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Building materials are constantly improved with various additives and admixtures in order to achieve goals ranging from obtaining increased durability or antimicrobial activity up to reducing the carbon footprint left by the cement production. Since nanomaterials were proposed for cement products, many studies explored the possibilities for their incorporation. One of the novel trends in studying these materials is evaluating their impact on living organisms, with the focus not only on toxicology but also on the application potential. Therefore, in this study, we investigated the effects of three types of calciumsilicate-hydrate (C-S-H) seeds on reference microorganisms in the scope of their basic physiology and primary metabolism. Shape, size and elemental composition of C-S-H seeds were also evaluated. The tests on the reference microorganisms have shown that the reaction to these nanomaterials can be specific and depends on the strain as well as the type of used nanomaterial. Furthermore, the presence of C-S-H seeds in the growth environment led to metabolic stimulation that resulted in faster growth, higher biochemical activity, and increased biofilm formation. Based on our findings, we conclude that even though C-S-H seeds have antimicrobial potential, they can be potentially used to promote the growth of selected microbial strains. This phenomenon could be further investigated towards the formation of beneficial biofilms on building materials.

In the current study, the development of the silicate structure of synthetic calcium silicate hydrates with different calcium contents were followed by in-situ infrared (IR) spectroscopy and correlated to the in-situ phase development evaluated by X-ray diffraction (XRD). A baseline correction method initially developed for X-ray diffractograms was successfully adapted for the complex background of the fingerprint region in in-situ IR, which significantly contributed to signal quality and reproducibility. The development of separate silicate infrared bands could be monitored over 24 h of reaction. These bands could be assigned to oligomeric and dimeric species based on their time and stoichiometry dependent development. It was clearly shown that the main peak of the dimeric silicate species was overlooked in the literature. The correlation of time-dependent events to in-situ XRD revealed that changes in the unit cell of calcium silicate hydrate are related to silicate polymerisation.

In this article the progress of the research on cement hydration mechanisms is critically reviewed, starting with the work of Le Chatelier and Michaelis during the late nineteenth century. Proposed mechanisms are discussed in the light of experimental data to highlight the role of new or improved analytical techniques. The focus of this article lies on the dormant period and the silicate reaction. Today many of the mechanisms proposed throughout time cannot withstand experimental evidence and need to be rejected, including the classical protective hydrate layer theory. However, it seems likely that hydrated surface species are involved in the mechanism. Theories that aim to explain the rate changes solely based on the nucleation and growth of portlandite can also not withstand experimental evidence. Nevertheless, the retardation of portlandite crystal growth through silicate ions is a relevant factor. Especially since it might present a mechanism for the nucleation of calcium silicate hydrate (C–S–H), backing up theories that propose C–S–H and portlandite to grow from the same nuclei. Finally, an overview over facts, that are currently considered to be valid and hence need to be regarded in the future mechanisms is given.