Mechanisms of copper corrosion and electrodissolution in naturally aerated, stagnant 0.5 M H(2)SO(4) were investigated by means of electrochemical techniques, compared with deaerated measurements. The role of dissolved oxygen was suggested, and three models were proposed in -0.05 similar to 0.15 V vs. SCE range. Near to corrosion potential, chemical redox between cuprous intermediate and oxygen reduction reaction (ORR) intermediate accelerated copper corrosion, and corrosion rate was controlled by a combined cathodic kinetic-anodic diffusion process. in low and high potential ranges, chemical redox, occurred between cuprous intermediate and oxygen molecule, synergistically accelerated the electrodissolution of copper. (C) 2009 Elsevier Ltd. All rights reserved.
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