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Mechanism of atmospheric corrosion of copper in the presence of submicron ammonium sulfate particles at 300 and 373 K

Journal Article · · Journal of the Electrochemical Society; (United States)
DOI:https://doi.org/10.1149/1.2059261· OSTI ID:6977510
 [1]; ; ;  [2];  [3]
  1. AT and T Bell Labs., Murray Hill, NJ (United States) Max-Planck-Inst. fuer Eisenforschung, Duesseldorf (Germany)
  2. AT and T Bell Labs., Murray Hill, NJ (United States)
  3. Max-Planck-Inst. fuer Eisenforschung, Duesseldorf (Germany)

The corrosion mechanism of copper at 373 and 300 K in the presence of submicron (NH[sub 4])[sub 2]SO[sub 4] particle deposits has been investigated. Several in situ techniques have been used to monitor the corrosion process in real time. At and above the critical relative humidity of (NH[sub 4])[sub 2]SO[sub 4], dissolution of Cu is followed by formation of Cu[sub 2]O, oxidation of Cu(I) ions to Cu(II) ions, and precipitation of antlerite [Cu[sub 3](SO[sub 4])(OH)[sub 4]], brochantite [Cu[sub 4](SO[sub 4])(OH)[sub 6]], or posnjakite [Cu[sub 4](SO[sub 4])(OH)[sub 6][center dot]H[sub 2]O]. The amount of corrosion product formed increases with amount of (NH[sub 4])[sub 2]SO[sub 4] particles, relative humidity (RH), and temperature. The in situ techniques allowed the authors to confirm and refine the individual steps in the multistep mechanism proposed in earlier work.

OSTI ID:
6977510
Journal Information:
Journal of the Electrochemical Society; (United States), Journal Name: Journal of the Electrochemical Society; (United States) Vol. 141:11; ISSN 0013-4651; ISSN JESOAN
Country of Publication:
United States
Language:
English