Abstract
Chloride ions (Cl−)-induced corrosion is one of the main degradation mechanisms in reinforced concrete (RC) structures. In most situations, the degradation initiates with the transport of Cl− from the surface of the concrete towards the reinforcing steel. The accumulation of Cl− at the steel-concrete interface could initiate reinforcement corrosion once a threshold Cl− concentration is achieved. An accurate numerical model of the Cl− transport in concrete is required to predict the corrosion initiation in RC structures. However, existing numerical models lack a representation of the heterogenous concrete microstructure resulting from the varying environmental conditions and the indirect effect of time dependent temperature and relative humidity (RH) on the water adsorption and Cl− binding isotherms. In this study, a numerical model is developed to study the coupled transport of Cl− with heat, RH and oxygen (O2) into the concrete. The modeling of the concrete microstructure is performed using the Virtual Cement and Concrete Testing Laboratory (VCCTL) code developed by the U.S. National Institute of Standards and Technology (NIST). The concept of equivalent maturation time is utilized to eliminate the limitation of simulating concrete microstructure using VCCTL in specific environmental conditions such as adiabatic. Thus, a time-dependent concrete microstructure, which depends on the hydration reactions coupled with the temperature and RH of the environment, is achieved to study the Cl− transport. Additionally, Cl− binding isotherms, which are a function of the pH of the concrete pore solution, Cl− concentration, and weight fraction of mono-sulfate aluminate (AFm) and calcium-silicate-hydrate (C-S-H), obtained from an experimental study by the same authors are utilized to account for the Cl− binding of cement hydration products. The temperature dependent RH diffusion was considered to account for the transport of Cl− with moisture transport. The temperature and RH diffusion in the concrete domain, composite theory, and Cl− binding and water adsorption isotherms are used in combination, to estimate the ensuing Cl− diffusion field within the concrete. The coupled transport process of heat, RH, Cl−, and O2 is implemented in the Multiphysics Object-Oriented Simulation Environment (MOOSE) developed by the U.S. Idaho National Laboratory (INL). The model was verified and validated using data from multiple experimental studies with different concrete mixture proportions, curing durations, and environmental conditions. Additionally, a sensitivity analysis was performed to identify that the water-to-cement (w/c) ratio, the exposure duration, the boundary conditions: temperature, RH, surface Cl− concentration, Cl− diffusion coefficient in the capillary water, and the critical RH are the important parameters that govern the Cl− transport in RC structures. In a case study, the capabilities of the developed numerical model are demonstrated by studying the complex 2D diffusion of Cl− in a RC beam located in two different climatic regions: warm and humid weather in Galveston, Texas, and cold and dry weather in North Minnesota, Minnesota, subjected to time varying temperature, RH, and surface Cl− concentrations.
Highlights
The transport of chloride ions (Cl− ) from the concrete surface is the most influential aspect of corrosion-induced deterioration in reinforced concrete (RC) structures
Since the chloride-induced degradation starts with the corrosion reactions at the steelconcrete interface, O2 transport is included in the modeling of the coupled transport of heat, relative humidity (RH), and Cl−
The concrete mixture details along with the modeling parameters are given in Table 5 for completeness
Summary
The transport of chloride ions (Cl− ) from the concrete surface is the most influential aspect of corrosion-induced deterioration in reinforced concrete (RC) structures. Airborne Cl− or Cl− from seawater is carried into concrete over time and this process is usually exacerbated by the wetting and drying cycles. In cold regions, the concrete surface is subjected to deicing salts that penetrate into the concrete through various mechanisms including sorption and diffusion. Cl− may be present in the concrete pore structure when Cl− bearing salts (such as calcium chloride: CaCl2 ) are used in the fresh concrete to accelerate the hydration process and achieve a higher early strength. The presence of Cl− beyond a threshold value at the steel-concrete interface starts the corrosion-induced degradation process. A study of the transport of Cl− is essential to estimate the time for corrosion initiation as well as for corrosion propagation in service life estimation of RC structures
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