Microstructure and characterization of hydrothermal synthesis of Al-substituted tobermorite

被引:62
|
作者
Guo, Xiaolu [1 ,2 ]
Meng, Fanjie [2 ]
Shi, Huisheng [1 ,2 ]
机构
[1] Tongji Univ, Minist Educ, Key Lab Adv Civil Engn Mat, Shanghai 201804, Peoples R China
[2] Tongji Univ, Sch Mat Sci & Engn, 4800 Caoan Rd, Shanghai 201804, Peoples R China
基金
中国国家自然科学基金;
关键词
Tobermorite; Aluminum; Hydrothermal synthesis; Microstructure; C-S-H; BLAST-FURNACE SLAG; SI-29; NMR; AL-27; SPECTROSCOPY; ALUMINUM; SOLIDIFICATION; PHASES; ASH;
D O I
10.1016/j.conbuildmat.2016.12.059
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Tobermorite is an important mineral analog of calcium silicate hydrate (C-S-H), the main phase formed by hydration of Portland cement, due to the structural similarity. As part of a broader study on the effect of aluminum substitution C-S-H, the synthesis and characterization of tobermorite with and without aluminum were conducted. The X-ray diffraction pattern indicated that a suitable synthesis time for tobermorite with or without aluminum was 5 h in an autoclave at 180 degrees C and Saturated steam pressure around 1 MPa. In both samples the mineral is 11 angstrom-tobermorite. X-ray fluorescehce showed that the sample with aluminum had a higher molar ratio of Ca/(Si + Al). Thermogravimetry-differential scanning calorimetry showed the same general changes, loss of free water at 55 degrees C, loss of interlayer water at 187 degrees C, dehydroxylation at 664 degrees C, and conversion to wollastonite at 841 C. With the incorporation of aluminum, 29Si and 27Al magic angle spinning-nuclear magnetic resonance spectra showed aluminum addition increases the mean chain length, Al mainly occupies Q(2) bridging and Q(3) branching sites. Scanning electron Micrographs indicated that tobermorite crystals are larger than those of sample without alumina. This work is beneficial for understanding the implication of the use of admixtures containing aluminum in concrete on its micro- and atomic-scale properties. (C) 2016 Published by Elsevier Ltd.
引用
收藏
页码:253 / 260
页数:8
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