L. Sziraki et al., Zn and Zn-Sn alloy coatings with and without chromate layers. Part I: Corrosion resistance and structural analysis, J APPL ELEC, 29(8), 1999, pp. 927-937
The aqueous corrosion resistances of Zn and Zn-Sn (similar to 20 wt% Sn) el
ectrodeposits, passivated by immersion in chromating solution with differen
t ratios of Cr(VI) to activating ions, are compared. The electrochemical be
haviour of various chromated and nonchromated coatings were investigated in
deaerated 0.5 mol dm(-3) Na2SO4/pH 5 solution using a.c. impedance and d.c
. polarization techniques. The polarization curves revealed that the chroma
te layers influence both the cathodic and anodic reactions. The corrosion r
ate of each specimen decreases with time due to the accumulation of corrosi
on products. The dark yellow (DY) chromate film on the Zn-Sn alloy and the
iridiscent yellow (IY) on Zn yields the best protective ability in agreemen
t with the assessment of prolonged salt spray chamber tests. These chromate
layers resembling cracked mud become permeable to the electrolyte after im
mersion and, as a consequence of the transformation and the leaching of cer
tain Cr compounds, a very porous agglomerate of corrosion products forms. T
he morphology and structure of dark yellow chromated Zn-Sn alloy was also i
nvestigated by transmission electromicroscopy (TEM) and scanning electronmi
croscopy with microprobe (SEM/EDS) analyses before and after corrosion. The
depth profile of the corroded surface chemical composition was determined
by X-ray photoelectron spectroscopy (XPS).