标识
DOI:10.1590/1807-3107bor-2020.vol34.0004
摘要

The aim of this study was to analyze the structural, morphological and mechanical properties of two different lithium disilicate glass-reinforced ceramics for CAD-CAM systems (IPS e.max CAD and Rosetta SM). Five methodologies were used for both ceramics: microstructure (n = 2) was analyzed using x-ray diffraction (XRD); morphological properties (n = 2) were analyzed by scanning electron microscopy (SEM), with and without hydrofluoric etching; porosity (n = 3) was assessed using 3D micro-computed tomography (micro-CT); flexural strength was measured (n =1 0) using the three-point bending test; and bond strength was determined with self-adhesive resin cement (n = 10), using a microshear bond test. After performing all the tests, the data were analyzed using t-Student test and two-way ANOVA. All the tests used a significance level of α = 0.05. High peak positions corresponding to standard lithium metasilicate and lithium disilicate with similar intensities were observed for both ceramics in the XRD analysis. Morphological analysis showed that the crystalline structure of the two ceramics studied showed no statistical difference after acid etching. Additionally, no significant differences were recorded in the number or size of the pores for the ceramics evaluated. Moreover, no differences in flexural strength were found for the ceramic materials tested, or in the bond strength to ceramic substrates for the resin cements. Based on the study results, no significant differences were found between the two CAD-CAM lithium disilicate glass-reinforced ceramics tested, since they presented similar crystalline structures with comparable intensities, and similar total porosity, flexural strength and bond strength.
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