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将大量粉煤灰掺入硅酸三钙中对硅酸盐水合物中硅聚合度及硅的铝取代的影响

Effects of Incorporating High-Volume Fly Ash into Tricalcium Silicate on the Degree of Silicate Polymerization and Aluminum Substitution for Silicon in Calcium Silicate Hydrate.

作者信息

Bae Sungchul, Taylor Rae, Kilcoyne David, Moon Juhyuk, Monteiro Paulo J M

机构信息

Department of Architectural Engineering, Hanyang University, Seoul 04763, Korea.

Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720, USA.

出版信息

Materials (Basel). 2017 Feb 4;10(2):131. doi: 10.3390/ma10020131.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d929/5459114/8d2ee355d423/materials-10-00131-g001.jpg

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