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Study of the Non-Isothermal Crystallization Kinetics of Lithium Disilicate Glass Ceramic

机译:锂大胆玻璃陶瓷非等温结晶动力学的研究

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摘要

The glass ceramic with the crystals of lithium disilicate Li2O 2SiO(2) (LS2) as the main crystal phase is one of the prospective materials in the field of restorative dentistry. In this study, the crystallization kinetics of LS2 glass ceramic obtained from the base glass of the system SiO2-Li2O-Al2O3-K2O-P2O5 were investigated by the non-isothermal method using differential thermal analysis at four different heating rates. The DTA curves showed different exothermic crystallization peaks over the temperature ranges of 645-683 and 807-845 degrees C. The lithium metasilicate, Li2O SiO 2 (LS), and the lithium disilicate, crystallized over these respective temperature ranges, was established by XRD technique. The crystallization kinetic parameters were calculated by the Kissinger plot and Augis-Bennett equations for non-isothermal analysis. The calculated activation energy of crystal growth, E-C1= 236 kJ/mol, E-C2 = 340 kJ/mol, and the Avrami parameters, n(1) = 1.46-1.67, n(2) = 2.73-2.91, together with the results from SEM observations, indicated that the crystallization mechanism of LS was substantial surface crystallization while the crystallization mechanism of LS2 was dominant bulk crystallization. The calculated activation energy of glass transition was also determined E-V= 516kJ/mol.
机译:玻璃陶瓷与锂锂锂晶晶Li 2 O 2 SiO(2)(LS2)为主要晶相是恢复牙科领域的预期材料之一。在这项研究中,LS2玻璃的结晶动力学陶瓷从系统中通过使用差示热分析在四个不同的加热速率的非等温方法SiO 2系的Li2O-Al2O3的-K2O-P2O5进行了调查的基础玻璃而获得。 DTA曲线在645-683和807-845℃的温度范围内显示出不同的放热结晶峰。通过XRD建立了锂偏离锂偏析,Li 2 O SiO 2(LS)和锂峰结晶,并通过XRD建立技术。结晶动力学参数由Kissinger Plot和Augis-Bennett方程计算出非等温分析。晶体生长的计算活化能,E-C1 = 236 kJ / mol,E-C2 = 340 kJ / mol,以及Avrami参数,n(1)= 1.46-1.67,n(2)= 2.73-2.91,在一起随着SEM观察结果的结果,表明LS的结晶机制是显着的表面结晶,而LS2的结晶机理是显性散装结晶。还测定了玻璃转变的计算的激活能量E-V = 516kJ / mol。

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