Considerations for realistic atmospheric environments: An application to corrosion testing

Measured salt compositions in dust collected over roughly the last decade from surfaces of in-service stainless-steel alloys at four locations around the United States are presented, along with the predicted brine compositions that would result from deliquescence of these salts. The salt composition...

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Veröffentlicht in:The Science of the total environment 2023-08, Vol.885, p.163751-163751, Article 163751
Hauptverfasser: Katona, R.M., Knight, A.W., Maguire, M., Bryan, C.R., Schaller, R.F.
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Sprache:eng
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Zusammenfassung:Measured salt compositions in dust collected over roughly the last decade from surfaces of in-service stainless-steel alloys at four locations around the United States are presented, along with the predicted brine compositions that would result from deliquescence of these salts. The salt compositions vary greatly from ASTM seawater and from laboratory salts (i.e., NaCl or MgCl2) commonly used on corrosion testing. The salts contained relatively high amounts of sulfates and nitrates, evolved to basic pH values, and exhibited deliquescence relative humidity values (RH) higher than seawater. Additionally, inert dust in components were quantified and considerations for laboratory testing are presented. The observed dust compositions are discussed in terms of the potential corrosion behavior and are compared to commonly used accelerated testing protocols. Finally, ambient weather conditions and their influence on diurnal fluctuations in temperature (T) and RH on heated metal surfaces are evaluated and a relevant diurnal cycle for laboratory testing a heated surface has been developed. Suggestions for future accelerated tests are proposed that include exploration of the effects of inert dust particles on atmospheric corrosion, chemistry considerations, and realistic diurnal fluctuations in T and RH. Understanding mechanisms in both realistic and accelerated environments will allow development of a corrosion factor (i.e., scaling factor) for the extrapolation of laboratory-scale test results to real world applications. [Display omitted] •Chemical analysis of salt distributions at four locations in the United States•Thermodynamic modeling of salt evolution as a function of relative humidity•Measured salt compositions vary greatly from ASTM seawater and from laboratory salts•Inert dust components quantified and could accelerate corrosion reactions•Development of realistic diurnal fluctuations on a heated metal surface for laboratory testing
ISSN:0048-9697
1879-1026
DOI:10.1016/j.scitotenv.2023.163751