Abstract
Flow accelerated corrosion (FAC) is divided into two processes: a corrosion (chemical) process and a flow dynamics (physical) process. The former is the essential process to cause FAC and the latter is the accelerating process to enhance FAC occurrence. The chemical process in the surface boundary layer is analyzed to evaluate FAC rate. Contributions of flow dynamics on wall thinning rate due to FAC are expressed as a function of mass transfer coefficient but not that of flow velocity. FAC evaluation procedures were divided into 5 steps as follows. (1) Flow pattern and temperature in each elemental volume along the flow path were obtained with 1D computational flow dynamics (CFD) codes, (2) corrosive conditions, e.g., oxygen concentration and electrochemical corrosion potential (ECP) along the flow path were calculated with a hydrazine oxygen reaction code, (3) precise flow patterns and mass transfer coefficients at the structure surface were calculated with 3D CFD codes, (4) danger zones were evaluated by coupling major FAC parameters, and then, (5) wall thinning rates were calculated with the coupled model of static electrochemical analysis and dynamic double oxide layer analysis at the identified danger zone. Anodic and cathodic current densities and ECPs were calculated with the static electrochemistry model and ferrous ion release rate determined by the anodic current density was used as input for the dynamic double oxide layer model. Thickness of the oxide film and its characteristics determined by the dynamic double oxide layer model were used for the electrochemistry model to determine the resistances of cathodic current from the bulk to the surface and anodic current from the surface to the bulk. Two models were coupled to determine local corrosion rate and ECP for various corrosive conditions. The calculated results of the coupled models had good agreement with the measured ones.
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