This paper presents an in-situ inspection and experimental investigation on the pore solution pH of concrete cover for the corrosion initiation of rebars under a long-term natural carbonation reaction. A 77-year-old steel mill was inspected, and 35 concrete column cover samples were collected to test the pH of the pore solution and phase compositions layer by layer. The variation in pH and phase compositions of the concrete along the cover depth was studied. The in-situ inspection results indicate that the rebar embedded in concrete had begun to corrode when the carbonation depth was almost less than one-third of the cover depth. The corrosion initiation of rebars embedded in concrete can occur when the pH is between 11.3 and 12.1. The pore solution pH test results and X-ray diffraction (XRD) analysis indicated that there is a semi-carbonated zone between the fully carbonated zone and the rebar. The pH of a fully carbonated zone is in a range of 8.0–9.5, and the pH of a semi-carbonated zone is between 9.5 and 12.1.
This paper presents an experimental investigation of the sulfuration mechanism of concrete. The microstructure, mineral phase composition, substance content, and pH of the concrete were determined using scanning electron microscopy, X-ray diffraction, comprehensive thermal analysis, and pore-solution pH test. It was observed that light-grey spots appeared on the surface of the specimen, and a large amount of powdery precipitated substances appeared. At the initial stage of sulfuration reaction, the formation of ettringite blocked the concrete pores and densified its cracks and voids. Subsequently, ettringite reacted with H+ to form gypsum, and the continuous increase in gypsum in the pores increased the number of cracks and broadened their width. Gypsum was the final product of the sulfuration reaction, and the mass percentage of gypsum in the powdery precipitated substances at different water–cement ratios was more than 50%. When the water–cement ratios was 0.37, 0.47, and 0.57, the highest Ca(OH)2 content was found for the lowest water–cement ratio. As the water–cement ratios increased, the amount of powdery precipitated substances decreased and the CaCO3 content and pH increased.
Iron and steel industry emits a large amount of CO2 and SO2 in the process of steelmaking, and these acid gases lead to the serious corrosion damage of concrete structures. In this paper, the environmental characteristics and corrosion degree of concrete in a 41-year-old steelworks were investigated, and the neutralization life prediction of the concrete structure was carried out. The results showed that the temperature, relative humidity, CO2 concentration, and SO2 concentration in the steelworks were 1.32, 0.62, 1.28, and 13.93 times higher than those of the general atmospheric environment, respectively. These environmental characteristics in various sections were significantly different. The appearance change of concrete in the ingot casting bay was more serious than that of concrete in the billet bay. Both the compressive strength of concrete in the ingot casting bay and billet bay decreased, and the strength in the billet bay was relatively low. The neutralization depth of concrete in the ingot casting bay was 2.35 times larger than that of concrete in the billet bay. The prediction model of concrete neutralization depth was established, and the remaining neutralization service life in the ingot casting bay and billet bay were 194.68 a and 202.07 a, respectively.
Iron and steel plants emit a large amount of CO2 and SO2 in the production process, and the high concentrations of acid gases lead to serious corrosion damage of concrete structures. In this paper, the environmental characteristics and corrosion damage degree of concrete in a 7-year-old coking ammonium sulfate workshop were investigated, and the neutralization life prediction of the concrete structure was carried out. Besides, the corrosion products were analyzed through concrete neutralization simulation test. The average temperature and relative humidity in the workshop were 34.7 °C and 43.4%, and they were 1.40 times higher and 1.70 times less than those of the general atmospheric environment, respectively. Both the concentrations of CO2 and SO2 were significantly different in various sections of the workshop, and they were much higher than those of the general atmospheric environment. The appearance corrosion and compressive strength loss of concrete were more serious in the sections with high SO2 concentration, such as vulcanization bed section and crystallization tank section. The neutralization depth of concrete in the crystallization tank section was the largest, with an average value of 19.86 mm. The corrosion products gypsum and CaCO3 were obviously visible in the surface layer of concrete, while only CaCO3 could be observed at 5 mm. The prediction model of concrete neutralization depth was established, and the remaining neutralization service life in the warehouse, synthesis section (indoor), synthesis section (outdoor), vulcanization bed section, and crystallization tank section were 69.21 a, 52.01 a, 88.56 a, 29.62 a, and 7.84 a, respectively.