Information obtained from two amperometric sensors and from a potentiometric sensor for monitoring hydrogen (H) in steel in contact with corrosive solutions saturated with hydrogen sulfide (H2S) at ambient temperature was compared. The apparent diffusion coefficient (Dapp) for H in the steel as determined by experiments using the amperometric sensors was shown to be independent of H concentration in the steel (cH). Experiments with the potentiometric sensor indicated Dapp values increased with increasing cH. The calculated H concentration at the surface of the steel in contact with the corrosive medium (chi), as obtained from the two amperometric sensors, showed poor agreement. The equivalent pressure of H in the steel (pH2eq), as calculated from the voltage measurement of the potentiometric sensor, was strongly dependent on pH of the corrosive solution.

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