2019
DOI: 10.1016/j.corsci.2019.108198
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Reduction of austenite-ferrite galvanic activity in the heat-affected zone of a Gleeble-simulated grade 2205 duplex stainless steel weld

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Cited by 43 publications
(17 citation statements)
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“…The environment containing 2 mol L -1 H 2 SO 4 + 0.5 mol L -1 HCl in Figure 9 enhanced the anodic current density in the active-to-passive transition region, and it is important to point out that two distinguishable peaks were observed in this region, consistent with those reported by other authors 29,35 . According to the literature 27 , preferential dissolution of ferrite phase occurred at lower peak potential (≈ -270 mV to the base metal), while the austenite phase corroded at a fast rate at higher peak potential (≈ -220 mV to the base metal).…”
Section: Ferrite/austenite -Electrochemical Activitysupporting
confidence: 89%
See 1 more Smart Citation
“…The environment containing 2 mol L -1 H 2 SO 4 + 0.5 mol L -1 HCl in Figure 9 enhanced the anodic current density in the active-to-passive transition region, and it is important to point out that two distinguishable peaks were observed in this region, consistent with those reported by other authors 29,35 . According to the literature 27 , preferential dissolution of ferrite phase occurred at lower peak potential (≈ -270 mV to the base metal), while the austenite phase corroded at a fast rate at higher peak potential (≈ -220 mV to the base metal).…”
Section: Ferrite/austenite -Electrochemical Activitysupporting
confidence: 89%
“…This would certainly mean that ferrite stabilising elements are partly re-distributed into the austenite, which in turn would also affect the corrosion resistance and associated Volta potential differences. 29 4. Posttest SEM investigation indicated that the reactivation peaks of the DL-EPR test can be attributed to the preferential corrosion attack of Cr-depleted regions around Cr-carbides and Cr-nitrides.…”
Section: Skpfm Assessmentmentioning
confidence: 99%
“…In contrast, by keeping the environment constant, the overall shape of the active-passive transition peak as well as the magnitude is then a function of the chemical composition and alloying elements. The latter is easily demonstrated with duplex stainless steel microstructures, which show a convoluted active-passive transition peak during electrochemical polarisation, representing overlapping chromium-rich ferrite and nickel-rich austenite peaks [27][28][29].…”
Section: Resultsmentioning
confidence: 92%
“…Electrochemical tests are well established techniques employed in studies of corrosion and passivation of stainless steels [2][3][4][5][6][7] . The use of a micrometric exposed surface area enables more precise evaluation of the electrochemical behavior of stainless steel surfaces [8][9][10][11][12][13] .…”
Section: Introductionmentioning
confidence: 99%