Phosphate- or chromate-based
industrially produced conversion layers,
while effectively increasing adhesion for organic coatings and corrosion
resistance, come at the cost of environmentally problematic and harmful
treatment solutions and waste. In this respect, layered double hydroxide
(LDH)-based conversion layers offer an environmentally benign alternative
without toxicologically concerning compounds in the treatment solution.
Here, we study an LDH conversion layer on Zn–Al–Mg-coated
steel (ZM-coated steel), which was produced by immersion into a carbonate-
and magnesium-containing alkaline solution. The mechanism and kinetics
of the conversion layer formation were investigated with in situ open
circuit potential measurements, cyclic voltammetry (CV), and scanning
electron microscopy (SEM). Acceleration of the LDH layer formation
through high convection in the treatment solution was found. This
was attributed to a higher oxygen availability at the metal/solution
interface because no diffusion-limited state during the layer formation
is reached due to high convection. The importance of oxygen within
the kinetics indicates a corrosion-like mechanism, with cathodic and
anodic sites on the steel sample. The LDH formation happens by co-precipitation
of ions present in the treatment solution and dissolved ions from
the ZM-coated steel. With CV, SEM, and X-ray diffraction, the growth
of the LDH conversion layer was investigated with respect to the immersion
time. It was found that after 30 s, the sample surface was almost
fully covered with an LDH layer, and with the increasing immersion
time, the layer grows in thickness. Increased understanding on the
kinetics and mechanism of the LDH conversion layer formation on ZM-coated
steel gives rise to a targeted optimization of the treatment solution
and process parameters.