Dynamic high‐temperature crystallization and processing properties of industrial soda–lime–silica glasses

液相线 方石英 材料科学 结晶 无定形固体 矿物学 相(物质) 衍射 分析化学(期刊) 石英 苏打石灰玻璃 过冷 化学工程 热力学 化学 光学 冶金 结晶学 复合材料 合金 物理 有机化学 色谱法 工程类
作者
Erhan Kilinc,A.M.T. Bell,Paul A. Bingham
出处
期刊:Journal of the American Ceramic Society [Wiley]
卷期号:107 (4): 2242-2259 被引量:2
标识
DOI:10.1111/jace.19602
摘要

Abstract In situ dynamic crystallization properties of industrial soda–lime–silica glasses at realistic processing temperatures have not yet been explored. Hence, we collected in situ high‐temperature X‐ray diffraction patterns for 10 different industrially manufactured soda–lime–silica glasses as a function of temperature between 900 and 1200°C to investigate the phase relations in their devitrified melts. The high‐temperature X‐ray diffraction study was complemented by measuring the liquidus temperature of those glasses by the temperature gradient technique. A multiple variable regression analysis was applied to the experimental and modeled data to produce a predictive model for the rate of solidification and liquidus temperature based on glass composition. We have demonstrated that forms of quartz (SiO 2 ) and Na 2 CaSiO 4 , which are not traditionally identified by room temperature X‐ray diffraction studies of commercial soda–lime–silica glasses, are the dominant crystalline phases at 800 and 900°C. Upon further heating, different forms of cristobalite become the primary phase field prior to the formation of X‐ray amorphous melts, irrespective of the glass composition. Sporadic unidentified as well as high‐temperature stable SiO 2 polymorphs that are not recoverable to room temperature were also observed. In contrast to the literature, wollastonite (CaSiO 3 ) and devitrite (Na 2 Ca 3 Si 6 O 16 ), which are the main predictor variables in previously developed liquidus temperature models, were not observed prior to the formation of X‐ray amorphous glass melts, and hence their influence on liquidus temperature may be questionable. It was also found that the difference between glass processing and liquidus temperatures can be excessively high, and such large temperature differences can potentially be exploited and reduced to enable decreases in melting or processing temperatures of industrial soda–lime–silica glass melts.
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