Atmospheric Corrosion of Copper in the Presence of Acid Ammonium Sulfate Particles
| Autor: | R. E. Lobnig, C. A. Jankoski |
|---|---|
| Rok vydání: | 1998 |
| Předmět: |
Kelvin probe force microscope
Cuprite Ammonium sulfate Renewable Energy Sustainability and the Environment Inorganic chemistry chemistry.chemical_element Electrolyte Condensed Matter Physics Microstructure Copper Surfaces Coatings and Films Electronic Optical and Magnetic Materials Corrosion chemistry.chemical_compound chemistry visual_art Materials Chemistry Electrochemistry visual_art.visual_art_medium Ammonium |
| Zdroj: | Journal of The Electrochemical Society. 145:946-956 |
| ISSN: | 1945-7111 0013-4651 |
| DOI: | 10.1149/1.1838371 |
| Popis: | Basic copper sulfates, CU x SO 4 (OH) y , and cuprite, CU 2 O, are the major corrosion products found during field exposure of copper. The active species of the atmosphere which lead to formation of these corrosion products are, however, still uncertain. In this study, we investigated whether submicron acid ammonium sulfate particles, NH 4 HSO 4 , can lead to formation of a patina with the above composition. The corrosion process was followed by various analytical techniques, including in situ analysis by X-ray diffraction, pH, and scanning Kelvin probe measurements. The main corrosion products found at 300 K are mixed ammonium copper sulfates, (NH 4 ) 2 Cu(SO 4 )(OH) 2 .xH 2 O, and small amounts of cuprite, CU 2 O. Those formed at 373 K are antlerite, Cu 3 (SO 4 )(OH) 4 , and cuprite CU 2 O. From the room temperature results, NH 4 HSO 4 does not appear to be responsible for patina formation. The corrosion mechanism is discussed and compared to that of copper with (NH 4 ) 2 SO 4 particles, which has earlier been shown. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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