Journal
CORROSION SCIENCE
Volume 44, Issue 11, Pages 2507-2528Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0010-938X(02)00021-5
Keywords
copper; corrosion; monochloramine; electrochemical impedance spectroscopy (EIS); polarization resistance (R-p)
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The corrosion of pure copper for a period of 2-30 days was investigated in simulated tap water containing monochloramine (normally at 4.0 mg/l) in the pH range of 7.6-8.4, using electrochemical impedance spectroscopy, potentiodynamic scan, X-ray photoelectron spectroscopy (XPS), inductively coupled plasma and scanning electronic microscopy (SEM). The XPS spectra and SEM indicated that after 8 days of immersion, the copper surface was covered by both cupric and cuprous oxides. Diffusion in the oxide film was found having a significant effect on the corrosion process. The results showed that at pH 8.0 the polarization resistance (R-P) increased with time during the first 6 days and reached relative stability after 8 days. An equivalent circuit model was proposed to fit the corrosion process, and the elements extracted from the model predicted a corrosion rate in the order of 0.1 mum/yr at pH of 8.0. The values of R-P increased with higher pH for all 2, 4, 6, and 8-day immersions, but decreased at a higher monochloramine concentration of 20 mg/l. In the control experiment, R-P had the largest value after a 30-day immersion time. Dissolved inorganic carbon (DIC) enhancess the dissolution of copper by a factor of 2, when the concentration of DIC increased from 0.59 to 4.0 mM. Increasing ionic strength from 0.005 to 0.02 M reduced R-P, but the increase of R-P with immersion time was faster at higher ionic strengths. (C) 2002 Elsevier Science Ltd. All rights reserved.
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