结晶
材料科学
方石英
差示扫描量热法
微观结构
扫描电子显微镜
锂(药物)
矿物学
化学工程
降水
陶瓷
分析化学(期刊)
复合材料
化学
热力学
物理
工程类
内分泌学
气象学
色谱法
石英
医学
作者
Sascha Cramer von Clausbruch,Marcel Schweiger,Wolfram Höland,Volker Rheinberger
标识
DOI:10.1016/s0022-3093(99)00647-x
摘要
Abstract Six glasses in the SiO 2 –Li 2 O–K 2 O–ZnO–P 2 O 5 system were prepared, varying the P 2 O 5 content from 0.0 to 2.5 mol% with the molar ratios of the other components being invariant. Crystallization processes of these glasses were investigated using high temperature XRD and differential scanning calorimetry. Morphology and microstructure of the glass-ceramics were studied using scanning electron microscopy. Crystallization of these glasses occurred in the temperature range 500–750°C. The main crystalline phase was lithium disilicate (Li 2 Si 2 O 5 ). Lithium metasilicate, lithium orthophosphate and cristobalite were secondary phases. In glasses with a P 2 O 5 content of more than 1.0 mol%, precipitation of cristobalite took place prior to the main crystallization of lithium disilicate. Surface crystallization occurred in glasses with a P 2 O 5 content of 0.0 and 0.5 mol%. Furthermore, a spherulitic morphology of lithium disilicate crystals in the interior of the samples was observed. Lithium disilicate crystals in glasses with a P 2 O 5 content of 1.0–2.5 mol% had an elongated shape along the c -axis, a crystal length ranging from 1 to 5 μm and aspect ratios between 2 and 6. Rod-shaped crystals were randomly oriented in the volume of the glass-ceramics and were responsible for the mechanical strength of up to 440 MPa.
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