Effects of Zn and Ni addition on the Co incorporation in 316 SS oxide formed under simulated BWR conditions

Advanced microstructural and microchemical analyses provided critical insights into the mechanism of Co incorporation into the oxide formed on 316 Stainless Steel (SS), when exposed to simulated Boiling Water Reactor (BWR) conditions. The study showed that the presence of Zn and/or Ni injected into the water significantly influenced Co incorporation. Coupons of 316 SS were exposed to multistage oxidation tests under low-level Hydrogen Water Chemistry (HWC) (H:O molar ratio ∼8) at 288°C, both in the absence and the presence of metal cations injection (Zn, Ni, Co). Moreover, Online NobleChem™ (OLNC) was applied in an intermediate exposure stage on pre-oxidised coupons to show how the transition from a non-catalytic to a catalytic oxide surface impacts the oxide properties. The application of OLNC did not substantially influence the incorporation of metal cations in the oxide. Notably, the study showed that Co was preferentially incorporated into the normal spinel oxides, thus suggesting that Co 2+ prefers the tetrahedral sites of these spinel, similar to Zn 2+ . This translated into a Co uptake mitigation effect when 10 ppb of Zn was injected. Conversely, in the presence of 10 ppb of Ni in the water, Co uptake was not mitigated, suggesting that Ni 2+ does not compete with Co 2+ for the same interstitial sites of the spinel oxides. However, a mitigation effect on Co uptake was observed when Zn and Ni were injected simultaneously, indicating a synergistic effect of these metal cations on the Co incorporation mechanism. 316 SS coupons were exposed to BWR water chemistry with/without Zn, Ni and Co cations OLNC transitioned the oxide surface to catalytic without altering cation incorporation Zn 2+ high preference for the tetrahedral sites of normal spinel mitigated Co uptake Ni 2+ did not lessen Co 2+ uptake, indicating different interstitial site preference Zn and Ni cooperation mitigated even more Co incorporation in the oxide

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Journal
Corrosion Science
Published
2025-05-09
DOI
https://doi.org/10.1016/j.corsci.2025.113023
Primary Topic
Nuclear Materials and Properties
Type
article
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article

Effects of Zn and Ni addition on the Co incorporation in 316 SS oxide formed under simulated BWR conditions

Hideyuki Hosokawa, Yoichi Wada, Tsuyoshi Ito, M.G. Burke et al.
Corrosion Science
Nuclear Materials and Properties
article

Effects of Zn and Ni addition on the Co incorporation in 316 SS oxide formed under simulated BWR conditions

Hideyuki Hosokawa, Yoichi Wada, Tsuyoshi Ito, M.G. Burke, Jonathan Duff, Fabio Scenini, D. W. Capone, Makoto Nagase
article en

Abstract

Advanced microstructural and microchemical analyses provided critical insights into the mechanism of Co incorporation into the oxide formed on 316 Stainless Steel (SS), when exposed to simulated Boiling Water Reactor (BWR) conditions. The study showed that the presence of Zn and/or Ni injected into the water significantly influenced Co incorporation. Coupons of 316 SS were exposed to multistage oxidation tests under low-level Hydrogen Water Chemistry (HWC) (H:O molar ratio ∼8) at 288°C, both in the absence and the presence of metal cations injection (Zn, Ni, Co). Moreover, Online NobleChem™ (OLNC) was applied in an intermediate exposure stage on pre-oxidised coupons to show how the transition from a non-catalytic to a catalytic oxide surface impacts the oxide properties. The application of OLNC did not substantially influence the incorporation of metal cations in the oxide. Notably, the study showed that Co was preferentially incorporated into the normal spinel oxides, thus suggesting that Co 2+ prefers the tetrahedral sites of these spinel, similar to Zn 2+ . This translated into a Co uptake mitigation effect when 10 ppb of Zn was injected. Conversely, in the presence of 10 ppb of Ni in the water, Co uptake was not mitigated, suggesting that Ni 2+ does not compete with Co 2+ for the same interstitial sites of the spinel oxides. However, a mitigation effect on Co uptake was observed when Zn and Ni were injected simultaneously, indicating a synergistic effect of these metal cations on the Co incorporation mechanism. 316 SS coupons were exposed to BWR water chemistry with/without Zn, Ni and Co cations OLNC transitioned the oxide surface to catalytic without altering cation incorporation Zn 2+ high preference for the tetrahedral sites of normal spinel mitigated Co uptake Ni 2+ did not lessen Co 2+ uptake, indicating different interstitial site preference Zn and Ni cooperation mitigated even more Co incorporation in the oxide

Corrosion ScienceVol. 253
Idaho National Laboratory (US), Paul Scherrer Institute (CH), University of Manchester (GB), Henry Royce Institute (GB), Hitachi (Japan) (JP)
Openalex Percentile: Top 93%
Nuclear Materials and Properties
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