TY - JOUR
T1 - Kinetics and mechanism of the electrochemical formation of iron oxidation products on steel immersed in sour acid media
AU - Hernández-Espejel, Antonio
AU - Palomar-Pardavé, Manuel
AU - Cabrera-Sierra, Román
AU - Romero-Romo, Mario
AU - Ramírez-Silva, María Teresa
AU - Arce-Estrada, Elsa M.
PY - 2011/3/3
Y1 - 2011/3/3
N2 - From electrochemical techniques (cyclic voltammetry, potential steps, and EIS), XRD, and SEM-EDX, the kinetics and mechanism of anodic film formation applying anodic potential steps on steel immersed in sour acid media was determined. It was found, from a thermodynamic analysis, based on equilibrium phase diagrams of the system considered in this work, that iron oxidation may produce different new solid phases, depending on the applied potential, the first being the iron oxidation associated with formation of FeS(c) species, which in turn can be reoxidized to FeS2(c) or even to Fe2O3(c) at higher potential values. From analysis of the corresponding experimental potentiostatic current density transients, it was concluded that the electrochemical anodic film formation involves an E 1CE2 mechanism, whereby the first of the two simultaneous processes were the Fe electrochemical oxidation (E1) followed by FeS precipitation (C) that occurs by 3D nucleation and growth limited by mass transfer reaction and FeS oxidation (E2) forming a mix of different stoichiometry iron sulphides and oxides. From EIS measurements, it was revealed that the anodic film's charge transfer resistance diminishes as the potential applied for its formation becomes more anodic, thus behaving poorly against corrosion.
AB - From electrochemical techniques (cyclic voltammetry, potential steps, and EIS), XRD, and SEM-EDX, the kinetics and mechanism of anodic film formation applying anodic potential steps on steel immersed in sour acid media was determined. It was found, from a thermodynamic analysis, based on equilibrium phase diagrams of the system considered in this work, that iron oxidation may produce different new solid phases, depending on the applied potential, the first being the iron oxidation associated with formation of FeS(c) species, which in turn can be reoxidized to FeS2(c) or even to Fe2O3(c) at higher potential values. From analysis of the corresponding experimental potentiostatic current density transients, it was concluded that the electrochemical anodic film formation involves an E 1CE2 mechanism, whereby the first of the two simultaneous processes were the Fe electrochemical oxidation (E1) followed by FeS precipitation (C) that occurs by 3D nucleation and growth limited by mass transfer reaction and FeS oxidation (E2) forming a mix of different stoichiometry iron sulphides and oxides. From EIS measurements, it was revealed that the anodic film's charge transfer resistance diminishes as the potential applied for its formation becomes more anodic, thus behaving poorly against corrosion.
UR - http://www.scopus.com/inward/record.url?scp=79951973540&partnerID=8YFLogxK
U2 - 10.1021/jp106851b
DO - 10.1021/jp106851b
M3 - Artículo
C2 - 21302956
SN - 1520-6106
VL - 115
SP - 1833
EP - 1841
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 8
ER -