Bae Sungchul, Taylor Rae, Kilcoyne David, Moon Juhyuk, Monteiro Paulo J M
Department of Architectural Engineering, Hanyang University, Seoul 04763, Korea.
Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720, USA.
Materials (Basel). 2017 Feb 4;10(2):131. doi: 10.3390/ma10020131.
This study assesses the quantitative effects of incorporating high-volume fly ash (HVFA) into tricalcium silicate (C₃S) paste on the hydration, degree of silicate polymerization, and Al substitution for Si in calcium silicate hydrate (C-S-H). Thermogravimetric analysis and isothermal conduction calorimetry showed that, although the induction period of C₃S hydration was significantly extended, the degree of hydration of C₃S after the deceleration period increased due to HVFA incorporation. Synchrotron-sourced soft X-ray spectromicroscopy further showed that most of the C₃S in the C₃S-HVFA paste was fully hydrated after 28 days of hydration, while that in the pure C₃S paste was not. The chemical shifts of the Si K edge peaks in the near-edge X-ray fine structure of C-S-H in the C₃S-HVFA paste directly indicate that Al substitutes for Si in C-S-H and that the additional silicate provided by the HVFA induces an enhanced degree of silicate polymerization. This new spectromicroscopic approach, supplemented with Al and Si magic-angle spinning nuclear magnetic resonance spectroscopy and transmission electron microscopy, turned out to be a powerful characterization tool for studying a local atomic binding structure of C-S-H in C₃S-HVFA system and presented results consistent with previous literature.
本研究评估了在硅酸三钙(C₃S)浆体中掺入大量粉煤灰(HVFA)对其水化、硅酸盐聚合程度以及硅酸钙水化物(C-S-H)中铝取代硅的定量影响。热重分析和等温传导量热法表明,虽然C₃S水化的诱导期显著延长,但由于掺入了HVFA,减速期后C₃S的水化程度增加。同步辐射源软X射线光谱显微镜进一步表明,C₃S-HVFA浆体中的大部分C₃S在水化28天后已完全水化,而纯C₃S浆体中的C₃S则未完全水化。C₃S-HVFA浆体中C-S-H的近边X射线精细结构中Si K边峰的化学位移直接表明,铝在C-S-H中取代了硅,并且HVFA提供的额外硅酸盐导致硅酸盐聚合程度增强。这种新的光谱显微镜方法,辅以铝和硅的魔角旋转核磁共振光谱以及透射电子显微镜,被证明是研究C₃S-HVFA系统中C-S-H局部原子结合结构的强大表征工具,其结果与先前文献一致。