水镁石
成核
水合硅酸钙
镁
热重分析
硅酸盐
水合物
溶解
硅粉
动力学
扫描电子显微镜
化学工程
材料科学
化学
核化学
矿物学
结晶学
水泥
物理化学
有机化学
冶金
物理
工程类
复合材料
量子力学
作者
Marco Simoni,Chun Long Woo,Han Zhao,Dinu Iuga,Petr Svora,Theodore Hanein,Hajime Kinoshita,Brant Walkley
标识
DOI:10.1016/j.cemconres.2023.107295
摘要
M-S-H gels were synthesised via reaction of Mg(OH)2 with silica fume, cured at 35 °C for up to 112 days, and their chemical and nanostructural evolution was examined. M-S-H gels with structural similarity to the thermodynamically stable serpentine-group mineral lizardite were formed. Quantification of 25Mg and 29Si MAS and 1H29Si CPMAS NMR, electron microscopy, and thermogravimetric data showed dissolution of brucite and silica fume, and M-S-H formation, all occurred linearly with time up to 56 days. Data showed strong correlation with the Avrami-Erofeyey nucleation kinetic model, indicating M-S-H formation was governed by nucleation reactions. After 112 days, two distinct M-S-H gels were formed: a Si-rich M-S-H gel with molar Mg/Si = 0.55(±0.2), and a Mg-rich M-S-H gel with molar Mg/Si = 0.80(±0.5). Nanostructural rearrangement of M-S-H continues up to 112 days, with increased crosslinking and polymerisation. This new insight is important for application of M-S-H binders in both construction and radioactive/toxic waste immobilisation.
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