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Hydration of a ternary binder model system and the influence of citric acid on phase evolution

机译:三元黏合剂模型体系的水合及柠檬酸对相演化的影响

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Ternary-binder-like mixes were prepared from synthesized calcium aluminates CA and C_3A, which represent calcium aluminate cement and silicate-free OPC, together with calcium sulfates. The CA-C_3A-Ca-sulfate mixes were investigated with respect to the question of the influence of citric acid on hydration and ettringite formation. For better comparison of the technical with the model system an inert filler was added to be able to use similar w/s ratios and citric acid concentrations as for technical applications. The interesting calcium sulfates, bassanite und anhydrite II, were synthesized from gypsum by temperature-dependent dehydration processes. The cement phases CA and C_3A were synthesized from CaCO_3 and α-Al_2O_3 at 1400°C and ground to an appropriate specific surface area (Blaine 3800 resp. 4700 cm~2/g). The obtained data were refined by Rietveld analysis. During hydration of the mixes with pure H_2O ettringite and minor amounts of monosulfate 14-hydrate are forming. A low amount of 0.1 wt% citric acid in the mixing water leads to more precipitated ettringite during the first 15 min. After the initial hydration of the ternary binder model mix more C_3A is found to be dissolved. But then the dissolution of C_3A is not proceeding until 2 h of hydration and then continues again until 3 h. The dissolution of CA is only little affected when citric acid is dissolved in the mixing water. Bassanite cannot be detected in the pastes after mixing nor with H_2O neither in the citric acid containing solution. Kinetics of ettringite formation is strongly influenced by the presence of citric acid in contrast to its formation in pure H_2O. After 3 h the maximum ettringite content is reached with citric acid. In comparison the maximum ettringite for pure H_2O solution was already reached after 1.5 h. This shows that citric acid is acting as an accelerator during the initial hydration and as a retarder between 15 min and 3 h.
机译:由代表铝酸钙水泥和不含硅酸盐的OPC的合成铝酸钙CA和C_3A以及硫酸钙制备了三元粘合剂状混合物。针对柠檬酸对水合和钙矾石形成的影响问题,研究了CA-C_3A-Ca-硫酸盐混合物。为了更好地将技术与模型系统进行比较,添加了惰性填料,以便能够使用与技术应用类似的w / s比和柠檬酸浓度。有趣的硫酸钙,重钙锌矿和无水石膏II,是通过依赖于温度的脱水过程从石膏中合成的。水泥相CA和C_3A是在1400°C下由CaCO_3和α-Al_2O_3合成的,并研磨至合适的比表面积(Blaine 3800分别为4700 cm〜2 / g)。通过Rietveld分析对获得的数据进行精炼。在与纯H_2O钙矾石的混合物水合期间,形成了少量的单硫酸盐14水合物。在最初的15分钟内,混合水中少量的0.1 wt%柠檬酸会导致沉淀的钙矾石更多。在三元粘合剂模型混合物初始水合后,发现更多的C_3A溶解了。但是,直到水合2小时才开始进行C_3A的溶解,然后再继续溶解直到3小时。当柠檬酸溶解在混合水中时,CA的溶解几乎不会受到影响。混合后无法在糊剂中检测到Bassanite,也无法在含柠檬酸的溶液中检测到H_2O。柠檬酸的形成动力学受柠檬酸的存在的强烈影响,与柠檬酸在纯H_2O中的形成相反。 3小时后,柠檬酸达到最大钙矾石含量。相比之下,纯水H_2O溶液的最大钙矾石在1.5小时后就已经达到。这表明柠檬酸在初始水合过程中起促进剂的作用,在15分钟至3小时之间起缓凝剂的作用。

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