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Early Age Carbonation Heat and Products of Tricalcium Silicate Paste Subject to Carbon Dioxide Curing

机译:二氧化碳固化后的早期碳化热和硅酸三钙膏产品

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摘要

This paper presents a study on the carbonation reaction heat and products of tricalcium silicate (C3S) paste exposed to carbon dioxide (CO2) for rapid curing. Reaction heat was measured using a retrofitted micro-calorimeter. The highest heat flow of a C3S paste subject to carbonation curing was 200 times higher than that by hydration, and the cumulative heat released by carbonation was three times higher. The compressive strength of a C3S paste carbonated for 2 h and 24 h was 27.5 MPa and 62.9 MPa, respectively. The 24-h carbonation strength had exceeded the hydration strength at 28 days. The CO2 uptake of a C3S paste carbonated for 2 h and 24 h was 17% and 26%, respectively. The X-ray diffraction (XRD), transmission electron microscope coupled with energy dispersive spectrometer (TEM-EDS), and 29Si magic angle spinning–nuclear magnetic resonance (29Si MAS-NMR) results showed that the products of a carbonated C3S paste were amorphous silica (SiO2) and calcite crystal. There was no trace of calcium silicate hydrate (C–S–H) or other polymorphs of calcium carbonate (CaCO3) detected.
机译:本文介绍了碳化反应热和硅酸三钙(C3S)糊状物暴露于二氧化碳(CO2)以快速固化的产物的研究。使用改进的微量量热计测量反应热。进行碳化固化的C3S浆料的最高热流率比水合作用时高200倍,而碳化所释放的累积热量高出三倍。碳酸化2 h和24 h的C3S糊的抗压强度分别为27.5 MPa和62.9 MPa。 24小时碳酸化强度超过28天时的水合强度。碳酸化2小时和24小时的C3S糊剂的CO2吸收分别为17%和26%。 X射线衍射(XRD),透射电子显微镜和能量色散仪(TEM-EDS)以及 29 Si幻角旋转核磁共振( 29 Si MAS-NMR)结果表明,碳酸盐化的C3S糊状物为无定形二氧化硅(SiO2)和方解石晶体。没有发现水合硅酸钙(C–S–H)或碳酸钙(CaCO3)的其他多晶型物的痕迹。

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