Sodium orthovanadate was tested as a corrosion inhibitor of intermetallic Al2Cu in 1 M H3PO4. The Al2Cu – H3PO4 – Na3VO4 system was studied using the following methods: inductively coupled plasma optical emission spectrometry, scanning electron microscopy with energy dispersive x-ray spectroscopy, x-ray diffraction, electrochemical impedance spectroscopy, polarisation and open circuit potential. It was found that the corrosion rate decreased as the inhibitor concentration increased. The highest inhibition efficiency 99% was obtained when sodium orthovanadate initial concentration was equal to 100 mM, pH = 1.11, due to precipitation of a protective layer of insoluble salt, containing vanadium, phosphorus, sodium and oxygen, on the surface. At pH = 0.76 the protective layer was not formed and inhibition efficiency decreased to 76%. Selective corrosion of the intermetallic phase caused a significant increase of an electric double layer capacitance and decrease of a charge transfer resistance.

Al2Cu phase has been obtained by melting pure metals in the electric arc furnace. It has been found that the intermetallic phase undergoes selective corrosion in the H3PO4 aqueous solutions. Aluminium is dissolved, the surface becomes porous and enriched with copper. The corrosion rate equals to 371 ± 17 g·m–2·day–1 (aerated solution) and 284 ± 9 g·m–2·day–1 (deaerated solution). The surface of Al2Cu phase after selective corrosion was characterised by using electrochemical impedance spectroscopy. It was found that the surface area of the specimens increases with temperature due to higher corrosion rate and is between 2137 and 3896 cm2.

It has been shown that the precipitation of bismuth orthovanadate from a fly ash leachate is a promising method of vanadium recovery. BiVO4 obtained after appropriate heat treatment can be sold as a pigment. The yield of recovery of solubilised vanadium is equal to 68% and the precipitate is free from nickel impurity. The precipitate is insoluble in the solutions with pH ≥ 3. In more acidic media the solubility of precipitate increases with the decreasing pH. The solubility of the precipitate increases also with the increasing concentration of chloride ions.