Comparison of repassivation kinetics of stainless steels in chloride solution

2005 ◽  
Vol 11 (4) ◽  
pp. 309-312 ◽  
Author(s):  
Chan-Jin Park ◽  
Hyuk-Sang Kwon
1994 ◽  
Vol 36 (2) ◽  
pp. 259-268 ◽  
Author(s):  
Canan Kum ◽  
Mahir Alkan ◽  
M. Muhtar Kocakerim

2001 ◽  
Vol 189-191 ◽  
pp. 667-672 ◽  
Author(s):  
A.V.C. Sobral ◽  
Waldyr Ristow ◽  
Olandir Vercino Correa ◽  
César V. Franco ◽  
Isolda Costa

Nukleonika ◽  
2015 ◽  
Vol 60 (4) ◽  
pp. 865-869
Author(s):  
Richard J. Wilbraham ◽  
Colin Boxall

Abstract SO3-Ph-BTBP is a hydrophilic tetra-N-dentate ligand proposed for An(III)/Ln(III) separation by solvent extraction, and a candidate for use in future advanced reprocessing schemes such as GANEX and SANEX. We present the first study of the effect of SO3-Ph-BTBP on the corrosion behavior of stainless steels. Specifically, studies have been performed using steels and conditions equivalent to those found in relevant nuclear reprocessing flow sheets. SO3-Ph-BTBP has been shown to have little effect on either steel passivation or reductive dissolution. However, if driven cathodically into a region of hydrogen evolution at the electrode surface or conversely anodically into a region of transpassive dissolution, observed currents are reduced in the presence of SO3-Ph-BTBP, suggesting corrosion inhibition of the steel potentially through weak absorption of a SO3-Ph-BTBP layer at the metal-solution interface. The lack of any observed corrosion acceleration via complexation of Fe3+ is surprising and has been suggested to be due to the slow extraction kinetics of SO3-Ph-BTBP as a result of a requirement for a trans- to cis-conformational change before binding.


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