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Effect of [HCO{sub 3}{sup {minus}}+CO{sub 3}{sup 2{minus}}] on corrosion crevice repassivation potential of carbon steel in simulated bentonite environment

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OSTI ID:264465
;  [1]
  1. Ishikawajima-Harima Heavy Industries Co., Ltd., Tokyo (Japan). Research Inst.
In order to evaluate the localized corrosion susceptibility of carbon steel in water containing bentonite, the critical pH for depassivation, pH{sub d}, the critical potential for crevice corrosion, E{sub R,CREV}, and the free corrosion potential, Esp, were determined in simulated aqueous solutions of 1 to 100 mmol/L [bicarbonate-carbonate], 1 to 1,000 mmol/L [NaCl], and pH of 7 to 12. The following results were obtained: (1) E{sub R,CREV} increases with increasing [bicarbonate-carbonate] concentration. The relationship can be described as a function of the ratio of [Cl{sup {minus}}/bicarbonate-carbonate], (2) the Esp increases with increasing pH in the passive region, and (3) the pH{sub d} shows [bicarbonate-carbonate] concentration dependency. This paper also discusses the relationship between critical initiation potential for device corrosion of carbon steel, [Cl{sup {minus}}], and [bicarbonate-carbonate] anion. The crevice corrosion that occurs on passivated metals and alloys is characterized by determinable critical initiation potential that can be induced in a potential range nobler than its critical potential.
OSTI ID:
264465
Report Number(s):
CONF-951155--; ISBN 1-55899-315-0
Country of Publication:
United States
Language:
English