Description:
<jats:title>Abstract</jats:title><jats:p>In seawater, the application of a cathodic current in a metallic structure induces the formation of a calcareous deposit formed by co-precipitation of CaCO<jats:sub>3</jats:sub> and Mg(OH)<jats:sub>2</jats:sub> on the metal surface. A previous study proved that this electrochemical technique is convincing as a remediation tool for dissolved nickel in seawater and that it is trapped as nickel hydroxide in the deposit. Here, the precipitation of a carbonate form with lead is studied. Pb<jats:sup>2+</jats:sup> precipitation in calcareous deposit was investigated with a galvanized steel electrode by doping artificial seawater with PbCl<jats:sub>2</jats:sub>. Results show for the first time the presence of Pb incorporated in its carbonate form in the calcareous deposit. Trapped Pb content increased with initial Pb content in seawater. Simultaneous doping with Ni and Pb revealed that Ni trapping was favoured by higher current densities while Pb trapping was favoured by lower current densities. Finally, preliminary <jats:italic>in situ</jats:italic> experiments were performed in an industrial bay and validated the incorporation in real conditions of contaminants by precipitation with the calcareous deposit The present work demonstrates that co-precipitation of contaminants under their hydroxide or carbonate form in a calcareous deposit is a promising clean-up device for remediation of contaminated seawater.</jats:p>