Prabhu Achutha, Gimel Jean-Christophe, Ayuela Andrés, Arrese-Igor Silvia, Gaitero Juan J, Dolado Jorge S
División de Construcción Sostenible, TECNALIA, Parque Tecnológico de Bizkaia, Astondo Bidea, Edificio 700, 48160, Derio, Spain.
MINT, UNIV Angers, INSERM 1066, CNRS 6021, Université Bretagne Loire, IBS-CHU, 4 rue Larrey, 49933, Angers, France.
Sci Rep. 2018 Oct 25;8(1):15830. doi: 10.1038/s41598-018-33918-6.
Shortly after mixing cement grains with water, a cementitious fluid paste is formed that immediately transforms into a solid form by a phenomenon known as setting. Setting actually corresponds to the percolation of emergent network structures consisting of dissolving cement grains glued together by nanoscale hydration products, mainly calcium-silicate-hydrates. As happens in many percolation phenomena problems, the theoretical identification of the percolation threshold (i.e. the cement setting) is still challenging, since the length scale where percolation becomes apparent (typically the length of the cement grains, microns) is many times larger than the nanoscale hydrates forming the growing spanning network. Up to now, the long-lasting gap of knowledge on the establishment of a seamless handshake between both scales has been an unsurmountable obstacle for the development of a predictive theory of setting. Herein we present a true multi-scale model which concurrently provides information at the scale of cement grains (microns) and at the scale of the nano-hydrates that emerge during cement hydration. A key feature of the model is the recognition of cement setting as an off-lattice bond percolation process between cement grains. Inasmuch as this is so, the macroscopic probability of forming bonds between cement grains can be statistically analysed in smaller local observation windows containing fewer cement grains, where the nucleation and growth of the nano-hydrates can be explicitly described using a kinetic Monte Carlo Nucleation and Growth model. The most striking result of the model is the finding that only a few links (~12%) between cement grains are needed to reach setting. This directly unveils the importance of explicitly including nano-texture on the description of setting and explains why so low amount of nano-hydrates is needed for forming a spanning network. From the simulations, it becomes evident that this low amount is least affected by processing variables like the water-to-cement ratio and the presence of large quantities of nonreactive fillers. These counter-intuitive predictions were verified by ex-professo experiments that we have carried out to check the validity of our model.
将水泥颗粒与水混合后不久,会形成一种水泥质流体浆体,该浆体通过一种称为凝结的现象立即转变为固体形态。凝结实际上对应于由溶解的水泥颗粒通过纳米级水化产物(主要是硅酸钙水合物)粘结在一起形成的新兴网络结构的渗流。正如许多渗流现象问题一样,渗流阈值(即水泥凝结)的理论确定仍然具有挑战性,因为渗流变得明显的长度尺度(通常是水泥颗粒的长度,微米级)比形成不断增长的跨越网络的纳米级水合物大很多倍。到目前为止,在两个尺度之间建立无缝衔接方面长期存在的知识空白一直是发展凝结预测理论的不可逾越的障碍。在此,我们提出了一个真正的多尺度模型,该模型同时在水泥颗粒尺度(微米级)和水泥水化过程中出现的纳米水合物尺度上提供信息。该模型的一个关键特征是将水泥凝结识别为水泥颗粒之间的非晶格键渗流过程。既然如此,就可以在包含较少水泥颗粒的较小局部观察窗口中对水泥颗粒之间形成键的宏观概率进行统计分析,在这些窗口中,可以使用动力学蒙特卡洛成核与生长模型明确描述纳米水合物的成核和生长。该模型最引人注目的结果是发现仅需水泥颗粒之间的少数连接(约12%)就能达到凝结。这直接揭示了在凝结描述中明确纳入纳米结构的重要性,并解释了为什么形成跨越网络所需的纳米水合物量如此之少。从模拟中可以明显看出,这个低量受水灰比和大量非活性填料等加工变量的影响最小。我们通过专门实验验证了这些与直觉相悖的预测,以检验我们模型的有效性。