Coordination environment of Si in calcium silicate hydrates, silicate minerals, and blast furnace slags: A XANES database

被引:35
作者
Li, Jiaqi [1 ]
Zhang, Wenxin [1 ]
Garbev, Krassimir [2 ]
Monteiro, Paulo J. M. [1 ]
机构
[1] Univ Calif Berkeley, Dept Civil & Environm Engn, Berkeley, CA 94720 USA
[2] Karlsruhe Inst Technol, Inst Tech Chem, D-76021 Karlsruhe, Germany
基金
新加坡国家研究基金会;
关键词
XANES; X-ray absorption spectra; C-S-H; Tobermorite; Silicate polymerization; CRYSTAL-STRUCTURE; TRICALCIUM SILICATE; CEMENT; FIELD; AL; SPECTROSCOPY; TEMPERATURE; MORPHOLOGY; CHEMISTRY; PRODUCTS;
D O I
10.1016/j.cemconres.2021.106376
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Understanding the silicate polymerization of calcium silicate hydrate (C-S-H) gel and its crystalline polymorphs is important in cement science. NMR can determine Si environments, but the measurement can be time-consuming and provides no spatial information. X-ray absorption near-edge structure (XANES) spectroscopy is a fast tool for probing Si coordination, possibly with spatial information. However, there lacks an understanding of Si K-edge XANES spectra of cement-related silicate phases. Here, a Si K-edge XANES spectral database of nanocrystalline C-S-H, C-S-H minerals, blast-furnace slags, and metakaolin is provided. Si K-edge of C-S-H minerals shifts to higher energies with higher polymerized Si and lower Ca-Si connectivity in the Si second nearest neighbor shell. Si K-edge energy shows weak correlations with Ca/Si ratio, average Si-O bond length, and SiO4 distortion due to the structural complexity of silicates. The substitution of Al for Si shifts the Si K-edge of tobermorite and slags to higher energies.
引用
收藏
页数:13
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