ABSTRACT
The structural systems of residential buildings in many developed countries have widely utilized reinforced concrete as the most common solution in construction systems since the early 20th century. The durability of reinforced concrete columns and beams is compromised, in most cases, by pathologies caused by the corrosion of their reinforcements. This study analyses the corrosion processes induced by carbonation in 25 buildings with reinforced concrete structures. The models estimate the service life of reinforced concrete elements by differentiating between the initiation period and the propagation period of damage, considering two possible stages: the time of corrosion propagation until the cracking of the concrete cover, and the time of propagation until a loss of section is considered unacceptable for structural safety. However, the mathematical expressions that model the propagation periods consider the same corrosion rate in both cases. This research has found that the average corrosion rate in elements with an unacceptable loss of reinforcement section was in the order of 8 times higher than the corrosion rate in cracked columns and beams without a loss of reinforcement. This opens up a path to improve the definition of the different stages experienced by a reinforced concrete element suffering corrosion of its reinforcements due to carbonation, because once the concrete has cracked, the corrosion rate increases significantly.
ABSTRACT
To ensure that a structure will last throughout its service life, repairing reinforced concrete entails, among others, correctly marking off the area affected by aggressive agents that may deteriorate both the concrete and the steel. Chloride, the most damaging source of reinforcement corrosion, may diffuse to a greater or lesser distance from the surface depending on the ease of penetration. In this study, we calibrated a handheld X-ray fluorescence analyser (hXRF) and used it to quantify the chloride concentration in cement-based materials. The findings were verified against a series of samples of known concentration to establish a suitable correction factor. Chloride ions were quantified precisely and accurately with the hXRF instrument, and we calculated a correction factor of 1.16. The instrument and the information recorded were used to quantify the chloride ion content in different parts of an existing structure. The analyser identified apparently healthy areas that could, nonetheless, pose oxidation problems in the near future due to significant chloride concentration. Chloride quantification data at different depths can be used to draw diffusion or penetration profiles and to determine whether ion concentration around the reinforcement is within the recommended limits. The method developed can be applied in situ to quickly locate the most critical areas.
