In this paper, the microstructure and resistance to chloride ion penetration of ultra-high-performance concrete (UHPC) prepared from lightweight aggregate (LWA) were studied through simulation and experiment. The effects of LWA with different particle sizes on the chloride ion transport properties of lightweight ultra-high-performance concrete (L-UHPC) were discussed through simulation test results. The random delivery model of LWA in L-UHPC was established by MATLAB, and the model was introduced into COMSOL. Through the comparative analysis of experimental data and simulation results, the repeatability of the proposed model and the simulation accuracy were verified. The results show that when the LWA particle size changes from 0.15–4.75 mm to 0.15–1.18 mm, the width of interfacial transition zone (ITZ) and the overall porosity of L-UHPC decrease. This is because the large particle size LWA has more open pores with larger pore diameters and related interconnections, which are potential channels for chloride ion transport. Therefore, the chloride ion transport properties in L-UHPC are inhibited, which is manifested by the “tortuosity effect” of the LWA.

Chloride ion corrosion of steel bars is one of the important reasons for the decline of durability and service life of concrete structures. Due to the complexity of concrete structure, the migration process of chloride ions in concrete is diversified. Therefore, it is difficult to show the transport mechanism of chloride ions in concrete by a single experimental study. It is necessary to explore the transmission process and mechanism of chloride ions in concrete through theoretical simulation on the basis of experimental research. This paper summarizes the relevant models and methods of chloride transport, points out the advantages and disadvantages of existing models, and prospects the research direction of chloride transport models.

The durability of C₃S-C₃A paste with varied C₃A content (0%, 5%, 10%, and 20%) against sulfate attack at various attack ages (3 d, 7 d, 28 d, and 180 d) was investigated in this study through the examinations of corrosion product composition, Ca/Si and Al/Si of calcium-(aluminum)-silicate-hydrate (C-(A)-S-H) gel, formation and evolution of microstructure, migration and transformation of Al containing phase products, and pore structure. The results indicated that sulfate attack can promote the hydration reaction in C₃S-C₃A paste, thus accelerating the production of C-(A)-S-H gel in the paste. With the increase of C₃A content, the acceleration effect becomes more significant. In addition, sulfate attack led to the dealumination and decalcification of C-(A)-S-H gel, resulting in the reduction of the gelling power of C-(A)-S-H gel. The degree of dealumination and decalcification of C-(A)-S-H gel increases with the increase of C3A content. At the same time, free Al and Ca promote the formation of expansive products such as ettringite and gypsum. Finally, under the action of sulfate, the pore characterization of C₃S-C₃A paste deteriorated, showing a decrease in specific surface area, cumulative pore volume and average pore diameter.