Behavior of aluminum electrodes in electrocoagulation process.

In the present work, electrocoagulation process with aluminum electrodes was investigated. Different operational conditions such as composition of Na(2)SO(4) based solutions, pH and current density were examined in a systematic manner. Their influence on (i) electrode polarization phenomena, (ii) pH evolution during electrolysis and (iii) the amount of Al released (coagulant) was investigated. For this purpose, potentiodynamic tests and electrolyses using different electrochemical cell configurations were conducted. It is mainly found that (i) a minimum Cl(-) concentration of the electrolyte of about 60ppm is required to breakdown the anodic passive film and considerably reduce the cell voltage during electrolysis; (ii) the anodic dissolution efficiency is unit; (iii) the global amount of coagulant (Al(3+)) generated has two origins: electrochemical oxidation of the anode and "chemical" attack of the cathode and (iv) electrolysis with Al electrodes acts as pH neutralization of the electrolytic medium. Taking into account advantage of the pH evolution observed during electrolysis, electrocoagulation tests were performed to treat a synthetic wastewater containing heavy metallic ions (Ni(2+), Cu(2+), Zn(2+)). Removal efficiencies over 98% were reached. Furthermore, our results displayed prominently that an increase of current density notably reduces the treatment duration without inducing a strong increase of the charge loading.