Study on Concrete Deterioration in Different NaCl-Na2SO4 Solutions and the Mechanism of Cl− Diffusion

• Published in: Materials Vol. 14; no. 17; p. 5054
• Main Authors: Zhang, Fei, Hu, Zhiping, Wei, Feng, Wen, Xin, Li, Xiaoguang, Dai, Li, Liu, Long
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 03.09.2021; MDPI
• Subjects: Cement hydration; Chloride; Compressive strength; Concrete; Concrete deterioration; Corrosion products; Corrosion tests; Diffusion rate; Exposure; interfacial transition zone; Mechanical properties; mechanical property; microstructure; pore structure; Rebar; Reinforced concrete; Reinforcing steels; Rivers; Saline soils; Saline solutions; Salt; Salt lakes; Scanning electron microscopy; Soil erosion; Spectrophotometry; Storage modulus; Beijing China; China
• DOI: 10.3390/ma14175054
• ISSN: 1996-1944

The diffusion of sulfate (SO42−) and chloride (Cl−) ions from rivers, salt lakes and saline soil into reinforced concrete is one of the main factors that contributes to the corrosion of steel reinforcing bars, thus reducing their mechanical properties. This work experimentally investigated the corrosion process involving various concentrations of NaCl-Na2SO4 leading to the coupled erosion of concrete. The appearance, weight, and mechanical properties of the concrete were measured throughout the erosion process, and the Cl− and SO42− contents in concrete were determined using Cl− rapid testing and spectrophotometry, respectively. Scanning electron microscopy, energy spectrometry, X-ray diffractometry, and mercury porosimetry were also employed to analyze microstructural changes and complex mineral combinations in these samples. The results showed that with higher Na2SO4 concentration and longer exposure time, the mass, compressive strength, and relative dynamic elastic modulus gradually increased and large pores gradually transitioned to medium and small pores. When the Na2SO4 mass fraction in the salt solution was ≥10 wt%, there was a downward trend in the mechanical properties after exposure for a certain period of time. The Cl− diffusion rate was thus related to Na2SO4 concentration. When the Na2SO4 mass fraction in solution was ≤5 wt% and exposure time short, SO42− and cement hydration/corrosion products hindered Cl− migration. In a concentrated Na2SO4 environment (≥10 wt%), the Cl− diffusion rate was accelerated in the later stages of exposure. These experiments further revealed that the Cl− migration rate was higher than that of SO42−.