Investigation of Iron Dissolution Mechanism in Acidic Solutions with and without Dissolved CO2—Part II: Time of Flight-Secondary Ion Mass Spectrometry 3D Mapping

Author:

Wang Luntao123ORCID,Wang Huiru143ORCID,Moradighadi Negar1ORCID,Seyeux Antoine2,Pailleret Alain4,Nešić Srdjan1ORCID,Marcus Philippe2

Affiliation:

1. *Institute for Corrosion Multiphase Technology, Ohio University, Athens Ohio 45701.

2. **Université PSL, CNRS—Chimie ParisTech, Institut de Recherche de ChimieParis, Groupe Physico-Chimie des Surfaces, 75005 Paris, France.

3. ****These authors equally contributed to this work.

4. ***Sorbonne Université, CNRS, Laboratoire Interfaces et Systèmes Electrochimiques, 75005, Paris, France.

Abstract

Time-of-flight-secondary ion mass spectrometry (ToF-SIMS) 3D mapping and depth profiling were used to study the anodic iron dissolution mechanisms of mild steel in chloride-containing aqueous CO2 environments. The technique detected adsorbed hydroxide and chloride intermediates formed during the corrosion process, consistent with the proposed multipath reaction mechanism for anodic iron dissolution reaction. Despite the presence of aqueous carbonic species and their observed effect on the kinetics of iron dissolution, no additional adsorbed intermediates have been detected in aqueous CO2 environments, indicating that carbonic species do not directly participate in the iron dissolution reaction. ToF-SIMS 3D mapping results on characterization of the specimens immersed in a chloride-containing solution with and without CO2 suggest that one role of aqueous carbonic species CO2 could be to accelerate the adsorption of chloride ions and the formation of chloride intermediates.

Publisher

Association for Materials Protection and Performance (AMPP)

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