Protective carrier is essential for the self‐healing of concrete cracks by microbially induced CaCO₃ precipitation, owing to the harsh conditions in concrete. In this paper, porous ceramsite particles are used as microbial carrier. Heat treatment and NaOH soaking are first employed to improve the loading content of the ceramsite. The viability of bacterial spores is assessed by urea decomposition measurements. Then, the self‐healing efficiency of concrete cracks by spores is evaluated by a series of tests including compressive strength regain, water uptake, and visual inspection of cracks. Results indicate that heat treatment can improve the loading content of ceramsite while not leading to a reduction of concrete strength by the ceramsite addition. The optimal heating temperature is 750°C. Ceramsite particles act as a shelter and protect spores from high‐pH environment in concrete. When nutrients and spores are incorporated in ceramsite particles at the same time, nutrients are well accessible to the cells. The regain ratio of the compressive strength increases over 20%, and the water absorption ratio decreases about 30% compared with the control. The healing ratio of cracks reaches 86%, and the maximum crack width healed is near 0.3 mm.

The lack of river sand is becoming increasingly serious. In this study, we consider how to use sea sand to prepare innovative construction and building materials with excellent mechanical and durability properties. Sulphate corrosion causes expansion, cracking and spalling of concrete, resulting in the reduction or even loss of concrete strength and cementation force. In this paper, artificial seawater, sea sand, industrial waste, steel fiber and polycarboxylate superplasticizer were used to prepare ultra-high-performance polymer cement mortar (SSUHPC), and the sulphate corrosion mechanism was investigated. The strength and cementation force of mortar on the SSUHPC surface decreased and flaked off with the development of sulphate erosion, and the steel fiber rusted and fell off. A 3D model was established based on X-ray computed tomography (X-CT), and the results showed that SSUHPC maintained excellent internal structural characteristics despite severe sulphate erosion on the surface. Mercury intrusion porosimetry (MIP), scanning electron microscopy (SEM) and X-ray diffraction (XRD) techniques were adopted to investigate the sulphate corrosion mechanism of SSUHPC. We found a transition zone within 1–5 mm of the surface of SSUHPC. The Vickers hardness of mortar in this area was increased by 5~15%, and the porosity was reduced to 3.8489%. Obvious structural damage did not occur in this area, but a high content of gypsum appeared. UHPC prepared with seawater sea sand was found to have better sulphate resistance than that prepared with freshwater river sand, which supports the development and utilization of sea sand in concrete.

Due to its special two-dimensional lamellar structure, graphene possesses an excellent shielding effect, hydrophobic characteristics and large specific surface area, which can effectively isolate the internal structure from the external corrosive media. However, lamellar graphene is easy to stack and agglomerate, which limits its anti-corrosion performance. In this paper, cerium oxide-graphene oxide (CeO₂-GO) nanocomposites were prepared by a hydrothermal synthesis method. Field emission scanning electron microscope (FESEM) and transmission electron microscope (TEM) were applied for microstructure examination, showing that a large number of nanoscale granular cerium oxide grew on the lamellar graphene oxide surface, which improved the dispersion performance of graphene inside the matrix. The anti-corrosion properties of the coating were analyzed and illustrated by open circuit potential (OCP), frequency response analysis, Tafel curve and Mott–Schottky curve. The results indicated that the CeO₂-GO (4:1) nanocomposite not only eliminated the agglomeration of graphene to some extent, but also prepared the graphene epoxy coating with good dispersion, which further promoted its anti-corrosion performance. The paper proposed a feasible solution for GO dispersion in cement-based materials and lays a solid theoretical foundation for the engineering application of cerium oxide-graphene oxide modified anticorrosive coating.

This paper presents an experimental investigation on the effect of nano-montmorillonite, carbon nanotubes, and nano calcium carbonate on autogenous shrinkage of cement based materials. Cement paste with different nano-montmorillonite dosage (1.0 wt.%, 2.0 wt.%, 3.0 wt.%), carbon nanotubes dosage (0.1 wt.%, 0.2 wt.%, 0.3 wt.%), and nano calcium carbonate dosage (1.0 wt.%, 2.0 wt.%, 3.0 wt.%) were compared with the reference group to assess the effects of nano-materials on cement paste. Results show that autogenous shrinkage of cement based materials containing nano-materials mainly occurs in the first 72 h. Nano-materials decrease the autogenous shrinkage of the investigated cement based materials at all ages. Compared with that of the reference group at the age of 168 h, the autogenous shrinkage of NM-modified cement based composites containing 3.0 wt.% NM decreased by as much as 57.4%; the autogenous shrinkage of CNTs-modified cement based composites containing 0.3 wt.% CNTs decreased by as much as 19.4%; the autogenous shrinkage of NC-modified cement based composites containing 2.0 wt.% NC decreased by as much as 17.1%. Electrochemical AC (Alternating Current) impedance spectroscopy results show that the resistance of the pore solution electrolyte of specimens containing nano-materials increases with age, and is less than that of specimens without nano-materials, which illustrates that the pore size of nano-modified cement based material is finer and autogenous shrinkage is smaller. Scanning electron microscope results show that the structure of cement matrix is denser with more hydration products by adding nano-materials. Nano-montmorillonite releases water to reduce self-drying effect during the process of hydration for its well water swelling. Carbon nanotubes have the nanometer filling effect and form a continuous network to restrain the early autogenous shrinkage of cement paste. Nano calcium carbonate not only decreases the porosity of the cement paste, but also reacts with tricalcium aluminate to generate the expanded product calcium carboaluminate for compensating autogenous shrinkage of cement paste.