Abstract
Electrochemical cells with a rotating disc electrode are the preferred devices to characterize electrochemical reactions because simple analytical expressions can be used to interpret the information obtained from physical experiments. These equations assume that the velocity field in the vicinity of the electrode active face is in accordance with the ideal behavior described by von Kármán. Experimental liquid velocity measurements inside the cell reported in recent works suggest that the actual liquid flow pattern is not fully in accordance with the assumed ideal behavior. In this work, the Computational Fluid Dynamics technique was employed to characterize numerically the flow pattern inside the electrochemical cell. By using a three-dimensional model, symmetric conditions were not imposed. A biphasic system was employed to evaluate the influence of liquid free surface over the flow pattern. Unsteady state numerical simulations were performed using the commercial software Fluent. Multiple electrode rotation speeds and several cell sizes were employed. Contrary to the assumed behavior, it was obtained that the flow pattern inside the electrochemical cell is not symmetric due to the synergetic effect of the cell walls, the submerged electrode side wall and the liquid free surface. This work states that the differences between actual and the ideal flow patterns can be minimized with plain electrode and cell geometrical modifications.
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