Temperature effects on local structure, phase transformation, and mechanical properties of calcium silicate hydrates

被引:26
作者
Im, Sumin [1 ]
Jee, Hyeonseok [1 ]
Suh, Heongwon [1 ]
Kanematsu, Manabu [2 ]
Morooka, Satoshi [3 ]
Taku, Koyama [2 ]
Yuhei, Nishio [2 ]
Machida, Akihiko [4 ]
Kim, Jihoon [5 ]
Bae, Sungchul [1 ]
机构
[1] Hanyang Univ, Dept Architectural Engn, Seoul 04763, South Korea
[2] Tokyo Univ Sci, Fac Sci & Technol, Dept Architecture & Bldg Engn, Chiba, Japan
[3] Japan Atom Energy Agcy, Mat Sci Res Ctr, Ibaraki, Japan
[4] Natl Inst Quantum & Radiol Sci & Technol, Synchrotron Radiat Res Ctr, Sayo, Hyogo, Japan
[5] Muroran Inst Technol, Dept Civil Engn & Architecture, Muroran, Hokkaido, Japan
基金
新加坡国家研究基金会;
关键词
calcium– silicate– hydrate (C– S– H); deformation; heat treatment; local atomic arrangement; structure; X‐ ray methods; C-S-H; X-RAY-DIFFRACTION; THERMAL-STABILITY; PORE STRUCTURE; CEMENT PASTE; NMR; CONCRETE; RATIO; WOLLASTONITE; DISORDER;
D O I
10.1111/jace.17881
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This study aims to elucidate the effect of heating on the local atomic arrangements, structure, phase transformation, and mechanical properties of synthesized calcium-silicate-hydrate (C-S-H). The alteration in the atomic arrangement of the synthesized C-S-H (Ca/Si =0.8) and the formation of crystalline phases that occurred in three distinct transformation stages of dehydration (105 degrees C-200 degrees C), decomposition (300 degrees C-600 degrees C), and recrystallization (700 degrees C-1000 degrees C) were investigated via powder X-ray diffraction, Si-29 nuclear magnetic resonance spectroscopy, and thermogravimetric analysis. Further, the deformation of the local atomic bonding environment and variations in mechanical properties during the three stages were assessed via pair distribution function analysis based on in-situ total X-ray scattering. The results revealed that the C-S-H paste before heating exhibited a lower elastic modulus in real space than that in the reciprocal space in the initial loading stage because water molecules acted as a lubricant in the interlayer. At the dehydration stage, the strain as a function of external loading exhibited irregular deformation owing to the formation of additional pores induced by the evaporation of free moisture. At the decomposition stage, the structural deformation of the main d-spacing (d approximate to 3.0 A) was similar to that of the real space before the propagation of microcracks. At the recrystallization stage, the elastic modulus increased to 48 GPa owing to the thermal phase transformation of C-S-H to crystalline beta-wollastonite. The results provide direct experimental evidence of the microstructural and nanostructural deformation behavior of C-S-H pastes after exposure to high temperature under external loading.
引用
收藏
页码:4803 / 4818
页数:16
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