Microstructure of Carbonation-Activated Steel Slag Binder

被引:25
|
作者
Ghouleh, Zaid [1 ]
Celikin, Mert [2 ]
Guthrie, Roderick I. L. [2 ]
Shao, Yixin [1 ]
机构
[1] McGill Univ, Dept Civil Engn, 817 Sherbrooke St West, Montreal, PQ H3A 2K6, Canada
[2] McGill Univ, Dept Mat Engn, 3610 Univ St, Montreal, PQ H3A 0C5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Carbonation; Di-calcium-silicates; Microstructure; Transmission electron microscope (TEM); Calcium-silicate-hydrate (C S H); Nanocomposites; C-S-H; RAMAN-SPECTROSCOPY; MICRO-RAMAN; PART II; CALCIUM SILICATES; LONG-TERM; CEMENT; HYDRATION; BEHAVIOR; DIOXIDE;
D O I
10.1061/(ASCE)MT.1943-5533.0002421
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
A steel slag material demonstrated rapid hardening and a considerable gain in compressive strength upon reacting with carbon dioxide. Two-hour carbonated paste compacts achieved an average compressive strength of 80MPa, warranting the slag's consideration as a cement-like binder for building applications. The microstructure of this CO2-activated binder system was examined. The reaction was found to engage the di-calcium-silicate component of the slag to generate a hardened matrix consisting of CaCO3 and a low-lime calcium-silicate-hydrate (C S H) phase. The latter differed in composition and structure from C S H variants generated from normal portland cement hydration. Raman spectroscopy confirmed bands (330, 510-550, 600-630, and 1,005cm-1) consistent with C S H species having low-lime compositions. High-resolution transmission electron microscope (TEM) resolved lamellar features for C S H with short basal spacings (averaging 0.73nm), correlatively indicating superior interlayer cohesion. Moreover, abundant nano-CaCO3 crystals were found interlocked within the C S H phase, forming a dense nanoscale composite matrix. Such a proposed binder system is completely by-product-sourced, thus presenting the potential of eliminating or significantly reducing the carbon footprint of building products.
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页数:11
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