Electrochemical behaviour and surface conductivity of niobium carbide-modified austenitic stainless steel bipolar plate

2014 ◽  
Vol 246 ◽  
pp. 775-782 ◽  
Author(s):  
Lixia Wang ◽  
Juncai Sun ◽  
Bin Kang ◽  
Song Li ◽  
Shijun Ji ◽  
...  
Author(s):  
Heli Wang ◽  
Glenn Teeter ◽  
John A. Turner

Austenitic 349 stainless steel was nitrided in an NH3 plasma. A low interfacial contact resistance was obtained with the nitrided steel. Glancing angle X-ray diffraction suggests that the nitrided layer is very thin and possibly amorphous. X-ray photoelectron spectroscopy (XPS) studies show that the nitrided layer is composed of mixed oxides and nitrides of Fe3+ and Cr3+. Contaminations of V and Sn were also observed, though their influence on the as-nitrided surface conductivity is not clear. The nitrided samples were investigated in a simulated polymer electrolyte membrane fuel cell (PEMFC) environment, and showed excellent corrosion resistance. The XPS depth profile indicated that the passive film, which formed on the plasma-nitrided steel in the PEMFC anode environment, is composed of mixed oxides and nitrides, in which chromium oxide/nitride dominates the surface chemistry. No V or Sn was detected on the surface after the polarization tests. For the PEMFC bipolar plate application, nitridation in NH3 plasma is a promising surface treatment approach, though more research is needed to investigate the influence of the plasma density and substrate bias on the surface conductivity and performance of the nitrided steel in PEMFC environments.


2020 ◽  
Vol 7 (10) ◽  
pp. 105402
Author(s):  
Ely Wagner Ferreira Sabará ◽  
Valter Pereira ◽  
André Luiz Molisani ◽  
Lecino Caldeira ◽  
Rhuan Costa Souza ◽  
...  

CORROSION ◽  
10.5006/3725 ◽  
2021 ◽  
Author(s):  
Ronald Clark ◽  
Choen Chan ◽  
W. Walters ◽  
Dirk Engelberg ◽  
Geraint Williams

Advanced gas-cooled reactor (AGR) oxide fuels used in the UK are clad in bespoke grade 20%Cr-25%Ni-Nb austenitic stainless steel. Electrochemistry was first applied to correlate the breakdown potential with chloride ion concentration, temperature and pH for this alloy. At near-neutral pH the unsensitized material exhibited a linear E<sub>b</sub> = A + B log10[Cl<sup>-</sup>] relationship, where A = 0.7 V (vs. SCE), and B = 0.098 V/decade. Scanning Kelvin probe force microscopy revealed grain boundary regions in the heat-treated material up to 65 mV less noble to the matrix, whereas un-dissolved niobium carbide (NbC) precipitates were up to 55 mV more noble to the matrix. In-situ time-lapse microscopy and post-corrosion observations confirmed that sensitized grain boundaries were susceptible to pitting corrosion, further developing along intergranular corrosion pathways. It has however been shown that micro galvanic coupling between the Nb precipitates and matrix and / or sensitized grain boundary regions is not a factor in corrosion initiation as all experiments were performed under external potential control. Post corrosion observations showed the presence of pits at NbC precipitates promoting grain boundary corrosion. It is postulated that corrosion initiates at NbC precipitates as a pit, and when in close vicinity to Cr-depleted grain boundaries, then propagates along grain boundaries as intergranular corrosion.


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