J. Flis et E. Sikora, IMPEDANCE AND TRANSIENT STUDY OF IRON AND IRON PHOSPHORUS ALLOY IN CARBONATE BICARBONATE SOLUTION WITH PHOSPHATE ANIONS, Electrochimica acta, 39(8-9), 1994, pp. 1145-1149
Anodic oxidation of iron and Fe-1.82% P was studied at 75-degrees-C in
0.5 M Na2CO3 + 1.0 M NaHCO3 with the addition of 0.5 M and 2.0 M Na2H
PO4. Polarization curves and potentiostatic transients showed that ano
dic currents for the Fe-P alloy were higher than for iron. The charge
of the active dissolution preceding the onset of passivation was, for
the Fe-P alloy, about four times bigger than for iron, whereas current
decays following the start of the passivation were slower. Addition o
f 2.0 M Na2HPO4 resulted in an anodic activation of iron similar to th
at caused by phosphorus, demonstrated by higher current of polarizatio
n curves, higher initial currents at potentials of the passive region,
slower current decays and higher interfacial capacitance C(if) in the
active-passive transition region. High C(if), reaching 60 F m-2 at th
e potential of -0.65 V (sce), can be ascribed to redox reactions invol
ving ferrous phosphate and Fe(III) species. It is suggested that the e
ffect of phosphorus on the anodic behavior of iron is associated mainl
y with the formation of phosphates as a result of oxidation of phospho
rus on the metal surface.