Abstract
This paper studies the effect of water as an oxidation agent and also of oxygen on zinc corrosion kinetics in active state in concrete, using high-sensitivity electrical resistance sensors. It was proven that zinc corrosion in active state is strongly affected by the presence of water at its surface. Zinc corrosion in real concrete in the absence of water can be misinterpreted as salt passivity. The presence of oxygen results in an increase of zinc corrosion rate, however at pH 12.6, passivity can occur. It was verified that corrosion products consisting primarily of Ca[Zn(OH)(3)](2)·2H(2)O cannot effectively passivate zinc surface in concrete, even after 1800 h of exposure and zinc, or hot-dip galvanized steel can corrode at an unacceptable corrosion rate (more than 4 µm·a(-1)).