The inhibition effect and mechanism of l-cysteine on the corrosion of bronze covered with a CuCl patina

Artificial patina formation onto copper-based alloys: Chloride and sulphate induced corrosion processes

This review on copper runoff dispersed from unsheltered naturally patinated copper used for roofing and facades summarizes and discusses influencing factors, available literature, and predictive models, and the importance of fate and speciation for environmental risk assessment. Copper runoff from outdoor surfaces is predominantly governed by electrochemical and chemical reactions and is highly dependent on given exposure conditions (size, inclination, geometry, degree of sheltering, and orientation), surface parameters (age, patina composition, and thickness), and site-specific environmental conditions (gaseous pollutants, chlorides, rainfall characteristics (amount, intensity, pH), wind direction, temperature, time of wetness, season). The corrosion rate cannot be used to assess the runoff rate. The extent of released copper varies largely between different rain events and is related to dry and wet periods, dry deposition prior to the rain event and prevailing rain and patina characteristics. Interpreta...

Critical review: Copper runoff from outdoor copper surfaces at atmospheric conditions.

The atmospheric corrosion of copper in pure coastal atmospheres has not been extensively studied. This paper presents the results of research carried out in pure coastal atmospheres with annual chloride deposition rates of between 110–1640 mg/m2·d. Copper specimens (99.99 wt % Cu) were exposed for 3, 6, 9, and 12 months at six testing stations located at different distances from the seashore. Tests were performed to determine the copper corrosion rate, the surface area coated with corrosion products, and the evolution of both magnitudes with exposure time. Conventional and grazing X-ray diffraction techniques were used to analyze the corrosion products formed—cuprite and the polymorphs botallackite, atacamite, and clinoatacamite—and their presence through the patina thickness, while scanning electron microscopy/energy dispersive X-ray spectrometry was employed to study the morphology of the resulting corrosion layers. The most relevant findings are a notable increase in atacamite and clinoatacamite formation at higher atmospheric salinity levels and longer exposure times, and the flaking-off of the corrosion product layer formed in the marine atmospheres with the highest chloride deposition rates.

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Corrosion of Copper in Unpolluted Chloride-Rich Atmospheres

The marine environmental condition, especially NaCl, has been identified as one of the major sources of contamination on the performance of open cathode Proton Exchange Membrane Fuel Cells (PEMFC) system, when the power source is based on fuel cells for marine applications like submarines, navy ships etc., In the present paper, we have studied the performance of PEMFCs under the marine environment for a longer duration and also the recovery mechanism of the PEMFC power pack after contamination. It has been observed that the NaCl is a major contaminant for PEMFC, compared to NO
 x
 and SO
 x
 , which are major contaminants for fuel cells operating in the land regions. We have observed a performance loss of 60 % in PEMFC, when operated for 48 h, due to poisoning of PEMFC by NaCl vapours. The recovery of the stack is attempted by repeated water washing on the cathode side of the fuel cell, presuming that the salts get deposited only on the surface of the electrodes and the performance is easily recoverable. The recovery mechanisms are analysed by constant-current discharging operation and by modified experimental methods and are reported here. The performance vagaries in fuel cells due to sea water contamination is also analysed by linear fit and it is found that the rate of power increment after water wash is higher than the rate of power increment, around 11.5 W/10 h compared to normal environmental conditions, which is 4.1 W/10 h.

W. Farro

Papers

Influence of seawater and its aerosols on copper patina composition